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
Numbers & Facts
Location
San Francisco - 1800 Owens, CA
Skills
Analysis Skillsunmatched
Analytical Developmentunmatched
CMOSunmatched
Change Controlunmatched
Clinical Practices/Protocolsunmatched
Communication Skillsunmatched
Contract Manufacturingunmatched
Contract Research Organization (CRO)unmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Customer Relationsunmatched
Detail Orientedunmatched
Drug Productsunmatched
FDA (Food and Drug Administration)unmatched
GMP (Good Manufacturing Practices)unmatched
GxPunmatched
ICH Regulationsunmatched
Manufacturingunmatched
Microbiologyunmatched
Multitaskingunmatched
Organizational Skillsunmatched
Performance Analysisunmatched
Presentation/Verbal Skillsunmatched
Process Validationunmatched
Quality Assuranceunmatched
Quality Controlunmatched
Quality Managementunmatched
Regulatory Submissionsunmatched
Standard Operating Procedures (SOP)unmatched
Time Managementunmatched
Validation Planunmatched
Willing to Travelunmatched
Writing Skillsunmatched
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