QC Analyst - Potency

Job Title: QC Analyst - Potency Location: Rockville, MD Type: Contract Schedule: Monday - Friday 8am-5pm

Overview Biopharmaceutical Company is seeking a QC Analyst to join their team in Rockville, MD!

Responsibilities

• Perform testing and analysis of potency samples in accordance with established protocols and Good Manufacturing Practices (GMP).
• Ensure accurate documentation of test results and maintain thorough records for compliance and audit purposes.
• Operate laboratory instrumentation such as HPLC, spectrophotometers, and other analytical tools to assess sample quality.
• Interpret data, prepare reports, and communicate findings to cross-functional teams.
• Maintain a clean, organized, and compliant lab environment, adhering to safety standards and company policies.
• Collaborate with quality assurance and manufacturing teams to support product release and stability studies.

• Bachelor’s degree in Chemistry, Biology, Biochemistry, or a related scientific field.
• 4-5 years of experience in GMP environment performing ELISA's, MSD, and bioassays for potency residuals within a biotech company.
• Experience with good documentation practices required. (may consider CLIA or GLP experience if candidates do not have GMP)