Analytical Scientist - Drug Substance Development

Pfizer; Groton (CT); On-site; USD 79,000 - 132,000; Full time

Job summary

Pfizer in the United States is seeking a Scientist to develop analytical strategies for drug substances and products across development phases, including method validation, impurity control, and transfers. You will collaborate with cross-functional teams and mentor peers to solve analytical challenges.

Apply chromatography, dissolution, IR/ Raman, MS, and NMR techniques to support projects, forecast resources, write technical reports, and assist with global regulatory submissions.

Qualifications

• MS in Analytical Chemistry or related field with 4–6 years of experience (or BS with 6–8 years).
• Experience leading multi-disciplinary teams and meeting timelines.
• Ability to learn new techniques and solve analytical problems.
• Strong oral and written communication, data visualization, and reporting.

Responsibilities

• Develop analytical strategies for drug substances and products across development phases.
• Transfer analytical methods and design stability studies for shelf life assignments.
• Collaborate with colleagues and mentor peers to solve technical challenges.
• Prepare technical reports and contribute to regulatory submissions.

Skills

Analytical Chemistry

Project leadership

Data analysis

Communication skills

Attention to detail

Chromatography

Mass spectrometry

NMR

IR/Raman spectroscopy

Dissolution

Particle size analysis

Education

MS in Analytical Chemistry or related field

BS in a related field

Tools

LIMS

Chromatographic Software

Veeva

Electronic notebooks

Job description

Pfizer in the United States is seeking a Scientist to develop analytical strategies for drug substances and products across development phases, including method validation, impurity control, and transfers. You will collaborate with cross-functional teams and mentor peers to solve analytical challenges.

Apply chromatography, dissolution, IR/ Raman, MS, and NMR techniques to support projects, forecast resources, write technical reports, and assist with global regulatory submissions.