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Oncology Scientific Director - IA, NE, MN, ND, SD Job (Gwynedd, PA, US)

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Oncology Scientific Director - IA, NE, MN, ND, SD-MED001898

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Oncology Scientific Director (OSD) is a therapeutic and disease expert who is responsible for facilitating and developing relationships with the Oncology medical/scientific community who have potential interest in participating in Merck research studies (ISTs, Company Sponsored). This position will report to the Team Leader – Oncology Scientific Director (within Global Center for Scientific Affairs).

Primary Activities:

- Support MRL strategy to accelerate Merck’s broader Oncology portfolio through internal candidate development and/or external partnership opportunities.

- Identifies, establishes and maintains collaborative relationships with key investigators, institutions, groups and consortia to identify and address scientific needs and stay abreast of current scientific trends in Oncology

- Support company initiated trials by interacting with primary investigators, assisting in site identification and screenings, and delivering disease education using approved resources

- Conduct peer to peer scientific discussions and maintain a reliable presence with Scientific Leaders to ensure they have a medical contact within Merck.

- Support data generation activities including provision of Merck areas of research interest and ISP process to potential investigators and review of proposals.

- Engage in proactive non-product discussions regarding Oncology scientific issues to assist Merck in obtaining feedback on certain scientific topics of interest to inform Merck’s research activities (e.g., medical practice insights, evidence/data gaps, novel targets and pathways, etc.).

- Demonstrate in-depth knowledge of the assigned disease and therapeutic area(s) through education efforts, including attendance at relevant conferences, workshops and review of key journals.

- Represents MRL at scientific meetings including pipeline booth support, congresses and symposia's, MRL advisory and investigator meetings.

- Fully comply with all company policies and applicable laws, regulations, and ethical standards

Qualifications

Education:

- An advanced degree (M.D., Ph.D. or Pharm.D.) is required with prior experience in the biotech/pharmaceutical or healthcare education environment

Required:

- Ability to travel up to 65% as required per this position.

- The ideal candidate will reside within the position territory: IA, NE, MN, ND, SD

- A minimum of 5 years hematology/oncology experience is required.

- Knowledge of treatment guidelines (NCCN, ASCO, ASH, ESMO, etc.), clinical research processes, FDA regulations, and OIG guidelines

- Excellent interpersonal communication and presentation skills are required.

- Must have the ability to network and partner with important external customers, including Scientific Leaders, investigators, academic institutions, large group practices, NCI Cooperative Group leadership

- Must possess demonstrable effective leadership skills (by example and through accomplishments), and is able to step forward to handle challenges within scope of authority.

- Must demonstrate deep therapeutic competency; stays abreast of trends and new information in the therapeutic/translational science area.

Preferred:

- Clinical trial development experience

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Medical Affairs Generic - Field Based

Job Title:Dir, Medical Affairs

Primary Location: NA-US-PA-Upper Gwynedd

Other Locations: NA-US-South Dakota, NA-US-Iowa, NA-US-Nebraska, NA-US-North Dakota, NA-US-Minnesota

Employee Status: Regular

Travel: Yes, 75 % of the Time

Number of Openings: 1

Senior Scientist, Clinical Research Job (Rahway, NJ, US)

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Senior Scientist, Clinical Research-CLI004194

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


As a Senior Scientist, responsibilities may include, but are not limited to:

- Accountable for the successful leadership, comprehensive clinical and operational planning/feasibility, and execution of a clinical trial. Leads and directs team in key study planning, development and execution elements (e.g., data management deliverables, protocol level plans/timelines, country/site selection, system updates, Investigator Meeting planning and presentations, communication plans, risk identification and mitigation, issue resolution safety and medical monitoring, preparation of status update reports, study closeout activities).
- Leads and directs team for timeline management, risk identification and mitigation, issue resolution.
- Facilitates and collaborates with key internal/external stakeholders (trial team, subsidiary country teams, vendors, committees, etc) in support of clinical trial objectives.
- Accountable for managing any trial specific partners and/or vendors.
- Responsible for authoring of clinical protocols, clinical study reports, regulatory agency update reports, responses to regulatory agencies, and other clinical and regulatory documents. Contribute to the authoring of CTD/WMA subsections.
- Support Clinical Directors in scientific leadership/investigator initiatives including preparation of publications, meeting presentations, etc.

Qualifications

Education:

- A Bachelor’s Degree with a minimum of 11 years in clinical drug development, in the pharmaceutical industry or in the healthcare field (at least 7 years for Bachelor’s Degree in Life Sciences) OR a Master’s degree with a minimum of 8 years in clinical drug development, in the Pharmaceutical industry or in the healthcare field (at least 5 years for Master’s Degree in Life Sciences) OR a PhD with a minimum of 2 years in clinical drug development, in the pharmaceutical industry or in the healthcare field (no experience required for PhD in Life Sciences or related)

Required:

- Understanding scientific process, as well as medical and statistical concepts.
- Understanding of all aspects of clinical development from program planning to regulatory submission.
- Ability to contribute and collaborate with a team including proactive issue identification and resolution.
- Must be able to make independent, timely, data-driven and appropriate decisions.
- Must have excellent, demonstrated oral (including presentation) and written communication, and computer/database management skills.
- Demonstrated project management skills with proven ability to lead cross-functional team and individuals.
- Ability to influence and collaborate internally as well as externally with partners and study-related vendors.

Preferred:

- Minimum of 3 years’ experience in Infectious Diseases areas of pharmaceutical industry preferable.
- Medical writing experience a plus.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Clinical Research (Non-M.D.)

Job Title:Sr. Scientist, Clinical Research

Primary Location: NA-US-NJ-Rahway

Other Locations: NA-US-PA-Upper Gwynedd

Employee Status: Regular

Travel: Yes, 5 % of the Time

Number of Openings: 8

Company Trade Name:Merck

MPS, Specialist (Lean Six Sigma/Merck Production Systems) Job (Wilson, NC, US)

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MPS, Specialist (Lean Six Sigma/Merck Production Systems)-OE/000402

Description

Merck & Co., Inc., known as Merck in the US and Canada and MSD across the rest of the world, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

Champion Lean Six Sigma/Merck Production Systems (LSS/MPS) Initiatives-Educate, communicate and excite the organization on LSS:

- Generate interest for LSS across Wilson, promoting common LSS language across Wilson.

- Leading others and supporting and implementing the MPS/Lean Six Sigma programs as necessary.

- Assist with development of visual workplace and proper execution of tier process

- Encourage a culture of problem solving, continuous improvement, and customer focus

Providing expertise to teams/site including:

- Continuous Improvement concepts such as Six Sigma (DMAIC, Design for Six Sigma (DFSS)), Lean Manufacturing, Change management and High Performing Organization.

- LSS principles of teamwork, methodology, business benefit, innovation and customer focus.

Performance Monitoring and Data Analysis

- Assess business process efficiency and performance.

- Identify LSS financial and non-financial goals.

- Realizing business process improvements and measuring/reporting initiative results.

- Provide consultation to various functions to establish and maintain meaningful metrics

- Manage and report site metrics as requested

Project Support

- Identify opportunities for improvement and support projects through discovery, design and implementation.

- Serve as team member on cross-functional MPS Lean projects.

Benchmarking

- Assist with implementation of best practices across the Wilson site.

- Identify best practices within the site and build network for best practice sharing.

- Share best practices from other Merck divisions and corporate-wide activities.

Continuous Improvement

- Drive scientific problem solving

- Develop and implement standardized work.

- Support creation of visual management tools, 5S, and tier process

- Lead activities to drive operational improvement including OEE, SMED, and TPM.

- Lead transformational change and work on identifying greatest LSS opportunities across the Wilson site.

- Provide leadership for Merck Sigma knowledge management and sharing (i.e. training).

- Recommend and develop training curriculum on specific lean and six sigma tools as needed

- Build and develop personal lean understanding and skill set

Work with MPS sponsors/team leader supporting continuous improvement projects through mentoring and coaching

- Work directly with sponsors to support change initiatives.

- Active participation with continuous improvement team leaders

- Serve as team member for critical site projects

Perform other duties as assigned.

Qualifications

Education:

- Required: BS/BA

Required Experience:

- Functional experience in operations, technology/engineering, supply chain, or quality. (1+ years)

Preferred Experience:

- Green Belt or equivalent  

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: OE/Six Sigma

Job Title:Spclst, Business Consulting

Primary Location: NA-US-NC-Wilson

Employee Status: Regular

Travel: No

Number of Openings: 2

Shift (if applicable): 1st

Company Trade Name:Merck

Production Planner Job (Boxmeer, NL)

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Production Planner-MAT000314

Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.
Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


MSD has a workforce of almost 4500 in the Netherlands at three main sites.

MSD. Be well. For more information, visit our website: www.werkenbijmsd.nl

Production Planner
The role is based at our Animal Health (AH) facility in Boxmeer, which is part of our global Manufacturing Division AH network. We manufacture and pack animal health products.

The Integrated Process Team (IPT) Live is responsible and accountable for all resources that are required to produce viral live vaccines (antigens & FPU) compliant and according to Good manufacturing practices (GMP) standard. The scope of this IPT contains: Tissue Culture Boxmeer and De Bilt, Sphereon, Central Filling & Freeze Drying and the supporting activities Planning, Maintenance & Reliability and Improvement.

As Production Planner you are responsible for Production Planning, Supply Chain Planning, Operational Planning and supporting activities.

For Production Planning you do end-to-end planning and -coordination of the supply chain. You define long range production and capacity plan for the site, 3-6 months production plan, solve capacity constraints and defines supply scenarios
Annual budget volumes (purchase and manufacturing) are determined by you

Communication around supply issues in the network is part of Supply Chain Planning
as is scenario planning and preparing resolution plans in case of supply-demand imbalances. Collaboration with Marketing for non-forecasted external sales and MSD production departments for intercompany sales is also part of Supply Chain Planning.

For Operational Planning you translate the monthly plan in a weekly production program in close cooperation with the operational coaches within the IPT to optimize customer service, overall working capital and activity level of the IPT. You allocate batches to process orders and release orders to the Operational Coach in the IPT for day to day planning activities and monitor their scheduling adherence
You allocate batches to process orders and release orders to the IPT-Outbound / Packaging Department. You monitor and prioritize Quality Control-lab analysis and Quality Assurance-release activities.

Supporting Activities consist of planning and monitoring product transfers. Internal between IPT's and external with BTS and Marketing. You follow up on Phase out process and new Products
You perform annual revision of supply chain policies like campaign size, order quantities and lead times throughout the supply chain and implementation at IPT level. Annual supply chain risk assessment to set the safety stock levels at the decoupling points are part of your responsibility. You are responsible for the stock levels at the decoupling points (target, lead times, safety stock level) + material availability.
You inform stakeholders on short dated and unsalable stock and initiate the D&O process and follow up on the strategic and anticipation stock procedures.

Qualifications

- HBO in Supply Chain Management or equivalent qualifications

- Minimum of 5 years of experience in supply chain management, preferably within Biological / Pharmaceutical Manufacturing

- Communicator in the network

- Experience with usage metrics to make problems visible

- Good understanding of ERP, Demand planning and MRP

- Willing to certify for or possessing a Green Belt Degree

- Passion for Lean / Continuous Improvement and willing to make personal change

- Customer focused, process oriented and data driven

- Good command of writing and speaking in Dutch and English

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job: Materials Planning/Scheduling Job Title:Production Planner

Primary Location: EMEA-Netherlands-NB-Boxmeer

Employee Status: Regular

Number of Openings: 1

Executive Director, Business Development, Search & Evaluation Job (San Francisco, CA, US)

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Executive Director, Business Development, Search & Evaluation-BUS001315

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The West Coast Innovation Hub within the Business Development & Licensing organization is a fully functional business development organization focused on driving deals with West Coast biotechnology companies and academic centers. The West Coast Innovation Hub will operate out of Merck’s new Mission Bay offices in San Francisco, CA, have responsibility for accessing life sciences innovation for Merck in California, Oregon and Washington and accountable for elevating the visibility and profile of Merck within the life sciences communities on the West Coast.

The Executive Director, Business Development, Search & Evaluation will be a highly experienced business development professional with a track record of completed buy-side biotechnology transactions. The Executive Director will have responsibility for finding innovative therapeutics or platform technologies that could impact Merck’s pipeline, leading scientific evaluation teams to complete due diligence activities, presenting opportunities to Merck Research Laboratories (MRL) senior leadership and then working within deal-teams to negotiate and execute transactions. The Executive Director will also coach and mentor other Search & Evaluation Directors and help to manage the portfolio of opportunities under management by the West Coast Innovation.

Specific responsibilities include and are not limited to the following:

- Acting as Merck’s spokesperson and scientific prospector for identifying new research collaborations, preclinical compounds, clinical compounds and/or technologies on the West Coast and the surrounding region through licensing, acquisition, collaborations, co-development agreements, and strategic alliances.

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Performing scientific evaluation of pre-clinical proof-of-concept human health licensing, collaboration and acquisition projects.

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Working with Merck Research Laboratories scientific leadership in applicable Therapeutic Areas and line functions in setting and challenging licensing strategy.

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Guiding the team that scientifically executes the therapeutic area licensing strategy by leading the Search & Evaluation component of the overall licensing process.

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Leading the cross-functional scientific teams that are responsible for due diligence and scientific negotiations/approvals on major licensing projects.

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Mentoring more junior Search & Evaluation professionals to ensure quality and consistency in the Search & Evaluation process and providing for development opportunities for junior staff.

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Collaborating with Transactions team members, Alliance Managers and colleagues in the Early Assessment Team and the Late Assessment Team to ensure alignment and to ensure proper input is received from subject matter experts across Merck.

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Elevating the profile of Merck as a collaborator by designing programming and making presentations on behalf of Merck at industry networking events, scientific conferences, and other venues.

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Communicating Merck's licensing desires to internal and external stakeholders, while remaining open to identifying and advocating for new game-changing opportunities.

The position manages a large portfolio of complex projects and is responsible for timely responses to potential partners (large, mid-sized, and small pharma; biotech; academia; and government) and regular communication across the organization regarding the progress of partnering opportunities. The Executive Director partners with transactions professionals and scientific colleagues to progress deals to completion. Throughout the search, evaluation, and execution process, the Executive Director provides assessments and updates to Senior Management and ensures that there is a sufficient flow of quality opportunities to maintain the health of the Merck pipeline. He/She helps to coordinate the portfolio of Search & Evaluation projects and coordinates activities between the Hub and others in BD&L.

Qualifications

Education:

*
Required: Graduate degree (including Masters level) in a Life Sciences discipline

- Preferred: MD or PhD in a Life Sciences discipline and MBA or JD

Required Experience:

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Minimum of (8) years of experience in Biotech or Pharmaceuticals industry, with a minimum of (5) years of applicable business development experience

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Broad-based scientific knowledge across human health therapeutic areas

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Understanding of basic science technologies as applied to medical targets

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Strong networking, organizational, administrative, analytic, computing skill and sound judgment

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Superior written and oral communication skills

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Ability to influence decisions or issues that have broad business impact

- Expertise in leading edge business development practices and techniques.

Preferred Experience:

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Minimum (10) years experience in Biotech or Pharmaceuticals industry, with a minimum of (7) years of business development experience and a demonstrable record of sourcing and closing buy-side transactions

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Business Consulting

Job Title:Executive Director, Business Consulting

Primary Location: NA-US-CA-San Francisco

Employee Status: Regular

Travel: Yes, 20 % of the Time

Number of Openings: 1

Company Trade Name:Merck

Principal Scientist - Assay Support Job (Palo Alto, CA, US)

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Principal Scientist - Assay Support-MOL000319

Description

Merck & Co., Inc., known as Merck in the US and Canada and MSD across the rest of the world, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We are seeking an experienced and highly motivated Principal Scientist with hands-on experience in assay development and screening to support antibody discovery programs at the Merck Biologics unit in Palo Alto. Responsibilities will include, but are not limited to:

- designing and executing early protein and cell-based screens to support biologics programs across multiple therapeutic areas.

- being a hands-on manager of direct reports and is expected to work at the bench as needed

The ideal candidate must have:

- solid hands-on experience with biochemical, biophysical (SPR) and cell-based assay development utilizing multiple technologies.

- Previous experience screening antibodies (crude and purified) to characterize binding and functional activity is a must.

- The candidate is expected to be up-to-date on advanced technologies for antibody discovery screening and actively apply new concepts as appropriate to continuously improve functional area capabilities.

- The ideal candidate would also have prior experience leading antibody discovery projects either internally or externally.

Qualifications

Education:

- PhD with a minimum of 8 years of related experience or a MS with a minimum of 10 years of related experience in cell biology, immunology, biochemistry or a related discipline of relevant experience in antibody discovery

Required:

- Expertise in high-throughput protein and cell-based assay development and screening in a pharmaceutical or biotechnology setting

- Expertise in Biacore based assay development and screening

- Experience with antibody production from hybridomas

- Ability to manage multiple projects simultaneously

- Strong written and verbal communication skills

- Previous experience managing direct reports with a proven track record of developing careers

Preferred:

- Experience working with external vendors and collaborators in a fee-for-service and/or co-development capacity

- Experience working with liquid handling workstations

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​

*LI-HC1


Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Molecular Discovery - Biologics

Job Title:Prin. Scientist, Molecular Discovery

Primary Location: NA-US-CA-Palo Alto

Employee Status: Regular

Travel: Yes, 5 % of the Time

Number of Openings: 1

Shift (if applicable): 1st

Hazardous Materials: Standard biohazardous material as routine part of antibody discovery

Company Trade Name:Merck

Senior Business Analyst Job (APAC-Korea, Republic of)

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Senior Business Analyst-BUS001427

Description

1) Job Title : Senior Business Analyst

2) Department : IT, MSD Korea

3) BPL : P3/400 (Kwa Jang ~ Cha Jang)

4) Report to : IT Account Manager

5) Job Objective

Performs and delivers the IT services to provide the technical advantages for the business by understanding the business processes and their needs mainly related multi-channel and digital marketing

6) Main R&R

- Work within Korea IT team and with Global Hub, partners to deliver multi-channel and digital marketing related IT capabilities to business clients in our Commercial business areas

- Facilitate discussions/workshop with business partners to understand current and future state business processes and requirements, Formulates and defines scope and objectives pertaining to the IT service

- Drive business process design through the application with SDLC, Governance procedures and other operational excellence techniques. Complete all compliance documentation for system release

- Participate in strategic programs that will incorporate commercial solutions as part of multi-channel future

- Develop best practice recommendations and lead continueous innovation in digital marketing capabilities

- Keep abreast of new technologies, methodologies, industry practices and standards

- Devises or modifies procedures to resolve problems considering computer equipment capacity and limitations

7) Working Relationship

 Internal : Regional or Local IT Client Service, SFE, MSE, MCM

 External : IT Vendors

Qualifications

8) Qualification

Functional Knowledge : IT Solutions (BI, CRM, MCM, Applications Development, and IT architecture), Excellent application life cycle knowledge, including design, development and integration , maintaining security and quality standards and achieving an optimal and cost/effective allocation of internal and external resources.

Skills : Technical skills in the IT systems like BI, CRM, MCM and applications development, Project management skills, software design and development skills, Experienced in developing business cases

Leadership Behaviors : Focus on Customers and Patients, Foster Collaboration, Drive Results

Others : Strong analytical thinker and problem solving skills with strong experience in digital marketing

Education : BS Degree in Computer science, Information systems or Marketing

Experience : 2+ Years of relevant experience in manaing IT delivery activities or supporting a sales and marketing environment

English : WOrking confident

Job: Business/Technical Analysis Job Title:Senior Business Analyst

Primary Location: APAC-Korea, Republic of

Employee Status: Regular

Number of Openings: 1

Company Trade Name:MSD

Quality Lab Supervisor Job (Elkton, VA, US)

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Quality Lab Supervisor-QUA004305

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Description:

The Laboratory Manager, In-Process and Water, reports to the Associate Director, Elkton Quality Operations Analytical with indirect reporting to Associate Director, Elkton Quality Operations Microbiology, and will have direct responsibility for all QC In process and Production Water System testing.

Responsibilities:

- Directly leads activities in the Laboratory associated with production In Process Testing, Water Testing, and Environmental Monitoring Plate Reads.

- Collaborate with multiple separate Integrated Production Teams and provide support in the area.

- Interacts with regulatory agencies and provides support to all audits.

- Manages team of approximately 8 direct reports, including hourly and salaried.

- Covers shift when required.

Qualifications

Education Requirements:

- Bachelor's degree in Chemistry, Biology, Microbiology or related science.

Required:

- Minimum of 5 years demonstrated expertise in supporting Aseptic Processing, Biologics or Vaccine Manufacturing.

- Laboratory experience required.

- Demonstrated ability to collaborate and work in a team environment, build talent and manage the development and necessary change in today's manufacturing world.

- Contemporary knowledge of GMPs is required.

- Strong compliance mindset.

- Good verbal and written skills.

- Must have computer skills with Microsoft systems.

Preferred:

- Microbial and analytical assay knowledge.

- Managerial experience.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Quality Operations

Job Title:Mgr, Quality

Primary Location: NA-US-VA-Elkton

Employee Status: Regular

Travel: No

Number of Openings: 1

Hazardous Materials: Laboratory Chemicals

Company Trade Name:Merck

Submissions Sr. Publisher/Specialist Job (Rahway, NJ, US)

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Submissions Sr. Publisher/Specialist-REG002040

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Global Submissions Publishing (GSP) works closely with various stakeholders to ensure the timely completion of submission assemblies that adhere to both regulatory health authority and Merck guidelines for electronic/hardcopy submissions. The incumbent will support global process; executing end-to-end submission assembly which includes publishing, quality control verification, finalization and delivery. This requires collaborative interaction with component providers and submission managers to ensure quality, right first time output and timeliness. The incumbent will assume the role of lead publisher for larger, complex submissions (e.g. original marketing applications), which will include coordination of all publishing-related activities and delegation of activities to other publishers. Additionally, the incumbent will take the lead in the development of administrative documentation, provide inter-departmental and/or external stakeholder mentoring, and play an integral role in the testing and implementation of new systems, tools, and processes.

Primary responsibilities will include the following:

Publishing Support:

- Work closely with submission managers to lead the production of high quality submission assemblies utilizing submission-ready documents that adhere to internal and external electronic submission guidelines

- Ensure submission assemblies meet the level of technical integrity required for Merck and health authority validation tools

- Assume the lead for training/mentoring internal and external publishing staff

- Assist submission project teams with the identification of submission ready content requirements and applicable timeline milestones for execution of right-first-time submission assemblies

- Identify, assess and actively resolve or escalate where necessary any risks or issues that could impact the successful completion of regulatory submissions

- Assist with departmental metrics by tracking status of projects, day-to-day production activities, and publishing anomalies

Administrative Support:

- Assume the lead role in the development of publishing processes and documentation, including user acceptance testing for new and updated publishing tools. Delegation of these project activities to publishers within the department as needed.

- Assume the role of subject matter expert for specific functions or processes, interacting and mentoring both within the department and with external stakeholders

- Evaluate activities and business processes, identify areas in need of improvement and take the lead in investigating potential solutions or new ways of working

Qualifications

Education:

- Minimum of Bachelor’s degree

Required:

- 5 years of regulatory publishing experience

- In depth working knowledge of industry standard publishing systems and desktop applications including MS Word and Adobe Acrobat Professional

- Effective time management and organizational skills to efficiently manage multiple time-sensitive assignments simultaneously

- Demonstrates deep understanding of the business value of quality and compliance, and the implications and risks of non-compliance. Adjusts behaviors to drive high quality deliverables

- Demonstrates the ability to independently solve complex problems that arise within job responsibilities and expectations, and takes a new perspective using existing solutions

- Effectively communicates difficult issues both verbally and in writing to build alignment around a complex situation

- Flexibility to adapt to a changing environment, keeping current with new and updated processes and procedures

Preferred:

- 8 years of regulatory publishing experience

- Expertise with the Liquent InSight Publisher application

- Expertise with industry standard electronic document management system

- Experience with project management and leading teams

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Regulatory Affairs Generic

Job Title:Sr. Spclst, Regulatory Affairs

Primary Location: NA-US-NJ-Rahway

Employee Status: Regular

Travel: Yes, 5 % of the Time

Number of Openings: 3

Shift (if applicable): 1st

Company Trade Name:Merck

UX Researcher Job (Singapore, SG)

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UX Researcher-SER000694

Description

• Work cross-functionally with design, product management, analysts, engineering and marketing to strategize, prioritize, plan, and execute on research initiatives.
• Help our UX Designers build and refine user experiences that determine how people interact with our products on a day to day basis.
• Conduct research using a wide variety of qualitative and quantitative methods and interpret analysis through the lens of UX and HCI.
• Generate deliverables that are thorough, concise, and well-designed including research reports, personas, scenarios, conceptual models, sitemaps, functional flows, and annotated wireframes.
• Ideate and execute on tactical usability assessment for ongoing projects using both traditional and Lean UX methodologies, as well as participating in strategic forward-looking research as necessary.
• Coordinate with other departments in the organization to uncover new customer insights by combining quantitative and qualitative research and product usage data.
• Mentor and advise individuals in conducting independent user research.
• Contribute user experience best practices and act as an experience evangelist, advocating for our members and representing their needs and perspectives to the entire organization.

Qualifications

• Passionate about research, data and user experience.
• Bachelors or advanced degree in HCI, Cognitive Science, Design or related field.
• Have 3+ years of work experience in an applied user experience research preferred.
• Experience developing customer insights using a combination of qualitative research and quantitative data analysis is highly desired
• Experience with mobile and multi-device UX testing
• Must be organized, able to think beyond what is asked for, act independently, and juggle multiple projects and competing priorities in a fast-paced environment
• Have experience in Agile (iterative) processes.
• Experience with survey research (questionnaire design, sampling, analysis) preferred
• Demonstrated ability to show initiative and work as part of a highly collaborative team: able to listen effectively, respectful of others perspectives and contributions, and able to both offer and accept feedback openly
• Successful record of influencing product design by providing insight into customer behaviors and preferences through effectively communicated findings and potential design solutions inspired by the findings
• Have excellent communication, presentation, and interpersonal skills.
• Portfolio of relevant research and design work is required with application for consideration

Job: Service Delivery/Management Job Title:UX Researcher

Primary Location: APAC-SG-Singapore-Singapore

Employee Status: Regular

Number of Openings: 1

Stagiair(e) (Haarlem, NH, Nederland)

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Stagiair(e)-ADM006961

Omschrijving
MSD is op zoek naar een enthousiaste en ambitieuze:

Stagiair(e)

ten behoeve van de afdeling: Quality Assurance Systems

MSD Haarlem is een farmaceutisch bedrijf waar ongeveer 800 medewerkers werkzaam zijn. MSD Haarlem produceert, verpakt en verzendt geneesmiddelen naar meer dan 140 landen.

De afdeling Quality Assurance Systems (QA-S) levert een bijdrage aan het succes van MSD door het borgen en toetsen van de kwaliteit van alle activiteiten op de site en de producten die geleverd worden.

De werkzaamheden

Vendor Management

- De processen van het verwerken van vendor changes (veranderingen in bijvoorbeeld processen bij een leverancier) in de diverse systemen in kaart brengen. Hiervoor verbetervoorstellen uitwerken en na goedkeuring doorvoeren;

- Uitvoeren van de plannen voor de harmonisatie van Vendor Management formulieren en documenten

Quality Risk Management (QRM)

- Meedenken en ondersteuning bieden bij het uitrollen van het nieuwe QRM op de site.

Position papers opstellen

- De Site Lead Auditor en SSE’s ondersteunen door het opstellen van position papers op diverse onderwerpen t.b.v. externe inspecties

De beschreven werkzaamheden vormen de basis en zullen na een goede inwerk- en leerperiode zelfstandig uitgevoerd worden. Op eigen initiatief of door vraag vanuit de organisatie kunnen deze worden aangevuld met andere projecten en/of taken.

Kwalificaties
Wij zoeken iemand met:

- Een bijna afgeronde masteropleiding

- Affiniteit met de farmaceutische industrie

- Een leergierige, zelfstandige en kritische houding

Stage:

- De stage start per 1 september en duurt ten minste 4 maanden (duur wordt in overleg vastgesteld)

- De stage is bij voorkeur full time, maar minimaal 4 dagen per week

Wij bieden:

- Een breed georiënteerde stageplaats, die je in staat stelt om met veel aspecten van het vakgebied kennis te maken en daar ervaring in op te doen, met veel ruimte voor eigen initiatief.

- Een uitdagende en dynamische leeromgeving met veel ruimte voor persoonlijke ontwikkeling.

- Goede begeleiding door een ervaren stagebegeleider

- Een stagevergoeding van € 470,- bruto per maand (op basis van een 40-urige werkweek)

Informatie & Sollicitatie:
Heb je belangstelling voor deze stageplaats stuur dan een email uiterlijk 17 juli met je sollicitatiebrief en CV naar Eline Claase (HR) via het volgende emailadres: info@msd.nl (A.U.B. t.a.v. Eline Claase in het onderwerp vermelden)

Voor meer informatie over de vacature kun je contact opnemen met Rianca Jak via +31 235153501
Functie: Administratieve diensten generisch Job Title:Stagiair(e)

Primaire locatie: EMEA-Nederland-NH-Haarlem

Status werknemer
: Vast
Aantal vacatures: 1

Regional Service Lead Job (Singapore, SG)

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Regional Service Lead-SER000742

Description

Reporting to the AMS AP Regional Service Delivery Lead, has responsible for Support and Operations of manufacturing and research business applications in Asia Pacific. This position is going to require a strong change management component, due to the implementation of the managed service model and a significant level of maturity, of the manager, in this position.

The incumbent will have the following responsibilities:

1) Demand Management: Drives business-IT outcomes; manages communications and expectations with business client; simplifies IT engagement by serving as primary point of interaction and contact with the business.

2) Supplier Management: Participates in governance meetings with Vendor Partner, including negotiations in contract issues, new services and attend regular Service Level reviews. Manage the global and the local suppliers which provide MS&O support for the legacy systems in the scope of the AMS organization. This person has to participate in the governance defined for these agreement, guarantee the service levels, at the same making time, make sure that the supplier is fully aligned and compliance with the Merck policies.

3) Service Management: Manages a defined service unit, including team design, workflow and procedures, aggregate demand management, estimating, work assignments, service agreements, and sourcing specific to the service; manages annual continuous improvement process; provides early warning to the executives regarding degrading or missed service levels; collaborate with business and solution architect functions as needed; decides whether an escalated incident needs to be resolved by implementing an emergency change or by continuing the resolution of the incident within the Incident Management process.

4) People management: Manages the MMD, MRL and AH IT team distributed across APAC; builds a strategic IT capability for the client through strategic staffing, and organizational development, as well as employee recruitment, retention and development.

5) Financial management: Managed the budget allocated in the countries where the AMS has footprint, including the P&B and Services distributed in the countries where AMS has operations.

Qualifications

Education Level:

• The candidate should have Computer Engineering degree with 8+ years in providing functional and technical leadership in the pharmaceutical manufacturing and R&D space, as well as in supporting the critical apps which maintain the business process to guarantee the continuity of the business operations with zero or minimal systems issues.

• Extensive background in IT management, profound knowledge of support methodologies (e.g. ITIL).

Experience/Technical Skills:

• Excellent communication skills, able to influence at all levels of the organization
• Good negotiation English level. Fluent in English, in both verbal and written communication
• Experience in IT operations in large and critical systems. International experience managing a multicultural team.
• High problem management skills, with a very good business impact understanding in pharmaceutical manufacturing and research functions, and ability to make fast decisions related with the production environment.
• Able to make budget decisions under limited supervision with high level information and under tight deadlines and pressure. Management of the team distributed in the geography under his/her responsibilities. Contractual decisions about the local and regional contracts in close collaboration with Procurement.
• Solid ability to create positive relationships at a senior level across different groups & teams. Strong communication skills are required in order to communicate with all levels within the organization.
• Able to work on own initiative taking into account the need for flexibility due to changing priorities and working to tight deadlines
• Ability to accomplish objectives while working with the Global MS&O team, IT divisional leaders and country IT departments.
• Strong change management component is required, due to the implementation of the outsourcing strategy. This new model is going to have organizational changes with people impacted

Job: Service Delivery/Management Job Title:Assoc. Dir, Service Delivery/Management

Primary Location: APAC-SG-Singapore-Singapore

Employee Status: Regular

Number of Openings: 1

Company Trade Name:MSD

Medical Affairs Director, Hospital Job (Los Angeles, CA, US)

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Medical Affairs Director, Hospital-MED001931

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Field-Based Medical Director, Hospital is a therapeutic and disease expert who develops on-going professional relationships with healthcare practitioners to help achieve positive health outcomes for patients. The incumbent provides accurate information about Merck products, clinical science, and quality management in a balanced and credible manner consistent with the regulatory environment and Merck’s ethical standards. The Field-Based Medical Director serves as a resource for the USMA management team on strategic planning and provides mentoring for other team members.

Key responsibilities include and are not limited to the following:

- Develop professional relationships and communicate with national and regional thought leaders to ensure access to medical and scientific information on Merck products and areas of therapeutic interest.

- Conduct peer to peer scientific discussions and maintain a reliable presence with those thought leaders to ensure they have a medical contact within Merck.

- When needed, serve as a resource for the identification of potential investigators for consideration for participating in phase II-IV clinical development programs.

- Provide areas of interest and general information regarding the Merck Investigator Study Program process.

- Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training partner.

- Attend scientific and medical meetings and support development of post-meeting deliverables.

Territory covers: Los Angeles, CA, Northwest Corner

This position requires 50% travel.

This Position Reports to: Micheal Cmiel.

Qualifications

Education:

- Required: MD, PharmD, or PhD

Required:

- Minimum of (3) years’ experience and proven therapeutic competence in the disease area

- Clinical (patient care) or deep research experience in assigned therapeutic area(s) beyond that obtained in the terminal degree program

- Capable of conducting doctoral level discussions with key customers

- Strong customer focus

- Business and market knowledge, including quality management.

- Excellent interpersonal, communication, and networking skills

- Must possess a thorough understanding of the FDA, OIG, HIPPA and other ethical guidelines relevant to the pharmaceutical industry

- Must be able to organize, prioritize, and work effectively in a constantly changing environment

- Strong working knowledge of Microsoft Office Suite (Outlook, Word, PowerPoint, Excel, Access).

- Travel 50%

Preferred:

- Field-Based Medical experience

- Clinical Research experience

- Demonstrated record of scientific/medical publication

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Medical Affairs Generic

Job Title:Director, Medical Affairs

Primary Location: NA-US-CA-Los Angeles

Employee Status: Regular

Travel: Yes, 50 % of the Time

Number of Openings: 1

Hazardous Materials: No

Company Trade Name:Merck

PSR-DR-HZ Job (Hangzhou, CN)

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PSR-DR-HZ-DIR012661

Description

Functional Area Definition Responsible for closing direct sales ofproducts and/or services in order to meet individual/team quotas andthe organization's business objectives. Creates, monitors and reviseslead generation plans to generate a substantive sales opportunitypipeline. Responsible for inbound and/or outbound sales calls directlyfrom/to prospective and/or existing customers. Responds to customerquestions and takes orders. Effectively builds rapport with customersby probing for needs and recommending appropriate solutions. Achievesmonthly, quarterly, and annual sales objectives, while ensuring theoptimum customer experience and satisfaction by following establishedprocesses and procedures. Job Family Definition Promotes and sellstechnical and/or nontechnical products and/or services and solutionsdirectly to current and new end customers. Informs customers of newproduct/service introductions and prices for such. Creates, monitorsand revises lead generation plans to generate a substantive salesopportunity pipeline. Produces revenue in line with the organization'sand individual targets/quotas. Sells a portfolio of products and/orservices including more than one of the job sub-groups below.

Qualifications

Functional Area Definition Responsible for closing direct sales ofproducts and/or services in order to meet individual/team quotas andthe organization's business objectives. Creates, monitors and reviseslead generation plans to generate a substantive sales opportunitypipeline. Responsible for inbound and/or outbound sales calls directlyfrom/to prospective and/or existing customers. Responds to customerquestions and takes orders. Effectively builds rapport with customersby probing for needs and recommending appropriate solutions. Achievesmonthly, quarterly, and annual sales objectives, while ensuring theoptimum customer experience and satisfaction by following establishedprocesses and procedures. Job Family Definition Promotes and sellstechnical and/or nontechnical products and/or services and solutionsdirectly to current and new end customers. Informs customers of newproduct/service introductions and prices for such. Creates, monitorsand revises lead generation plans to generate a substantive salesopportunity pipeline. Produces revenue in line with the organization'sand individual targets/quotas. Sells a portfolio of products and/orservices including more than one of the job sub-groups below.

Job: Direct Sales Generic Job Title:Customer Rep., Sales

Primary Location: APAC-CN-33-Hangzhou

Employee Status: Regular

Number of Openings: 1

Company Trade Name:MSD

Benelux Companion Diagnostic Lead Job (Haarlem, NL)

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Benelux Companion Diagnostic Lead-MAR005504

Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.
Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The position
The CDx Lead will be responsible for localizing and implementing the project-related biomarker and CDx strategy for an investigational product being evaluated in Non Small Cell Lung Cancer plus New Indications. The Country Cluster CDx Lead is a key member of the Benelux Oncology teams for this promising investigational product within a new class of drugs intended for patients suffering from malignant cancer diseases. Utilization of this drug is expected to be associated with an approved CDx, and there is a need to implement a bespoke biomarker strategy, given the anticipated impact of the CDx on drug adoption. The individual main responsibility will include the go-to-market and CDx commercialization plan for the CDx in the Benelux region. At the same time, the CDx lead is accountable for ensuring full integration of the CDx launch plan within the overall product strategy. He/She will be driving strategic choices, adaptation and local implementation of the CDx launch readiness and excellence plan according to country needs and requirements. The ideal candidate should have a strong understanding of the CDx, translational medicine as well as Oncology field. The candidates will report to the Business Unit Oncology Lead Netherlands, and be based in Haarlem (BeNeLux).

Key accountability
Customize and implement, through appropriate leadership, direction and action, agreed global/regional biomarker and CDx strategies and commercialization plans by

- Taking the lead in ensuring that teams develop informed and appropriate biomarker tactical plans that are suitable for NSCLC, including emerging biomarkers and technologies for new indications

- Providing markets with guidance on local implementation in alignment with the global and regional CDx teams

- Acting as primary Point-of-Contact for the global and regional CDx teams to represent the voice of the Mid-Europe Region

- Appropriately engaging with academic and external industry based experts and providers who are focusing on translational medicine and CDx deployment (scientists, oncologists, pathologists, lab technicians, pulmonologist, thoracic surgeons)

- Coordinating Medical Education, training and coaching activities for key stakeholders (pathologists, lab technicians)

- Securing capacity and quality via appropriately establishing centers of excellence for biomarker testing and implementing biomarker testing initiatives including QC/QA programs

- Taking the lead on monitoring of biomarker and CDx activities, coordination of data collection and interpretation, and preparation of the results for informed decision making

- Managing the alliance with Diagnostics partner (i.e. DAKO)

Qualifications

- Bachelor (minimum requirement); Masters or PhD preferred

- You have in-depth knowledge and experience in biomarker implementation and CDx commercialization with preferred experience in Oncology (e.g. launch preparation and roll-out of a CDx-supported Oncology brand)

- You have the ability to manage teams and key external stakeholders, to influence without authority, and to create and carry out action plans in matrix cross-functional team structures

- You exhibit strong leadership, problem solving, project planning, teamwork, analytical, and written/verbal communication skills

- As this is an above-country position, you should also be willing to travel within the region and work cross-culturally

- Fluently Dutch and English, French is a pré

Application
If you are interested in this challenging role, you are requested to apply online by uploading your resume and application letter in English.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job: Marketing Operations Job Title:Benelux Companion Diagnostic Lead

Primary Location: EMEA-Netherlands-NH-Haarlem

Employee Status: Regular

Number of Openings: 1

Company Trade Name:MSD

Associate Principal Scientist.- Downstream Processing Job (West Point, PA, US)

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Associate Principal Scientist.- Downstream Processing-PRO013042

Description

Description:

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Process Development and Commercialization (Biologics) is responsible for the commercialization of biological processes from Phase III through launch and transfer to commercial supply network. Activities include process development, scale-up and optimization, interfacing with a network of facilities for product manufacturing and subsequent validation and filing documentation, and transfer to supply network. PDC is part of the Merck Manufacturing Division.

Under the general scientific and administrative direction of the Director of PDC and working in conjunction with internal and external partners, this individual will support late stage bulk process development, characterization, technology transfer, clinical manufacturing, and validation studies associated with the development and implementation of bulk processes, systems and facilities related to therapeutic proteins. The individual will demonstrate scientific, experimental and tech transfer skills focusing on cell culture processing.

Responsibilities:

- Responsible for development and characterization of late stage protein purification processes suitable for PPQ, licensure, and commercial manufacturing

- Able to work independently and lead multidisciplinary teams

- Responsible for managing outsourced process development and characterization activities at CMO/ TPO

- Responsible for development, execution, and documentation of process characterization studies of downstream processes using advanced skills in QbD, DOE, PAT, and data analysis

- Responsible for development of optimized post-launch process

- Responsible for tech transfer of downstream processes for production of therapeutic proteins including drafting of technical reports and manufacturing documentation. Interfaces with early development, technical operations, and manufacturing departments to facilitate transfer of manufacturing processes

- Responsible for downstream related CMC enabling documentation

- Project management and participation in cross-functional/global CMC teams

- Manages and is responsible for the quality level of downstream related process development studies and documentation

- Participates, as the protein purification subject matter expert, in regulatory inspections and is experienced with the cGMP and regulatory guidelines

- Identifies new technologies and works to implement new platforms with cross-functional early and late stage development teams

Qualifications

Education Requirements:

- PhD (or equivalent experience) in biological sciences, biochemistry, or biochemical engineering

Required:

- Minimum of 5 years relevant experience in managing biotechnological development projects

- Relevant purification development and protein chemistry experience

- Proven strong scientific, project, and people management skills

- Strong communicator and ability to build bridges between groups and organizations.

- Excellent analytical and technical skills

- Demonstrated initiative, and innovative process-oriented thinking within a team environment

- Knowledge of regulatory and quality guidelines, and knowledge on CTA/ and CTD format for IND/ BLA/ MAA submissions preferred

- Experience in manufacturing sciences preferred

Preferred:

- Experience with supporting regulatory filings for US and worldwide markets

- Knowledge of regulatory and quality guidelines, and knowledge on CTA/ and CTD format for IND/ BLA/ MAA submissions

- Experience in manufacturing sciences

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Process Engineering

Job Title:Assoc Prin. Scientist, Engineering

Primary Location: NA-US-PA-West Point

Other Locations: NA-US-NJ-Kenilworth

Employee Status: Regular

Travel: Yes, 15 % of the Time

Number of Openings: 1

Shift (if applicable): 1st

Hazardous Materials: Standard laboratory chemicals

Company Trade Name:Merck

EMEA B&AR Analyst (French Market) Job (Dublin, IE)

$
0
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EMEA B&AR Analyst (French Market)-SHA000295

Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Reporting to the Order to Cash (OtC) Billing and Accounts Receivable Manager, the OtC Collections Analyst is responsible for the following:

- Collections Calls in line with the requirements of the French market to reduce aged debt, maximising collection effort and collating high quality dispute/ deduction information.

- Working to collection targets

- Preparation & approval of the blocked orders for the market

- Assist in maintaining unallocated cash within agreed limits

- Reporting on Month end KPI's where necessary.

- Conforming to Internal Manual controls process.

- Supervise, lead and coach the rest of the French team located in Bucharest.

The primary activities that you will be performing include:

- Ensure SLA’s and KPI’s are met.

- Meet weekly/monthly collections targets

- Request payment remittance from customer to provide to Cash Applications Team

- Daily contact by phone with customers to establish payment date

- Collect progress and escalate high quality dispute information as required in accordance with escalation policy.

- Assist in the preparation of management reports in line with requirements.

- Ensure that the collections process are followed and in adherence with SOX.

- Be proactive and innovative with ideas to improve service / deliverables.

- Attend meetings to discuss debtor performance and address issues as required.

- Produce monthly statements to send to external customers in line with clients SOX processes.

Qualifications

- Third Level Business Degree

- Fluent English and French (business Level fluency oral and written).

- A minimum of 2 years of demonstrated work experience within the OtC area and a basic understanding of cash application processes and technologies an advantage.

- Experience working in an organization providing services across multiple markets or geographies.

- A minimum of one year of experience working with SAP.

- High degree of integrity and personal ethics in implementing corporate policies and procedures

- Effective team player with collaborative focus, flexible, enthusiastic, innovative and proactive

- Attention to detail with a good organizational & time management skills

- Must be able to work in a fast-paced, dynamic environment, under pressure, and with a high degree of professionalism

- Must be comfortable in an environment of changing technologies and processes, and demonstrate flexibility in adjusting to new ways of working

- Experience working in a SOX404 environment.

- Strong oral and written communication skills.

- Flexible work arrangements will be considered based on business needs.

- Strong interpersonal skills both oral and written with very good telephone skills.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job: Shared Services Job Title:EMEA B&AR Analyst (French Market)

Primary Location: EMEA-Ireland-Leinster-Dublin

Employee Status: Regular

Number of Openings: 1

External Job Board Posting: Ireland - IrishJobs.ie

Company Trade Name:MSD

Scientist: Protein Purification and Characterization Job (Palo Alto, CA, US)

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Scientist: Protein Purification and Characterization-BIO004359

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We are looking for a talented protein purification and analytical biochemist to purify and carry out extensive characterization of recombinant proteins and monoclonal antibodies expressed within the Protein Sciences Department at Merck Palo Alto.

Qualifications

Education:

- Bachelors degree

Required:

- Bachelors degree with minimum of 3 years industry experience in protein purification and characterization OR Masters degree.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Biology-Discovery

Job Title:Scientist, Biology-Discovery

Primary Location: NA-US-CA-Palo Alto

Employee Status: Regular

Travel: No

Number of Openings: 1

Shift (if applicable): 1st

Hazardous Materials: Ethanol, mammalian cell culture supernatants.

Company Trade Name:Merck

Mechanisch Technician: level 3 (Oss, NB, Nederland)

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Mechanisch Technician: level 3-PRO012027

Omschrijving
Voor Lyospheres (IPT Steriles) in Oss zijn we momenteel op zoek naar kandidaten voor de functie van:

Mechanisch Technician: level 3

Over MSD
Het MSD van vandaag is wereldleider op het gebied van gezondheidszorg en werkt mee aan een gezonde wereld. Met onze geneesmiddelen, vaccins, biologische therapieën en ondersteunende diensten bieden we innovatieve behandelingen voor een betere gezondheid van mensen en dieren in meer dan 140 landen. We zijn actief betrokken bij een betere toegang tot de gezondheidszorg. Dat doen we met uitgebreid beleid, programma’s en samenwerkingsverbanden. Bij MSD in Nederland werken ongeveer 4500 medewerkers op drie verschillende hoofdlocaties Oss, Haarlem en Boxmeer.

Voor meer informatie ga naar www.werkenbijmsd.nl.

De functie
Als Technician binnen Lyospheres ben je verantwoordelijk voor het zelfstandig oplossen van multidisciplinaire storingen, het verbeteren van de apparatuur en het uitvoeren van controle- en onderhoudswerkzaamheden. Je verzorgt zelfstandig de volledige werkvoorbereiding voor het Integrated Process Team (IPT). Je beoordeelt binnengekomen werk ook voor andere technici. Je coördineert en stuurt andere technici aan vanuit je senioriteit en expertise. Je bent actief op zoek naar structurele problemen en bent in staat deze te vertalen in mogelijke oplossingen. Deze oplossingen implementeer je in samenwerking met andere technicians, operators en engineers en overige betrokkenen.

Je hebt als doel om ervoor te zorgen dat de apparatuur veilig, betrouwbaar en gekwalificeerd blijft binnen het IPT. Tevens draag je bij aan een zorgvuldig beheer van documentatie. Ook kun je met PLC besturingen werken voor het zoeken van storingen middels de PLC, het uitlezen van de diagnosebuffer, de uitgang kunnen forceren etcetera.

Kwalificaties
- Afgeronde MBO opleiding

- Gewenst is een MBO+ of HBO opleiding richting Mechatronica of Werktuigbouwkunde;

- Circa 5-7 jaar relevante werkervaring binnen een vergelijkbare functie;

- Gewenst is kennis van regelgeving binnen de farmacie ;

- VCA of bereid dit te behalen is gewenst;

- Teamplayer met zelfstartend vermogen;

- Klantgerichtheid;

- In staat om verantwoordelijkheid te nemen;

- Uitstekende communicatieve en sociale vaardigheden naar verschillende niveaus in woord als schrift.

Ploegen en tijden
We zullen met een 2 ploegenrooster van start gaan en afhankelijk van de vraag mogelijk gaan produceren in een 5*24 uur of 7*24 uur rooster.

MSD als werkgever
Keer op keer nieuwe uitdagingen aangaan, dat is wel iets wat je leuk moet vinden als je bij MSD aan de slag wilt. Want continu verbeteren is een van onze drijfveren. Dat geldt zowel voor werkprocessen als voor medewerkers. Gedrevenheid, teamwork en eigen initiatief zijn van groot belang. Bij MSD kun je je op allerlei manieren ontwikkelen. In de diepte, door je te specialiseren in je vak. Maar ook door jezelf te verbreden en door te groeien naar een leidinggevende functie. Internationaal of juist heel lokaal, er zijn talloze andere mogelijkheden om stappen te zetten in je loopbaan, te rouleren in functies of te groeien in je functie. Werken bij MSD is werken in een dynamische high tech omgeving van internationale allure, die toch sterk lokaal geworteld is in Oss, Haarlem en Boxmeer

Informatie
Voor meer informatie over deze vacature kun je contact opnemen met een van de Senior Specialists Engineering, Tonnie Göertz (0412- 665271) of Paul Mies (0412-668332).

Solliciteren
Als je interesse hebt in deze uitdagende functie kun je je interesse kenbaar maken door online je CV en een motivatiebrief te versturen.
Functie: Production / Maintenance - High NL Job Title:Mechanisch Technician: level 3

Primaire locatie: EMEA-Nederland-NB-Oss

Status werknemer
: Vast
Aantal vacatures: 1

Company Trade Name:MSD

Clinical Research Attending Veterinarian Job (DeSoto, KS, US)

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Clinical Research Attending Veterinarian-LAB000422

Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, and vaccines, as well as animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Clinical Research/Attending Veterinarian is responsible for providing veterinary oversight to the care and use of laboratory animals (primarily livestock – swine, cattle and horses and some companion research animals) at Merck Animal Health. He/She is responsible for ensuring that humane, legal, ethical, efficient, and scientifically sound research is conducted. In addition to primary care, responsibilities also include training, representation on the IACUC, and facilitating communication between Animal Services/Research Facility and Research and Development departments and Regulatory Agencies.

Qualifications

Education:

*
Doctor in Veterinary Medicine

Required Experience and Skills:

*
Individual must have a DVM specializing in livestock medicine and must be able to achieve licensure within the appropriate state.

- Good interpersonal, communication (both written and oral) and organizational skills are essential.

*
Must be able to work in a team environment.

*
Individual must be physically capable of handling, examining and treating laboratory animals of all species.

Preferred Experience and Skills:

*
Knowledge in lab animal medicine

*
Advanced graduate degrees in disease research

- Knowledge of governmental regulations, including USDA licensure and Animal Welfare Act

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives - Please read carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.


Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Laboratory Animal Vet (D.V.M.)

Job Title:Associate Director, Clinical Research

Primary Location: NA-US-KS-DeSoto

Employee Status: Regular

Travel: Yes, 10 % of the Time

Number of Openings: 1

Hazardous Materials: Animal Medicines including DEA regulated drugs

Company Trade Name:Merck
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