QC Associate Scientist

About the role

We’re hiring an Associate Scientist with analytical experience to join a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO partners and generic drugs. This is a great opportunity to work with an industry leader that focuses on their expertise and competence in all of the companies processes!

Responsibilities

• Perform routine HPLC and GC analysis to support API method transfers, including data generation, interpretation, and documentation in compliance with GMP standards
• May perform other analytical testing (e.g., FTIR, KF, NMR)
• Support GMP method transfers, including protocol/report preparation
• Conduct release testing for raw materials, intermediates, and APIs
• Investigate out-of-specification (OOS) results and document findings
• Ensure timely and compliant data generation to meet project timelines
• Review analytical data for accuracy and GDP compliance

Qualifications

• Bachelor’s degree in chemistry or related field
• Minimum of 3 years’ hands-on experience performing HPLC and GC analysis within GMP pharmaceutical manufacturing
• Demonstrated experience in analytical method transfers
• Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory documentation practices

Benefits

• PTO
• Health/vision/dental insurance
• HSA
• 401(k) with match
• Holiday pay

Schedule

M-F 8a-5p

Pay

Pay Rate Low: 75000 | Pay Rate High: 90000