Quality Control Scientist – Stability & cGMP Compliance

Planet Pharma; Concord (OH); On-site; USD 65,000 - 90,000; Full time

Job summary

Planet Pharma is seeking an Associate Quality Control Scientist to join a cGMP-regulated pharmaceutical lab in Ohio. You will perform analytical testing on materials, in-process samples, finished products, and stability samples, and contribute to data reviews and regulatory compliance.

The role requires a chemistry degree and experience in a QC lab, with proficiency in standard instrumentation and collaboration with QA, manufacturing, and clients to support batch release and stability studies.

Qualifications

• Bachelor's degree in Chemistry or a related scientific discipline required.
• Minimum of 3 years of related pharmaceutical analytical laboratory experience with a B.S. degree, or 1 year with an M.S. degree, or an equivalent combination of education and experience.
• Relevant experience in a Quality Control laboratory is required.
• Experience working in a cGMP and/or GLP-regulated environment is required.

Responsibilities

• Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using techniques such as HPLC, GC, KF, FTIR, XRD, DSC, TGA, PSD, NMR, ICP-MS, ICP-OES, and other laboratory instrumentation as required.
• Support stability programs through sample management, stability chamber monitoring, testing, and generation of stability data.
• Coordinate timely and compliant generation of analytical data to support client projects and manufacturing operations.
• Review laboratory data for technical accuracy, completeness, compliance, and adherence to good documentation practices.
• Conduct OOS, OOT, and laboratory investigations and support implementation of corrective and preventive actions (CAPAs).
• Author and review protocols, reports, specifications, analytical methods, and related laboratory documentation.

Job description

Planet Pharma is seeking an Associate Quality Control Scientist to join a cGMP-regulated pharmaceutical lab in Ohio. You will perform analytical testing on materials, in-process samples, finished products, and stability samples, and contribute to data reviews and regulatory compliance.

The role requires a chemistry degree and experience in a QC lab, with proficiency in standard instrumentation and collaboration with QA, manufacturing, and clients to support batch release and stability studies.