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Analytical Scientist Job (Oss, NL)

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Analytical Scientist-BIO003838

Description

As an Analytical Scientist, you will be working in the department of Analytical Development and Validation. The department is responsible for late stage analytical development and commercialization of protein therapeutics within the international Merck biotech manufacturing network. Currently, the department is expanding to facilitate the market submissions of Merck’s new drugs.

Your main task is to develop and optimize analytical separation methods for the identification and characterization of protein therapeutics to support biologics development. You provide analytical support to the development of manufacturing processes and you report results in technical documents that will be used for regulatory filings. You will perform critical evaluation of analytical data against scientific standards and participate in analytical teams.

Qualifications

· Ph.D. (recently obtained) in analytical chemistry, biochemistry or equivalent with the drive to work in the laboratory;

· Demonstrated experience with method development for liquid chromatography and other separation methods combined with strong scientific problem solving skills;

· Knowledgeable of late stage method validation and statistical data evaluation;

· Ability to work independently as well as part of a multifunctional team, self-motivated, productive, customer-oriented,

· Have strong results orientation and can-do mentality;

· Have excellent interpersonal and communication skills, part of a relevant (international) network;

Information

For more information on the position please contact Joop Waterval, Principal Scientist +31(0)41266 1884

Job: Biologics, Vaccines, Analytical Formulat Job Title:Analytical Scientist

Primary Location: EMEA-Netherlands-NB-Oss

Employee Status: Regular

Number of Openings: 1

Regulatory Information Analyst Job (Prague, CZ)

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Regulatory Information Analyst-INF004126

Description

MSD is an innovative, global healthcare leader committed to improving health and well-being in 140 countries around the world. Our product categories include heart and respiratory health, diabetes, infectious diseases, consumer products and women's health. We continue to focus our research on conditions that affect millions of people around the world - diseases like Alzheimer's, Diabetes and Cancer - while further expanding our strengths in areas such as vaccines and biologics. We aspire to be the best healthcare company in the world and are dedicated to providing innovative solutions for tomorrow.

Note: MSD is known as Merck in the United States and Canada.

We are seeking energetic, forward-thinking professionals to join our Information Technology group in Prague. As part of that team, you will help launch our new IT Global Innovation Center focused on developing and applying advanced capabilities in information sciences, information security, mobility, social media and big data. You will have the opportunity to work on global teams to identify and tackle the biggest opportunities and challenges at the intersection of healthcare, information and technology. We offer project-based rotations to help with your professional development, and a flat, collaborative environment. Overall, our new Global Innovation Center in Prague offers technology professionals incredible opportunities to learn from others across the globe, to challenge themselves, and to enjoy a reward that technology careers don’t often bring: the satisfaction of helping to save lives.

Qualifications

We are seeking professionals with the following qualifications, skills and Experience:

Education: MSc Degree or BSc Degree or equivalent with relevant experience in Computer Science or Engineering or equivalent experience.

Motivated team player with excellent interpersonal skills.

Familiarity with laws, rules and regulations applicable to Pharma industry.

Strong Mathematical or Analytics experience or studies

Ability to work both independently and collaboratively.

Strong written, listening, communication skills.

The ability to advocate new ideas, even when risks are involved

Primary job responsibilities include:

Work within the Regulatory Information Management Team and with business partners to implement reporting and analytics platform to drive business decisions

Collaborate with the Global Regulatory Affairs (GRA) organization to design, develop and deliver new reports and analytics

Develop an understanding of regulatory business decisions needs and ensure platforms deliver these immediate and long term capabilities

Participate in strategic programs that will incorporate external information from regulatory agency and their interactions with other healthcare providers

We offer:

Competitive remuneration

Position in a leading global healthcare company

Challenging career

Professional growth based on performance

Innovative and flexible working environment

Wide range of benefits

*LI-LS1

Job: Information Technology Job Title:Regulatory Information Analyst

Primary Location: EMEA-Czech Republic-Prague-Prague

Employee Status: Regular

Travel: Yes, 20 % of the Time

Number of Openings: 1

ETR -- Associate Specialist Job (Whitehouse Station, NJ, US)

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ETR -- Associate Specialist:BUS000816

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.


The Information Technology group provides technology leadership and innovation for business solutions that support Merck's divisions including Research and Development (R&D), Manufacturing, Sales and Marketing, Consumer Care, Animal Health and Corporate functions such as Finance and Human Resources.

The goal of the Emerging Talent Rotational Program in the Information Technology division is to develop technical, business and leadership capabilities of top recruits through a portfolio of rotation experiences that are aligned with forward looking Merck business needs. We are looking for people passionate about technology and healthcare.

We are looking for graduates with outstanding academic records of achievement and demonstrated leadership abilities, candidates who are analytical and inquisitive about the interrelationships of various components, and perceptive, quick learners committed to helping to further Merck's vision and mission.

The program allows new hires to experience two rotations over a two year period, potentially in various business areas and sites. Each person will be partnered with a buddy, a coach, and an executive mentor who will be able to help with acculturation at Merck and career planning. Rotations are assigned based on their development interest, discussions with their mentor, and business need.

Qualifications

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.

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 ted 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.

J2W123



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


Primary Location: NA-US-NJ-Whitehouse Station

Other Locations: NA-US-NJ-Lebanon, NA-US-PA-West Point, NA-US-PA-Upper Gwynedd, NA-US-NJ-Summit, NA-US-NJ-Branchburg, NA-US-NJ-Rahway

Job Type: Full Time

Employee Status: Regular

Number of Openings: 1

Relocation Provided: Domestic (within country)

Reliability Engineering Lead Biotech Job (Oss, NL)

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Reliability Engineering Lead Biotech-FAC000334

Description

The department
The BT Facilities and Engineering team is a new centralised function that will align with the IPT Engineering teams to ensure that Reliability, utility maintenance, capital projects and Facility management operations are performed in a standardised visible manner across the site. The team will consist of 1 Facility and Engineering Lead, 1 Reliability Engineering lead, 2 Reliability Engineers, 1 CAPEX portfolio Manager, 1 Maintenance planner and 1 Facilities Engineer.

The position
As the Engineering Reliability lead you are responsible to drive the BT reliability program by developing a long term program and defining next steps for both utility and process equipment. You will work closely in collaboration with Merck Global Reliability teams.

You drive, develop and standardize the asset risk assessment policy (FMEA, HAZOPs etc?) for the site in the design of equipment and utilities. Projects could consist of purchasing new equipment, new technical improvements to insure the reliability of the equipment. Lead investigations into long term reliability problems using a data driven/six sigma approach to analyze performance, develop and implement solutions to reduce costs, improve equipment uptime and the effectiveness of asset maintenance throughout the Site.

You develop plans for, and lead the rollout of condition based monitoring and predictive maintenance techniques to the site. Serve as technical liaison for capital projects to ensure reliability, maintainability and operability of proposed new equipment. Support Operations by providing technical support on equipment and reliability issues. Support the Maintenance planning & Shutdown coordination for the business. Serve as an interface between Center of Expertise and plant (Integrated Process Team) personnel to ensure that appropriate resources are effectively focused on increasing reliability.

Qualifications

Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation

• At least 5 year’s experience in the Pharmaceutical industry or a similar operating environment which includes significant leadership roles with experience in a front-line supervisory role in operations environment.

• Knowledge of and experience in applying Six Sigma and lean methodologies and Reliability.

• Demonstrated leadership of Regulatory and corporate audits

(Compliance and Safety)

• Degree or 3rd level qualification (Engineering: Production, Mechanical, Process, Industrial, Electrical)

• Desirable evidence of Continuous Professional Development.

• Desirable for Six Sigma Green Belt.

• Desirable project management qualification such as Project Management Professional etc?

• Good knowledge of Dutch and English language (must)

*LI-LW1

Job: Facilities Management Engineering Job Title:Sr. Spclst, Engineering

Primary Location: EMEA-Netherlands-NB-Oss

Employee Status: Regular

Number of Openings: 1

Reliability Engineer Biotech Job (Oss, NL)

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Reliability Engineer Biotech-MAN002489

Description

The department
The BT Facilities and Engineering team is a new centralised function that will align with the IPT Engineering teams to ensure that Reliability, utility maintenance, capital projects and Facility management operations are performed in a standardised visible manner across the site. The team will consist of 1 Facility and Engineering Lead, 1 Reliability Engineering lead, 2 Reliability Engineers, 1 CAPEX portfolio Manager, 1 Maintenance planner and 1 Facilities Engineer.

The position
As the Reliability Engineer you are responsible to implement the BT reliability program by executing the long term program for both utility and process equipment. You will work closely in collaboration with Merck Global Reliability teams.
You implement a standardized asset risk assessment policy (FMEA, HAZOPs etc?) for the site in the design of equipment and utilities. You will be involved in projects that could consist of purchasing new equipment, new technical improvements to insure the reliability of the equipment. Lead investigations into long term reliability problems using a data driven/six sigma approach to analyze performance, develop and implement solutions to reduce costs, improve equipment uptime and the effectiveness of asset maintenance throughout the site. Assist in the development of plans and implement the rollout of condition based monitoring and predictive maintenance techniques to the site.

You serve as technical liaison for capital projects to ensure reliability, maintainability and operability of proposed new equipment. Support Operations by providing technical support on equipment and reliability issues. Support the Maintenance planning & Shutdown coordination for the business. Work with factory (Integrated Process Team- IPT) Engineering to implement the site reliability program. In addition the Reliability Engineer will ensure that the MRO process is effective to support site operations.

The Reliability Engineer will have oversight of the site Electrical infra-structure and ensure that all electrical equipment is maintained, improved, changed and modified in line with the electrical compliance guidelines (Electrisch veiligheidsvoorschrift EVV). Provide support and direction to the Centre of Expertise/IPT to manage the site electrical infrastructure and calibration programs and make contact externally for consultation where required and ensure that Electrical / calibration programs on site are compliant with all regulations.

Qualifications

• Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation

• At least 5 years’ experience in the Pharmaceutical industry or a similar operating environment.

• Knowledge of and experience in applying Six Sigma and lean methodologies and Reliability.

• Demonstrated ability to support Regulatory and corporate audits

(Compliance and Safety)

• Degree or 3rd level qualification or HBO / academic level (Engineering: Production, Mechanical, Process, Industrial, Electrical).

• Desirable evidence of Continuous Professional Development.

• Desirable for Six Sigma Green Belt.

• Desirable project management qualification such as Project Management Professional etc?

• Good knowledge of Dutch and English language (must)

*LI-LW1

Job: Manufacturing Engineering Job Title:Spclst, Engineering

Primary Location: EMEA-Netherlands-NB-Oss

Employee Status: Regular

Number of Openings: 1

Senior Specialist, Global Regulatory Affairs CMC Job (Kenilworth, NJ, US)

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Senior Specialist, Global Regulatory Affairs CMC-REG001501

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.


Position Overview

The Senior Scientist, Regulatory Affairs will supervise or lead teams in the preparation of chemical and pharmaceutical manufacturing and control (CMC) documentation for maintenance of worldwide registrations.

Additional responsibilities are as follows:

- Continual correspondence and interaction with regulatory agencies and other Merck scientists to support in-line product filings worldwide.
- Maintain working knowledge of current governmental and worldwide requirements for re-registration and post-approval changes.
- Assure that filed information on the current manufacturing and testing procedures is kept updated for each product using appropriate departmental systems.
- Ensure consistency in practices, champions best practices and promote operational excellence.
- Supervise/lead/prepare/review the chemistry, manufacturing, and controls information for worldwide marketing of pharmaceutical products (NDA, WMA) to include annual reports, registration renewals, supplements, variations and responses.
- Participate in and influences discussions regarding strategy for filing post approval changes and responding to agency or subsidiary questions.
- Track approvals of post-approval changes. Conduct follow-up.
- Participate in initiatives to promote Operational Excellence.
- Support new and existing CMC systems.
- Identify and promote best practices within CMC.
- Support filing and maintenance of pharmacopeial monographs for drug substances and drug products.
- Continually gain knowledge of current government regulations and worldwide requirements for re-registration and post-approval changes.
- Demonstrate leadership in departmental improvement activities such as system modifications, maintenance of standard operating procedures, internal guidelines, etc.
- Notify Team Lead or senior management of significant issues, where appropriate.

Qualifications

Education:

- B.S. Degree in pharmacy, biopharmaceutics, analytical chemistry, organic chemistry, chemical engineering, or a related discipline.

Preferred:

- Advanced degree

Required:

- A minimum of five years experience in chemical/pharmaceutical research or manufacturing including processing and/or analytical testing.
- Strong oral and written communication skills.
- Working knowledge of WORD, EXCEL, POWERPOINT and FirstDoc.
- Demonstrated knowledge of global regulations related to CMC.
- Developing leadership skills.
- Innovative, flexible and collaborative.
- Effective problem solving and decision making skills.
- Manage projects to achieve high productivity, prioritizes, manages effective meetings.

Preferred:

- Experience/knowledge of drug product development and maintenance and prior CMC related experience.
- Familiarity with new product registrations.

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.

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: Regulatory Affairs Generic

Job Title:Sr. Spclst, Regulatory Affairs

Primary Location: NA-US-NJ-Kenilworth

Employee Status: Regular

Travel: No

Number of Openings: 3

Shift (if applicable): 1st

Sr. Scientist Job (Kenilworth, NJ, US)

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Sr. Scientist-CHE004022

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.


We currently have an exciting opportunity to join our Analytical Sciences group located at our Kenilworth, NJ site.

In this role, you would be developing and utilizing characterization techniques to support product formulation development for new Merck products. In particular, product support includes:

• Analytical methods development and validation

• Analytical investigations

• Process and product characterization

• Developing novel analytical experiments and techniques to predict drug product performance

• Clinical study support

• Completing above tasks in an accurate and timely manner

Effective interaction with other technical, regulatory, research and manufacturing groups is critical. You'll have the opportunity to work with teams comprised of scientists and non-scientists, to effectively coordinate efforts and track the progress for multiple projects, and to provide technical leadership on interdivisional initiatives.

You would also support the implementation of new technology, including developing expertise in specialized equipment or techniques such as HPLC, LC/MS, GC/MS, Spectroscopy, and Dissolution. You would also keep abreast of innovative and novel scientific developments in the pharmaceutical industry by presenting papers at meetings, attending seminars, and reading relevant literature.

Qualifications

Education Minimum Requirements:

- PhD in Chemistry or related field

Required Experience and Skills:

- A strong academic record with a demonstrated publication record.
- Well developed verbal and written communication skills

Preferred Experience and Skills:

- Five years analytical experience strongly preferred
- PhD in Analytical Chemistry or related fields.

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.

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: Chemistry

Job Title:Sr. Scientist, Chemistry

Primary Location: NA-US-NJ-Kenilworth

Employee Status: Regular

Travel: No

Number of Openings: 1

Shift (if applicable): 1st

Hazardous Materials: standard analytical laboratory chemicals

HIV Community Liaison - (New York, NY) Job (New York City, NY, US)

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HIV Community Liaison - (New York, NY)-ACC002989

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.


The HIV Community Liaison is a key member of the HIV Sales Team in the Global Human Health Division. The incumbent plays a critical role in supporting Merck's Customer Centric Business Model.

The HIV Community Liaison will be responsible for the following:

- Engaging Allied Healthcare Providers (i.e. Case Managers, Treatment Educators, Adherence Counselors, and Social Workers) on staff in institutions serving the HIV community such as AIDS Service Organizations (ASOs), Community Based Organizations (CBOs) and / or clinics in the assigned geography.
- Supporting the training needs in these institutions by providing educational resources designed to increase patient understanding of HIV/AIDS, available treatment regimens, and optimal approaches to disease management.
- Identifying and developing national and regional advocates who can communicate objective and balanced community relevant education that is consistent with Merck's corporate objectives during medical education programs.
- Collaborating with the local field-based Merck sales team to provide information on Merck's access programs and medications that is consistent with government approved indications and brand messages to allied healthcare providers in a culturally sensitive manner.
- Communicating and demonstrating a compelling and consistent vision of Merck's commitment to HIV.
- Providing timely feedback on product/market conditions to a wide variety of internal stakeholders including marketing and public affairs.
- Ensuring all activities are within Merck policy and meet legal and compliance requirements.

Territory: This position will be based in New York City, NY and covers the five boroughs on NYC and Long Island, NY.

Qualifications

Education:

- Required: BA/BS
- Preferred: Degree in Public Health (MPH), Social Work (MSW), or Healthcare (RN, NP or other)

Required Experience:

- Minimum of (3) years experience in one of the following two areas:

- Experience working as a provider of HIV care or related services (i.e. Healthcare Professional or Medical Case Manager in an ASO, CBO, Clinic, or DoH)

OR

- Pharmaceutical Industry experience (i.e. Sales, Marketing or Community Relations) with expertise in Infectious Diseases, HIV
- Fluent in conversational and written English
- Proficient in Microsoft Office (Outlook, Word, Excel, Powerpoint)
- 10% Travel

Preferred Experience:

- Educational background in Life Sciences including Healthcare and/or Advanced Science
- Strong understanding of the HIV Therapeutic Area and the current HIV Marketplace
- Ability to understand, distill and communicate complex scientific and public health related concepts at an appropriate literacy level to diverse audiences
- Excellent interpersonal skills with ability interact with individuals from a variety of cultures, and disciplines
- Self motivated with the ability to perform with a high level of independence.
- Ability to prioritize and organize effectively
- Fluent in Spanish or other second language
- Strong presentation and training 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. 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: Account Management Generic

Job Title:Senior Specialist, Account Management

Primary Location: NA-US-NY-New York City

Employee Status: Regular

Travel: Yes, 10 % of the Time

Number of Openings: 1

Shift (if applicable): 1st

Director, Clinical Research - Oncology Job (Gwynedd, PA, US)

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Director, Clinical Research - Oncology-CLI003025

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.


The Director reports to a Senior or Executive Director in the Oncology Clinical Research Group.

Under the guidance of a supervisor, the Director has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Merck's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.

Specifically, the Director may be responsible for:

- evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications;
- developing of clinical development strategies for investigational or marketed Oncology drugs;
- planning clinical trials (design, operational plans, settings) based on these clinical development strategies;
- monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs;
- analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and
- participation in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds.

In executing these duties, the Director may:

- supervise the activities of Clinical Scientists in the execution of clinical studies;
- work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and
- assist the Senior/Executive Director in ensuring that appropriate Corporate personnel are informed of the progress of studies of Merck's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.

The Director is responsible for maintaining a strong scientific fund of knowledge by:

- maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies;
- identification of scientifically and operationally strong investigators who can assist in the development of Merck's investigational and marketed drugs;
- establishing communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of Merck drugs; and
- attend appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.

Qualifications

Education Requirement:

- M.D or M.D./Ph.D who is Board Certified or Eligible in Oncology (and Hematology)

Requred:

- Must have experience in industry or academia
- Demonstrated record of scientific scholarship and achievement;
- A proven track record in clinical medicine and background in biomedical research is essential
- Prior specific experience in clinical research and prior publication is desirable but not necessary
- Strong interpersonal skills, as well as the ability to function in a team environment are essential.

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.

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: Clinical Research (M.D.)

Job Title:Prin. Scientist, Clinical Research

Primary Location: NA-US-PA-Upper Gwynedd

Other Locations: NA-US-NJ-Kenilworth

Employee Status: Regular

Travel: Yes, 25 % of the Time

Number of Openings: 2

IVRS Coordinator Job (Rahway, NJ, US)

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IVRS Coordinator-CLI003133

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.


Responsible for the development and implementation of IVRS (Interactive Voice Response System) systems in collaboration with IVRS Vendor team. Responsible for creating and enforcing IVRS standards, managing vendor performance, supporting system change requests, and supporting training & education for stakeholders. Ensures vendors are planning and managing timelines, and employing risk management techniques. Provides input regarding IVRS development processes. May lead or support process improvement activities. May mentor new and junior staff. Interacts with both technical and clinical staff to ensure their needs are met.

Qualifications

Education Requirement:

* Bachelor's Degree

Required:

* 2+ years experience in IVRS, Clinical Supplies, Clinical Research, or Database design & development

Preferred:

* 2+ years experience supporting development & implementation of IVR systems in support of clinical trials

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: Clinical Data Management

Job Title:Spclst, Clinical Data Mgmt

Primary Location: NA-US-NJ-Rahway

Other Locations: NA-US-PA-West Point

Employee Status: Regular

Travel: No

Number of Openings: 1

Associate Director Regulatory Affairs CMC - Merck Animal Health Job (Summit, NJ, US)

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Associate Director Regulatory Affairs CMC - Merck Animal Health-REG001483

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.


The Regulatory Affairs CMC Associate Director position at Merck manages activities for US and International Animal Health pharmaceutical products. This is a new position and reports into the Director, Regulatory Affairs. This position supports world wide regulatory functions and sits at the Summit, New Jersey site.

This position is responsible for the follow areas:

- Provide regulatory expertise for the global pharma product portfolio on the CMC part of the regulatory dossiers (e.g. assess CMC changes and provide regulatory requirements/guidance)
- Prepare and submit regulatory filings
- Represent CMC regulatory affairs on cross functional teams and development projects.
- Act as a primary FDA Liaison for the Animal Health division

through the following
DUTIES:

1. Independently prepare CMC dossiers, expert reports, answers to questions, and other documentation to support new product registrations in the US, EU, and international markets.
2. Independently prepare supplements, variations, and answer questions for approved products including site transfers, process/analytical changes, and other regulatory CMC submissions for US, EU and other international markets to assure regulatory compliance.
3. Develop, communicate, and implement strategies for the earliest possible regulatory approvals.
4. Proactively participate on project teams Critically review all data and documents to ensure regulatory requirements are met. Collaborate in the development of studies to fulfill regulatory quality requirements.
5. Serve as a primary FDA liaison for the division for CMC related topics. Coordinate phone calls, meetings, and other correspondence with the agency and trade association as appropriate.
6. Develop and maintain strong knowledge of the national registration requirements for animal health products in the major animal health markets, i.e. European Union, United States, Japan, EU-like countries (Canada, Australia) and the BRIC countries (Brazil, Russia, India, China). Actively follow the development and emergence of new regulatory requirements and assess their impact on the existing pharmaceutical product range and development projects.
7. Critically review and approve change authorizations. Determine the regulatory filing strategy. Ensure that adequate information is provided to support the submission and filing strategies. Prepare and submit the filing.
8. Develop and train regulatory personnel.

To learn more about Merck Animal Health - visit http://www.merck-animal-health.com/

Qualifications

Required Qualifications:

* Minimum of a B.S. in Pharmacy, Chemistry or Science.

* A minimum of five (5) years of Regulatory CMC experience

* A minimum of ten (10) years of pharmaceutical experience

* US and International Regulatory CMC experience

Preferred Education:

* An advanced degree in a Science, Engineering or Regulatory field

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.

*LI-CG1


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


Job: Regulatory Affairs Generic

Job Title:Assoc. Dir, Regulatory Affairs

Primary Location: NA-US-NJ-Summit

Employee Status: Regular

Number of Openings: 1

2014 PPDM Intern - Bioanalytics Job (West Point, PA, US)

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2014 PPDM Intern - Bioanalytics:ADM006035

Description

Merck is a global healthcare leader with a diversified portfolio of prescription medicines, vaccines, biologic therapies, and consumer care 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 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.


MRL Intern- Pharmacokinetics, Pharmacodynamics and Drug Metabolism (PPDM) – Bioanalytics.

The Future Talent Program features internships that last 9-12 weeks and will include one or more projects. These opportunities in our Merck Research Labs (MRL) can provide you with great development and a chance to see if we are the right company for your long-term goals. The projects that you work in can be in one of the following areas:

The Bioanalytics Groups at Merck provide quantitative analysis of biologically derived samples for all Merck discovery and development programs. The main technology used in these groups is liquid chromatography and mass spectrometry (LC-MS). The groups are well equipped with the most modern LC-MS equipment available. Projects in Bioanalytics will involve development and application of new approaches for drug analysis using mass spectrometry. Specific intern projects will be developed with the mentor consistent with completion in the timeframe of the internship. Coaching and training will be provided on new skills and approaches as needed.

Qualifications

Education:

- Enrolled in a BS/BA, MS or PhD degree (program) in Chemistry, Biochemistry, Pharmaceutical Sciences,

or related areas, with preference to analytical chemistry

Required:

- Strongly recommended is experience in quantitative analysis, liquid chromatography, and mass spectrometry.
- Strong interpersonal skills

- Proficient oral and written communications skills

- Desire to work in a collaborative team environment

- Ability to adapt to new technologies, business (situations)

- Ability to adapt to a rapidly changing work environment

- Ability to solve problems by creative application of new and existing technology, processes and information.
- Must be available for a period of 9-12 weeks, beginning June 2014.

Preferred:

- G.P.A of 3.0 or higher

- Knowledge of sample preparation technologies for small molecules, proteins and peptides is desirable.

- Eligible to work in U.S. on a full-time basis

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.



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


Primary Location: NA-US-PA-West Point

Job Type: Intern

Employee Status: Regular

Number of Openings: 1

Sr. Scientist, Chemistry Job (Rahway, NJ, US)

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Sr. Scientist, Chemistry-CHE004023

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.


The Analytical Chemistry department of Merck Research Laboratories has a Senior Scientist position available to be located in the Rahway, New Jersey research facility. The Senior Scientist is a laboratory-based scientific role in a fast-paced, multidisciplinary team environment. The role is tasked with solving high complexity analytical problems related to development of active pharmaceutical ingredients (APIs). The successful candidate must have demonstrated successful application of state-of-the-art analytical techniques to solve chemistry problems, including chiral / achiral separations (HPLC / SFC/ GC / CE / IC), MS, NMR, and other spectroscopy techniques (UV-vis / IR / Fluorescence / Raman). Experience in bio-conjugate purification and characterization is a plus. Applicants must have effective organizational, multi-tasking, oral / written communications skills, and strong scientific leadership.

Qualifications

Educational Requirement:

- PhD degree in analytical chemistry or a closely-related field with clear evidence of strong past academic achievement.

Required:

- HPLC/UHPLC, LC-MS, spectroscopy
- Ion exchange chromatography, size exclusion chromatography,

Preferred:

- Bio-molecule purification and charachterization, hydrophobic interaction chromatography, CE, automation for analysis, and new analytical technology evaluation and development

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.

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: Chemistry

Job Title:Sr. Scientist, Chemistry

Primary Location: NA-US-NJ-Rahway

Employee Status: Regular

Travel: No

Number of Openings: 1

Hazardous Materials: Chemicals

Process/Construction Engineer Biotech Job (Oss, NL)

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Process/Construction Engineer Biotech-PRO010946

Description

The department

The manufacturing team Down Stream Processing Biotech (DSP) is with approximately 100 employees responsible for the purification of commercial products and materials for clinical studies. These purifications are done in our modern state of the art facilities under Good Manufacturing Practices (GMP) rules. In the beginning of 2012 a new, large scale production part of the factory has been taken in use in which Merck's new Monoclonal Antibodies will be purified. To meet the strong growth of these products, a second expansion of the facility is currently in design. The team consists of 7 Process/Construction Engineer s and 2 Maintenance Engineers.

The position

As Process/Construction Engineer Biotech you are responsible for the design of equipment and utilities, you will act as project lead regarding, budget, scope and timelines. Projects could consist of purchasing new equipment, new technical improvements to insure the reliability of the equipment. For this you use your Sigma knowledge.

Furthermore you are responsible for the startup and maintaining qualification status of complex automated process equipment, installations and utilities of the Factory, such as purified water (PW), water for injection (WFI) and Caustic-Acid.

You write problem solving proposals for manufacturing related processes in order to improve performance (compliance, financial, robustness) of assets. You train and instruct Manufacturing personnel by the execution of asset support related activities, develop standardized work in cooperation with improvement lead and operations lead.

You asses asset related deviations applying problem solving tools and Root Cause analysis and take necessary actions to follow-up on deviations

You are responsible that data, protocols and documentation is up-to-date, to comply with stringent regulations. In GMP and EHS audits you act as a SME (Subject Matter Expert).

Qualifications

· HBO/academic level (Process/construction engineering is a preference)

· At least 5 years of relevant experience in (bio)chemical manufacturing under GMP (must)

· Good knowledge of Dutch and English language (must)

· Project management experience (must)

· Willingness to certify for or in possession of Green Belt

· Passion for Lean and continuous improvement

· Knowledge of IT systems, such as PLC is preferred

· Available for 32 to 40 hours a week

· Comply with GMP and EHS requirements

Information

For more information on the position please contact Desiree Janssen, Maintenance & Reliability Lead BT, +31 (0)412 66 13 05 or 06-13043643

Job: Production / Maintenance Job Title:Process/Construction Engineer Biotech

Primary Location: EMEA-Netherlands-NB-Oss

Employee Status: Regular

Number of Openings: 1

Resource Management Specialist Job (Prague, CZ)

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Resource Management Specialist-INF004215

Description

MSD is an innovative, global healthcare leader committed to improving health and well-being in 140 countries around the world. Our product categories include heart and respiratory health, diabetes, infectious diseases, consumer products and women's health. We continue to focus our research on conditions that affect millions of people around the world - diseases like Alzheimer's, Diabetes and Cancer - while further expanding our strengths in areas such as vaccines and biologics. We aspire to be the best healthcare company in the world and are dedicated to providing innovative solutions for tomorrow.

Note: MSD is known as Merck in the United States and Canada.

We are seeking energetic, forward-thinking professionals to join our Information Technology group in Prague. As part of that team, you will help launch our new IT Global Innovation Center focused on developing and applying advanced capabilities in information sciences, information security, mobility, social media and big data. You will have the opportunity to work on global teams to identify and tackle the biggest opportunities and challenges at the intersection of healthcare, information and technology. We offer project-based rotations to help with your professional development, and a flat, collaborative environment. Overall, our new Global Innovation Center in Prague offers technology professionals incredible opportunities to learn from others across the globe, to challenge themselves, and to enjoy a reward that technology careers don’t often bring: the satisfaction of helping to save lives.

Qualifications

We are seeking professionals with the following qualifications, skills and Experience: Education Minimum Requirement:
Bachelor level degree in Computer Sciences, Information Systems, Business Administration or equivalent.
Required Experience and Skills:
3-4 years of project support, scheduling and resource leveling experience.
Knowledge of Resource Planning processes.
Ability to analyze and process data from various sources and validate it to ensure data consistency.
Creative thinking and drive for leveraging insights to ensure continuous process improvement.
Flexibility to adapt to changing requests and timescales as well as to work under tight deadlines.
Ability to work both within local as well as within virtual, geographically dispersed teams.
Ability to work independently and with others with minimal supervision.
High level of persuasive and negotiation skills.
Strong skills in Microsoft Office (Excel, Word, Outlook, PowerPoint, Access, Project).
Desired Experience and Skills:
Consulting background is an advantage.
Qualifications in the field of Project Management (PMI PMP, Prince2, CAPM).

Primary job responsibilities include:
Resource Planning and Scheduling
Provide support to Resource & Capacity Planning Manager.
Work closely with the central IT Project Portfolio Management team to help drive the implementation and execution of resource management practices in the Global Innovation Centre.
Develop, implement and maintain Resource Planning processes and procedures, whilst continuously striving to improve them.
Be local expert for scheduling, resource allocation and team sizing. Assess project needs and open roles, find adequate candidates and ensure resource utilization.
Represent the Resource Planning team in projects and provide input regarding what impact any new or existing developments/initiatives have on the team’s ability to achieve service level and the deployment of resources.
Demand Supply Balancing
Drive forward the Operational Demand Supply Plan recommending targets for new financial year based on historical trends and forthcoming initiatives.
Maintain Supply plan for the Recruitment throughout the year, highlighting any variances against plan and offering potential solutions.
Ensure frequent, open communication between Resource Planning and Central Project Portfolio management team in order to utilize feedback and understand service delivery trends.
Predict changes and development of the Project portfolio based on inputs from Platform Leads.
Make recommendations for the recruitment of new roles based on platforms development needs and current team capacity constraints.
Metrics and analysis
Perform hands-on data manipulation, analysis, and reporting for executives.
Create and maintain a labor model.
Update, process and report data using in MS Excel.

We offer:
Competitive remuneration
Position in a leading global healthcare company
Challenging career
Professional growth based on performance
Innovative and flexible working environment
Wide range of benefits

*LI-BP1

Job: Information Technology Job Title:Resource Management Specialist

Primary Location: EMEA-Czech Republic-Prague-Prague

Employee Status: Regular

Travel: Yes, 20 % of the Time

Number of Openings: 1

Sr. Scientist Job (Kenilworth, NJ, US)

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Sr. Scientist-CHE004022

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.


We currently have an exciting opportunity to join our Analytical Sciences group located at our Kenilworth, NJ site.

In this role, you would be developing and utilizing characterization techniques to support product formulation development for new Merck products. In particular, product support includes:

• Analytical methods development and validation

• Analytical investigations

• Process and product characterization

• Developing novel analytical experiments and techniques to predict drug product performance

• Clinical study support

• Completing above tasks in an accurate and timely manner

Effective interaction with other technical, regulatory, research and manufacturing groups is critical. You'll have the opportunity to work with teams comprised of scientists and non-scientists, to effectively coordinate efforts and track the progress for multiple projects, and to provide technical leadership on interdivisional initiatives.

You would also support the implementation of new technology, including developing expertise in specialized equipment or techniques such as HPLC, LC/MS, GC/MS, Spectroscopy, and Dissolution. You would also keep abreast of innovative and novel scientific developments in the pharmaceutical industry by presenting papers at meetings, attending seminars, and reading relevant literature.

Qualifications

Education Minimum Requirements:

- PhD in Chemistry or related field

Required Experience and Skills:

- A strong academic record with a demonstrated publication record.
- Well developed verbal and written communication skills

Preferred Experience and Skills:

- Five years analytical experience strongly preferred
- PhD in Analytical Chemistry or related fields.

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.

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: Chemistry

Job Title:Sr. Scientist, Chemistry

Primary Location: NA-US-NJ-Kenilworth

Employee Status: Regular

Travel: No

Number of Openings: 1

Shift (if applicable): 1st

Hazardous Materials: standard analytical laboratory chemicals

Sr. Scientist, Engineering Job (Kenilworth, NJ, US)

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0
Sr. Scientist, Engineering-PRO011366

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.


Qualifications

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: Process Engineering

Job Title:Sr. Scientist, Engineering

Primary Location: NA-US-NJ-Kenilworth

Employee Status: Regular

Travel: No

Number of Openings: 1

Shift (if applicable): 1st

Hazardous Materials: No

Associate Director, Outcomes Research Job (Whitehouse Station, NJ, US)

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Associate Director, Outcomes Research-OUT000230

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.


Qualifications

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: Outcomes Research -Health Econ

Job Title:Associate Director, Outcome Research

Primary Location: NA-US-NJ-Whitehouse Station

Employee Status: Regular

Travel: Yes, 10 % of the Time

Number of Openings: 1

Shift (if applicable): 1st

Senior Financial Analyst Order-to-Cash Job (Haarlem, NL)

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Senior Financial Analyst Order-to-Cash-SHA000196

Description

For our Global Finance Services (GFS) organization located in Haarlem we are currently recruiting a:

Senior Financial Analyst Order-to-Cash (OtC)

This role will be responsible for supporting both domestic and export markets in GFS OtC related transactions.

About MSD

MSD is working to help the world be well. Through our medicines, vaccines, biologic therapies, and animal health products, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. MSD has a workforce of almost 4500 in the Netherlands at three main sites. MSD is also known as Merck & Co., Inc. in the US and Canada.For more information, visit our website: www.werkenbijmsd.nl

The position

Reporting into the Director General Accounting the Senior Financial Analyst will be responsible for supervising a small team and reviewing and approving SBS OtC financial transactions for the markets. He/ she will review allowances, discounts and other compensation proposed by the markets and will support new business deals, advice and review new contracts and coordinate new customer account requests.

As part of the role the Senior Financial Analyst Order- to -Cash (OTC) will be responsible for:

· Serving as one point of contact for the markets in case of OtC related issues;

· Providing sales reports to the markets in support of daily operations and audit;

· Coordinating GFS OTC month-end activities including sales recognition analysis according to US GAAP & sales reporting input;

· Coordinating compliance & audit for GFS OtC;

· Actively monitoring, reviewing and implementing new SAP functionalities;

· Actively participating in projects locally and regionally.

Qualifications

· Bachelor’s degree in Business Economics, Finance or Accountancy;

· At least five years of experience in Finance, preferably and /or detailed process knowledge in at least one of the sub areas of Order to Cash;

· Experience with SAP system & advanced MS Office;

· Continuous Improvement mindset and strong business analysis skills;

· Ability to work cohesively as part of a team;

· Ability to work with a range of customers on multiple tasks;

· Ability to work diplomatically and effectively with a wide range of people from different business functional areas and different countries;

· Ability to make effective decisions and work independently;

· Strong influencing and communication skills and ability to manage key stakeholders effectively;

· Excellent interpersonal skills, pro-active, flexible and stress resilient;

· Excellent verbal and written communication skills in English, Dutch is a plus.

A good place to work

MSD is an attractive employer offering interesting opportunities in Research & Development, production and staff departments for an enormous range of disciplines such as biologists, chemists, process engineers, technicians, mechatronic engineers, pharmacists and operators. MSD always seeks ‘best-in-class’ employees at all levels. We expect a lot from our people and MSD has a lot to offer them as well. Team spirit, entrepreneurship, integrity, leadership and cross-border communication skills are what MSD values and rewards most. If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Information

For more information about the role, please contact Hans Verhagen, Director General Accounting, via e-mail: hans_verhagen@merck.com or by phone: +31(0)23-5153256.

Application

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

Acquisition by recruitment agencies is not appreciated.

*LI-RS1

Job: Shared Services Job Title:Sr. Spclst, Shared Svcs Finance

Primary Location: EMEA-Netherlands-NH-Haarlem

Employee Status: Regular

Number of Openings: 1

Product Manager, Afrin / Coricidin Job (Summit, NJ, US)

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Product Manager, Afrin / Coricidin-PRO011393

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.


The Product Manager (PM) for Afrin/Coricidin is the general manager of these two (2) brands and interacts with every part of the organization that touches these businesses. The PM identifies key issues and opportunities, strategies and tactics, and the investment needed to impact the short and long term growth of the brands. This is a people leadership role with one direct report.

Responsibilities include and are not limited to the following:

- Product and Brand Knowledge: Be an expert on the brands and the categories and draw on that knowledge to make recommendations to further the businesses. Find ways to maximize our claims to tap into consumer insights and address competitive pressures. Leverage strong knowledge of brands and category to educate cross functional team members so they can finds ways to add value. Leverage knowledge to develop effective marketing plans.
- Facilitating External Market Analysis: Lead gathering of data inputs to answer key strategic questions about category dynamics and brand performance. Guide direct report and cross functional team members in analysis of market trends, sales, shipments, inventory flow, forecasts, etc. Provide input and direction to Market Research Department for the development and execution of all consumer market research. Analyze Market Research data to uncover new consumer insights, find ways to leverage those insights and disseminate learning and action plan to cross functional team.
- Strategic Thinking and Planning: Lead marketing plan process including establishing key issues, objective strategies and tactics. Develop multi year growth strategies and provide input on innovation vision.
- Marketing Communications: Lead development of all marketing communication with outside agencies to develop effective advertising, PR, consumer and professional promotion and packaging. Recommend marketing communication strategies for the brand. Oversee development of creative briefs to ensure creative work is on strategy. Lead development of annual media plans and adjust when appropriate.
- Financials: Manage brand P&L’s and oversee management of marketing budgets. Examine ROI of all projects and benchmark against best practices, similar brands and or programs.
- Facilitating Customer Relationships: Lead annual communication of brand plans to sales, align brand objectives and strategies with customer objectives, be the key interface with field sales.
- New Product Management: leverage product and brand knowledge and consumer insights to identify product improvements and cost savings opportunities, develop and champion new product business cases, lead cross functional teams to develop marketing support to achieve new product objectives, oversee development of sales materials. Provide input to Global Franchise group on the certain new product initiatives being handled by that team.
- Project Management: oversee and challenge project teams to ensure the execution of product plans that enhance brand value and deliver brand objectives and strategies. Manage advertising and other promotional/PR agencies, working with more senior levels, to ensure the development of appropriate strategies and tactics to achieve band objectives.

The Project Manager must be able to exhibit these behaviors:

- High degree of comfort making rapid decisions with uncertain or incomplete information
- Excellent project management and planning skills to execute a high volume of projects on time and with excellence
- Ability to set priorities and adjust given changes in market conditions or internal resources, etc
- Build effective work teams by positively influencing and working well with cross functional team members as well as mentoring/coaching/developing a direct report
- Excellent communication and presentation skills (both oral and written)

Qualifications

Education:

* Required: BA/BS

* Preferred: MBA/MS

- Preferred: Emphasis in Marketing

Required Experience:

* Minimum of (3) years Consumer Brand Management experience

* 15% Travel

Preferred Experience:

- Experience working on Consumer OTC Products

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.

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


Job: Product Management/Marketing

Job Title:Senior Specialist, Marketing

Primary Location: NA-US-NJ-Summit

Employee Status: Regular

Travel: Yes, 15 % of the Time

Number of Openings: 1

Shift (if applicable): 1st
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