Contract Analytical Chemist — Method Dev, QC & Compliance

Pfizer; Pearl River (NY); On-site; USD 61,000 - 68,000; Full time

Benefits offered by this job

Medical, Dental, Vision

STD

LTD

Life Insurance

401(K)

Commuter Benefit Program

Job summary

Pfizer is seeking an Analytical Chemist in the New York area to perform qualitative and quantitative analyses, develop and validate methods, and ensure data integrity in a GMP/GLP environment. Responsibilities include reporting, record-keeping, and collaboration with R&D, QA/QC, and manufacturing teams.

The role requires a chemistry-related degree and 5–7 years of analytical lab experience, with emphasis on HPLC, GC, UV-Vis, FTIR, and titration.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, or a related field required; Masters or Ph.D. preferred for advanced roles.
• 5-7 years of experience in an analytical laboratory setting, preferably in pharmaceuticals, environmental science, or manufacturing.

Responsibilities

• Perform chemical analyses using techniques such as HPLC, GC, UV-Vis, FTIR, and titration
• Develop, validate, and document analytical methods for raw materials, intermediates, and finished products.
• Interpret data, prepare technical reports, and maintain accurate laboratory records.
• Ensure compliance with safety protocols, Good Laboratory Practices (GLP), and regulatory requirements (e.g., FDA, EPA)
• Troubleshoot instrumentation and analytical issues to maintain data integrity.
• Collaborate with cross-functional teams including R&D, QA/QC, and manufacturing
• Participate in laboratory audits and support continuous improvement initiatives.

Skills

Analytical instrumentation

Problem-solving

Attention to detail

Lab software

Communication skills

Team collaboration

Education

Bachelor's degree in Chemistry or Biochemistry

Master's or PhD preferred for advanced roles

Tools

MS Office

Job description

Pfizer is seeking an Analytical Chemist in the New York area to perform qualitative and quantitative analyses, develop and validate methods, and ensure data integrity in a GMP/GLP environment. Responsibilities include reporting, record-keeping, and collaboration with R&D, QA/QC, and manufacturing teams.

The role requires a chemistry-related degree and 5–7 years of analytical lab experience, with emphasis on HPLC, GC, UV-Vis, FTIR, and titration.