PHARMAFull-time
Senior Associate Scientist Chem - Analytical (R)
GROTON (US)ONSITEPOSTED: 8/17/2026
PHARMAFull-time
HIRING ORGANIZATIONPFIZERBiopharmaceutical / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Role Overview
Senior Associate Scientist Chem - Analytical (R) is a Senior Associate Scientist / PAT Specialist role within Pfizer Research & Development. The position is part of the cross-functional Pfizer Continuous Manufacturing Module (PCMM) team and provides technical expertise for Process Analytical Technology (PAT) instrumentation in a clinical solid oral dose GMP manufacturing environment. The role combines hands-on analytical instrument management, manufacturing campaign support, analytical data analysis, method/process development, documentation, troubleshooting, and collaboration across multidisciplinary teams.
Core Responsibilities
Manage and maintain PAT analytical instrumentation used during manufacturing campaigns, including Near-Infrared (NIR) and Focused Beam Reflectance Measurement (FBRM) instruments and Advanced Process Control (APC) software.
Prepare, install, calibrate, and perform performance checks on PAT instrumentation.
Monitor analytical instrumentation output during manufacturing campaigns using advanced process-control software, real-time dashboards, and analytics.
Provide analytical support to clinical solid oral dose GMP manufacturing campaigns.
Contribute to development and continuous improvement of drug-product manufacturing processes.
Author and maintain System Life Cycle (SLC) documentation, Standard Operating Procedures (SOPs), technical reports, and other technical documentation.
Present analytical data to project teams and participate in critical review of analytical results.
Prepare clear, accurate, and submission-ready technical reports and supporting documentation.
Work effectively with project team members across multiple functions and disciplines.
Demonstrate proficiency with a wide variety of software and information systems used in analytical and manufacturing environments.
Troubleshoot analytical instruments and resolve technical problems affecting manufacturing activities.
Meet project milestones under general supervision and manage expectations for assigned projects.
Support delivery of technology, technology-transfer activities, data, and documentation suitable for project milestones and submissions.
Follow safe laboratory practices and applicable GMP requirements.
Technical & Analytical Expertise
Process Analytical Technology (PAT).
Near-Infrared (NIR) instrumentation.
Focused Beam Reflectance Measurement (FBRM) instrumentation.
Advanced Process Control (APC) software.
Real-time manufacturing data monitoring and analytics.
Analytical data interpretation and review.
Instrument calibration and performance verification.
Instrument troubleshooting and problem solving.
Analytical chemistry principles.
Clinical solid oral dose manufacturing.
GMP-regulated manufacturing environments.
System Life Cycle (SLC) documentation.
Standard Operating Procedures (SOPs).
Technical report preparation.
Technology transfer and submission-ready documentation.
Minimum Qualifications
Bachelor's degree in Analytical Chemistry or a related field.
Minimum 3 years of relevant experience in a laboratory or manufacturing environment, academic research laboratory, or industrial research laboratory.
Ability to deliver project milestones under general supervision.
Ability to manage project expectations and deliver technology, data, and documents required for technology transfer or submission activities.
Strong problem-solving and instrument-troubleshooting capability.
Ability to follow safe laboratory practices.
Excellent oral and written communication skills.
Strong attention to detail and organizational skills.
Ability to multitask and meet project timelines.
Team-oriented approach and effective interpersonal skills.
Preferred Qualifications
Pharmaceutical industry experience.
Experience working in a regulated environment.
Experience with PAT instrumentation such as NIR and FBRM.
Experience with APC software.
Experience performing data analysis in a GMP environment.
Team & Working Environment
Member of the cross-functional Pfizer Continuous Manufacturing Module (PCMM) team.
Fast-paced, multidisciplinary research and manufacturing environment.
Requires effective interaction with peers, project teams, and leaders.
Work location assignment is On Premise in Groton, Connecticut.
Relocation support may be available depending on business needs and candidate eligibility.
Compensation & Benefits
Annual base salary range: $68,600 to $114,300.
Eligible for Pfizer's Global Performance Plan with a target bonus of 7.5% of base salary.
Benefits include a 401(k) plan with Pfizer matching contributions and an additional Pfizer Retirement Savings Contribution.
Paid vacation, holidays, and personal days.
Paid caregiver/parental and medical leave.
Medical, prescription drug, dental, and vision coverage.
Compensation and benefits are aligned with the location of hire.
Employment Eligibility
Candidates must be authorized to work in the United States by any employer.
U.S. work visa sponsorship, including TN, O-1, and H-1B sponsorship, is not available for this role now or in the future.
The position requires permanent U.S. work authorization.
Pfizer is an E-Verify employer.
Relocation assistance may be available based on business needs and eligibility.
Equal Opportunity & Accessibility
Pfizer is committed to equal employment opportunity and nondiscrimination in employment and recruitment.
Pfizer provides accessibility support for candidates who need assistance with the website, application process, or interviewing.
The supplied posting also references Pfizer's candidate guidelines regarding acceptable and prohibited uses of AI during recruitment.
REQUIRED VERIFIED SKILLS
Analytical Chemistry
Process Analytical Technology
PAT Instrumentation
NIR
FBRM
APC Software
Instrument Calibration
Instrument Performance Checks
Instrument Troubleshooting
Analytical Data Analysis
GMP
Clinical Solid Oral Dose Manufacturing
Laboratory Practices
System Life Cycle Documentation
SOPs
Technical Reporting
Technology Transfer
Data Review
Project Milestones
COMPENSATION & REWARDS
USD 0.7L - 1.1L per annum
ORGANIZATION CONTEXT & CULTURE
Pfizer Inc. is an American multinational pharmaceutical and biotechnology corporation. It is dedicated to the discovery, development, manufacturing, marketing, and sale of medicines and vaccines worldwide. The company focuses on breakthrough science to deliver innovative treatments across various therapeutic areas to improve health outcomes.
TEAM SIZE: 80,000+ employees
INDUSTRY: Biopharmaceutical / Healthcare
RECOMMENDED TRAINING
1/5
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