Senior Analytical Scientist - Chemistry, GMP R&D

Pfizer Inc; Groton (CT); On-site; USD 69,000 - 114,000; Full time

Benefits offered by this job

401(k) matching

Retirement savings contribution

Paid vacation

Job summary

Pfizer Inc. in Groton, CT is seeking a Senior Associate Scientist in Analytical Research & Development to support drug release and stability testing using chromatography, spectroscopy, and dissolution methods.

You will work with GMP notebooks and engage with QA/CMC to ensure timely data submission and release of clinical supplies. The role requires a BS with 2+ years or an MBA/MS and offers exposure to a range of analytical techniques, software systems, and a collaborative team in a fast-paced

Qualifications

• BA/BS with at least 2 years of experience or MBA/MS with any years of experience.
• Experience in problem solving and instrument troubleshooting.
• Demonstrated oral and written communication skills, especially adherence to laboratory GMP notebook practices.
• Experience with software and information systems (ELN, OneLab, CisPro, Empower, LIMS).
• Ability to work in a GMP laboratory environment and in a team setting.

Responsibilities

• Perform lab work supporting analytical testing of pharmaceutical projects.
• Run analytical methods, test materials, and release drug substances and drug products to support clinical release or extensions.
• Interact with project teams, QA and regulatory CMC to support investigations and release of clinical supplies.
• Demonstrate proficiency with a wide variety of software and information systems.
• Collaborate with peers and leaders in a fast-paced, multi-disciplinary environment.

Skills

Analytical testing

Chromatography

KF

Spectroscopy

Dissolution

Data analysis

GMP notebook

Education

BS in Chemistry/Related

MBA/MS preferred

Tools

OneLab

CisPro

Empower

LIMS

Job description

Pfizer Inc. in Groton, CT is seeking a Senior Associate Scientist in Analytical Research & Development to support drug release and stability testing using chromatography, spectroscopy, and dissolution methods.

You will work with GMP notebooks and engage with QA/CMC to ensure timely data submission and release of clinical supplies. The role requires a BS with 2+ years or an MBA/MS and offers exposure to a range of analytical techniques, software systems, and a collaborative team in a fast-paced