Senior Quality Control Analyst

Role: Senior QC Analyst responsible for establishing and managing QC laboratory operations and testing programs for raw materials in biopharma manufacturing. Primary objectives include ensuring raw material quality and compliance to GMP standards. Responsibilities: set up and stock QC labs, perform routine and non-routine testing (e.g., pH, ELISA, spectroscopy), manage sample shipments to external labs, establish identity testing methods, review data, write SOPs and protocols, participate in equipment validation, and support audits. Qualifications: BA/BS in Chemistry/Biochemistry or related science; 3-5 years GMP laboratory experience with strong analytical skills; familiarity with industry testing requirements for raw materials. Preferred: experience with biological raw materials, GMP environment, and water testing. High-value details: role supports biopharma manufacturing, likely related to immunotherapy or oncolytic platforms, with a focus on raw material testing and GMP compliance. Location: Framingham MA, onsite 5 days/week.