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MSD

Senior Scientist, Chemistry

MSD

Senior Scientist advancing analytical chemistry for Merck’s global pharmaceutical manufacturing network. Developing methods, troubleshooting laboratory workflows, and supporting compliant drug-substance supply.

Posted 8/7/2026full-timeRahway • New Jersey, Pennsylvania • 🇺🇸 United StatesSenior💰 $117,000 - $184,200 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in analytical techniques, including chromatography and spectroscopy, with a strong foundation in synthetic organic chemistry and API development. Proven ability to lead cross-functional teams, ensure compliance with cGMP standards, and effectively communicate technical information.

Highest-signal resume keywords
Analytical TechniquesChromatographySpectroscopyCGMP KnowledgeData Integrity

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Analytical ProceduresValidation ProtocolsTechnical ReportsExperimental DesignsRegulatory Submission DocumentsProblem-SolvingRisk-Management PlansAPI DevelopmentDrug Substance DevelopmentProduct Specifications
Soft Skills
Strong Verbal CommunicationStrong Written CommunicationInterpersonal SkillsCultural SensitivitySelf-Motivated
Industry Keywords
Pharmaceutical DevelopmentContract Manufacturing OrganizationsContract Research OrganizationsCross-Functional TeamsWorld Class Supplier

About the role

Key responsibilities & impact
  • Author analytical procedures, development and validation protocols and reports, technical reports, experimental designs, and regulatory submission documents
  • Perform investigations and technical troubleshooting
  • Provide documentation and technical input during regulatory and internal inspections and audits
  • Apply working knowledge of data integrity
  • Train staff on analytical techniques and problem solving as needed
  • Influence external sites in the worldwide manufacturing network to identify, implement, and troubleshoot laboratory test methods, workflows, and materials
  • Support compliant, robust, and responsive supply
  • Drive lead-time reduction and efficiency gains supporting World Class Supplier and Operationalizing Quality goals

Requirements

What you’ll need
  • MS in Chemistry or related discipline with at least 5 years of relevant pharmaceutical development experience, or PhD in Analytical Chemistry or related discipline
  • Working knowledge of analytical techniques used in commercial testing of raw materials, intermediates, and drug substances
  • Strong verbal and written communication skills
  • Flexibility to work in a dynamic environment with internal and external communications
  • Strong interpersonal skills and cultural sensitivity
  • Self-motivated ownership and accountability for issues through completion
  • Ability to adapt quickly to changes and develop risk-management plans
  • Willingness to travel abroad
  • Knowledge of developing analytical techniques such as chromatography and spectroscopy and product specifications for drug substance development and registration
  • Fundamental knowledge of synthetic organic chemistry
  • Working knowledge of API development and commercialization
  • Experience with contract manufacturing organizations and/or contract research organizations
  • Experience working in cross-functional teams
  • Strong technical background, problem-solving skills, leadership abilities, cGMP knowledge, and data integrity knowledge

Benefits

Comp & perks
  • Annual bonus
  • Long-term incentive, if applicable
  • Medical, dental, and vision healthcare
  • Other insurance benefits for employee and family
  • Retirement benefits, including 401(k)
  • Paid holidays
  • Vacation
  • Compassionate days
  • Sick days
  • Visa sponsorship
  • Relocation: Domestic