QA Operations - Drug Product, QA Manager
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Overview
Job Description
What You'll Do
Manage quality oversight at Drug Product Contract Manufacturing Organizations (CMOs). Act as QA operations lead with assigned CMOs, including review of manufacturing batch records and batch release certificates. Ensure CMO SOPs and Master Batch Records are in compliance with cGMPs and serve as technical review for deviations, change records, protocols, and CAPAs generated from or pertaining to Calcilytix or other BridgeBio affiliates, as needed.
Responsibilities
- Represent QA Operations on internal and external project teams, audits and inspections, and participate in monitoring of CMO performance
- Review and manage master and executed manufacturing batch records from CMOs, including release activities, and related documents such as specifications, analytical and microbiological methods, stability study/protocols, process and method validation protocols and reports
- Author and perform quality review of SOPs and quality events (deviations/investigations, OOSs/OOTs, change controls, supplier notifications, etc.)
- Lead Disposition of Drug Product
- Communicate/escalate manufacturing deficiencies/non-conformances to management, present issues during escalation, and work with CMOs to ensure timely resolution
- Support review of regulatory filings
- Support audit of CMOs
Where You'll Work
This role requires in-office collaboration 2-3x per week in our San Francisco office.
Who You Are
- Bachelor's Degree in a science discipline with 8+ years of experience within a biopharmaceutical company, or contract research organization
- Strong knowledge of GMP, SOPs, Quality Systems (e.g. Lot Release, Deviation, Change Control, CAPA,) ICH and GxP principles
- Strong knowledge of FDA and other clinical trial regulations
- Prior experience in QC, Analytical Development and process validation highly desired
- Excellent verbal and written communication skills, with strong customer focus
- Excellent organizational skills, ability to manage multiple tasks and competing priorities, and maintain meticulous attention to detail
- Travel up to 10% total time
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Submit 10x as many applications with less effort than one manual application.
