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Sr. Scientist, Analytical R&D

MSD

Sr. Scientist, Analytical R&D

full-timePosted: Jan 29, 2026

Job Description

Categories: Pharmaceutical, Research, Analytical Chemistry, Drug Development

Job Description

The Small Molecule Analytical Research and Development group has an opening for a Senior Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

In your role as Senior Scientist, you will be part of a team developing innovative analytical methodologies for early to late phase programs with application to drug substance and a broad array of drug product dosage forms, combination products and modalities through analytical characterization, imaging tools, and data analy­sis. You would also contribute towards regulatory submissions to enable clinical trials.

Your main responsibilities include:

  • Driving solutions to analytical development challenges for synthetic small molecule, peptide and oligonucleotide active pharmaceutical ingredients and pharmaceutical products using conventional and novel technologies

  • Designing scientific studies to inform the selection and deep understanding of synthetic routes, formulation compositions, and manufacturing processes.

  • Implementing analytical methods for laboratory development, as well as release and shelf-life assessment of clinical supplies under good manufacturing practice (GMP) conditions.

  • Providing leadership not only on drug development pipeline projects, but also innovative technology teams shaping analytical methods and tools of the future.

  • Authoring regulatory submission documents across the project development lifecycle, as well as responding to agency questions.

  • Documenting work in a detailed and timely manner.

  • Collaborating effectively with internal and external partners.

  • Presenting results of experiments and innovation efforts to project teams and at various cross-functional forums.

  • Engaging in the external scientific community, e.g. through participation in professional organizations, conferences, and publications.

  • Travel Requirement: 5% Travel

Education Minimum Requirements:

Applicants must hold one of the following:

  • PhD in Chemistry, Pharmaceutical Science, or related discipline

  • Master’s Degree in Chemistry, Pharmaceutical Sciences, or related discipline plus at least 3 years of pharmaceutical industry experience.

  • Bachelor’s degree in chemistry, Pharmaceutical Sciences or related discipline, plus at least 7 years of industry experience.

Required Experience and Skills

  • A proven record of strong technical problem solving and innovative research experience, supported by scientific publications.

  • Excellent written and oral communication skills.

  • Strong leadership, collaboration and interpersonal skills.

Preferred Experience and Skills

While not required, experience in one or more of the following areas is preferred:

  • Experience with large molecule characterization (oligonucleotides, enzymes, peptides, etc.)

  • Chromatography (e.g. LC, GC) method development, analysis and troubleshooting.

  • Other advanced analytical techniques such as mass spectrometry or dissolution.

  • Data science

#AR&D

Required Skills:

Accountability, Adaptability, Analytical Method Development, Assay Development, Bioanalytical Analysis, Biochemical Assays, Cell-Based Assays, Chromatographic Techniques, Communication, GMP Environments, Innovative Thinking, Nuclear Magnetic Resonance (NMR) Analysis, Process Analytical Technology (PAT), Strategic Thinking, Team Management, Technical Writing, Ultra Performance Liquid Chromatography (UPLC)

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement​

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$117,000.00 - $184,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits.  Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

02/6/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Locations

  • Rahway, New Jersey, United States

Salary

Estimated Salary Rangemedium confidence

126,000 - 176,000 USD / yearly

Source: AI Estimation

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Analytical Method Developmentadvanced
  • GMP Complianceadvanced
  • Regulatory Submissionsadvanced
  • Data Analysisintermediate
  • Scientific Study Designadvanced
  • Imaging Tools and Characterizationintermediate

Required Qualifications

  • Experience in analytical development for small molecules, peptides, or oligonucleotides (experience)
  • Background in drug substance and drug product dosage forms (experience)
  • Proficiency in conventional and novel analytical technologies (experience)
  • Leadership in drug development projects and innovation teams (experience)

Responsibilities

  • Drive solutions to analytical development challenges for synthetic small molecule, peptide, and oligonucleotide APIs and pharmaceutical products using conventional and novel technologies
  • Design scientific studies to inform selection and understanding of synthetic routes, formulation compositions, and manufacturing processes
  • Implement analytical methods for laboratory development, release, and shelf-life assessment of clinical supplies under GMP conditions
  • Provide leadership on drug development pipeline projects and innovative technology teams shaping future analytical methods and tools
  • Author regulatory submission documents across the project lifecycle and respond to agency questions
  • Document work in a detailed and timely manner while collaborating with internal and external partners and presenting results

Benefits

  • Culture: Strong ethics, integrity, and passion for improving human health through innovative science
  • Career: Opportunity to collaborate with talented global colleagues and expand career in a leading pharmaceutical company
  • Professional: Experience exceptional science, innovative drug delivery technologies, and predictive analytical tools
  • Work Environment: Join a dedicated team in Rahway, NJ, contributing to early to late phase programs

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MSD logo

Sr. Scientist, Analytical R&D

MSD

Sr. Scientist, Analytical R&D

full-timePosted: Jan 29, 2026

Job Description

Categories: Pharmaceutical, Research, Analytical Chemistry, Drug Development

Job Description

The Small Molecule Analytical Research and Development group has an opening for a Senior Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

In your role as Senior Scientist, you will be part of a team developing innovative analytical methodologies for early to late phase programs with application to drug substance and a broad array of drug product dosage forms, combination products and modalities through analytical characterization, imaging tools, and data analy­sis. You would also contribute towards regulatory submissions to enable clinical trials.

Your main responsibilities include:

  • Driving solutions to analytical development challenges for synthetic small molecule, peptide and oligonucleotide active pharmaceutical ingredients and pharmaceutical products using conventional and novel technologies

  • Designing scientific studies to inform the selection and deep understanding of synthetic routes, formulation compositions, and manufacturing processes.

  • Implementing analytical methods for laboratory development, as well as release and shelf-life assessment of clinical supplies under good manufacturing practice (GMP) conditions.

  • Providing leadership not only on drug development pipeline projects, but also innovative technology teams shaping analytical methods and tools of the future.

  • Authoring regulatory submission documents across the project development lifecycle, as well as responding to agency questions.

  • Documenting work in a detailed and timely manner.

  • Collaborating effectively with internal and external partners.

  • Presenting results of experiments and innovation efforts to project teams and at various cross-functional forums.

  • Engaging in the external scientific community, e.g. through participation in professional organizations, conferences, and publications.

  • Travel Requirement: 5% Travel

Education Minimum Requirements:

Applicants must hold one of the following:

  • PhD in Chemistry, Pharmaceutical Science, or related discipline

  • Master’s Degree in Chemistry, Pharmaceutical Sciences, or related discipline plus at least 3 years of pharmaceutical industry experience.

  • Bachelor’s degree in chemistry, Pharmaceutical Sciences or related discipline, plus at least 7 years of industry experience.

Required Experience and Skills

  • A proven record of strong technical problem solving and innovative research experience, supported by scientific publications.

  • Excellent written and oral communication skills.

  • Strong leadership, collaboration and interpersonal skills.

Preferred Experience and Skills

While not required, experience in one or more of the following areas is preferred:

  • Experience with large molecule characterization (oligonucleotides, enzymes, peptides, etc.)

  • Chromatography (e.g. LC, GC) method development, analysis and troubleshooting.

  • Other advanced analytical techniques such as mass spectrometry or dissolution.

  • Data science

#AR&D

Required Skills:

Accountability, Adaptability, Analytical Method Development, Assay Development, Bioanalytical Analysis, Biochemical Assays, Cell-Based Assays, Chromatographic Techniques, Communication, GMP Environments, Innovative Thinking, Nuclear Magnetic Resonance (NMR) Analysis, Process Analytical Technology (PAT), Strategic Thinking, Team Management, Technical Writing, Ultra Performance Liquid Chromatography (UPLC)

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement​

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$117,000.00 - $184,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits.  Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

02/6/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Locations

  • Rahway, New Jersey, United States

Salary

Estimated Salary Rangemedium confidence

126,000 - 176,000 USD / yearly

Source: AI Estimation

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Analytical Method Developmentadvanced
  • GMP Complianceadvanced
  • Regulatory Submissionsadvanced
  • Data Analysisintermediate
  • Scientific Study Designadvanced
  • Imaging Tools and Characterizationintermediate

Required Qualifications

  • Experience in analytical development for small molecules, peptides, or oligonucleotides (experience)
  • Background in drug substance and drug product dosage forms (experience)
  • Proficiency in conventional and novel analytical technologies (experience)
  • Leadership in drug development projects and innovation teams (experience)

Responsibilities

  • Drive solutions to analytical development challenges for synthetic small molecule, peptide, and oligonucleotide APIs and pharmaceutical products using conventional and novel technologies
  • Design scientific studies to inform selection and understanding of synthetic routes, formulation compositions, and manufacturing processes
  • Implement analytical methods for laboratory development, release, and shelf-life assessment of clinical supplies under GMP conditions
  • Provide leadership on drug development pipeline projects and innovative technology teams shaping future analytical methods and tools
  • Author regulatory submission documents across the project lifecycle and respond to agency questions
  • Document work in a detailed and timely manner while collaborating with internal and external partners and presenting results

Benefits

  • Culture: Strong ethics, integrity, and passion for improving human health through innovative science
  • Career: Opportunity to collaborate with talented global colleagues and expand career in a leading pharmaceutical company
  • Professional: Experience exceptional science, innovative drug delivery technologies, and predictive analytical tools
  • Work Environment: Join a dedicated team in Rahway, NJ, contributing to early to late phase programs

Target Your Resume for "Sr. Scientist, Analytical R&D" , MSD

Get personalized recommendations to optimize your resume specifically for Sr. Scientist, Analytical R&D. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Sr. Scientist, Analytical R&D" , MSD

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

MSDMerckPharmaPharmaceuticalResearchAnalytical ChemistryDrug Development

Answer 10 quick questions to check your fit for Sr. Scientist, Analytical R&D @ MSD.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.