QA Supervisor ensuring product quality and compliance for biopharma clients. Overseeing QA operations, evaluating deviations, and managing investigations with a focus on regulatory standards.
Responsibilities
Work with other departments to ensure the quality of products and compliance to internal procedures and external standards
Provide quality oversight for client facing QA operations, including Batch Record review and final product lot disposition
Evaluate events, deviation incidences and determine whether to escalate to an investigation
Conduct Change Control assessments and quality review
Approve investigations and create/monitor associated CAPAs
Establish relationships with internal and external customers to address quality matters
Review, develop, and improve quality system procedures
Lead improvement projects and communicate status to management
Manage assigned QA staff, providing feedback and development
Assist with internal audits and supplier audits as needed
Interface with clients on documentation and compliance concerns
Requirements
Bachelor’s Degree in a relevant scientific discipline preferred
Minimum of 5+ years of pharmaceutical or biotech industry experience
Experience performing RCA, technical writing, and working with quality related investigations
Knowledge of laboratory and production equipment and IQ/OQ/PQ
Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820)
Some experience working with international regulations such as ICH.
Experience using Risk Management Tools (FMEA, HACCP, PHA, etc.)
Familiarity with ICH Q9
Knowledge of electronic systems including SAP, LIMS, MasterControl, Trackwise, Veeva, or electronic batch recording systems
Microsoft Office suite knowledge and proficiency with Excel is desirable.
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