Senior Scientist, Stability & GMP Analytics

Pfizer; Groton (CT); On-site; USD 106,000 - 177,000; Full time

Benefits offered by this job

Health benefits

Retirement plan

Paid time off

Job summary

Pfizer is seeking a Principal Scientist in Analytical Research & Development, GMP Analytics, to lead stability strategies for drug programs and provide technical direction across interfaces. Based in Groton, CT, the role emphasizes independence, collaboration, and regulatory-compliant science.

You will design protocols, oversee data analyses, and contribute to regulatory submissions while promoting data integrity and continuous improvement.

Qualifications

• PhD with 4–8 years of relevant experience in analytical development or stability.
• MBA/MS with at least 9 years of relevant experience in pharmaceutical development.
• BA/BS with 12+ years of relevant experience in GMP environments or related fields.

Responsibilities

• Lead stability strategies for assigned drug programs and communicate across teams.
• Design stability protocols, test plans, and regulatory documentation.
• Evaluate stability results, identify risks, and partner with cross-functional experts.

Skills

Analytical development

Cross-functional collaboration

Technical writing

Regulatory documentation

Data interpretation

GMP knowledge

Quality systems

Education

PhD with 4–8 years

MBA/MS with 9+ years

BA/BS with 12+ years

Tools

Analytical software

Job description

Pfizer is seeking a Principal Scientist in Analytical Research & Development, GMP Analytics, to lead stability strategies for drug programs and provide technical direction across interfaces. Based in Groton, CT, the role emphasizes independence, collaboration, and regulatory-compliant science.

You will design protocols, oversee data analyses, and contribute to regulatory submissions while promoting data integrity and continuous improvement.