Senior Quality Assurance Specialist - Drug Substance

Minimum Qualifications

• Bachelor's degree in a scientific, engineering or technical discipline.
• Minimum of 5 years of experience within the biopharmaceutical or pharmaceutical industry, with at least 3 years in GMP Quality Assurance.
• Experience supporting clinical and/or commercial pharmaceutical manufacturing.
• Experience with oral solid dose pharmaceutical manufacturing and packaging.
• Working knowledge of US FDA, EU EMA and ICH cGMP regulations and industry guidance.
• Experience reviewing GMP batch documentation and supporting batch disposition activities.
• Experience managing or reviewing deviations, investigations, CAPAs, change controls and other Quality System records.
• Experience supporting Contract Manufacturing Organizations (CMOs) and external manufacturing operations.
• Experience participating in GMP audits and regulatory inspections.
• Excellent written and verbal communication skills with the ability to work effectively across multiple functions and external partners.
• Strong organizational skills with the ability to manage multiple priorities while maintaining attention to detail.
• Experience authoring and reviewing SOPs and controlled GMP documentation.
• Experience using electronic Quality Management Systems (eQMS), preferably Veeva Quality, TrackWise or similar platforms.

1. 1Provide GMP Quality Assurance oversight for clinical and commercial manufacturing, and distribution activities performed at Contract Manufacturing Organizations (CMOs).
2. 2Perform Quality review of clinical and commercial batch records and supporting documentation to ensure compliance with cGMP requirements, approved manufacturing instructions and regulatory filings.
3. 3Review manufacturing, and testing documentation to support batch disposition and product release.
4. 4Review and approve deviations, investigations, CAPAs, change controls and associated Quality Management System records to ensure timely resolution and appropriate root cause analysis.
5. 5Assess quality events for potential product impact and support risk-based quality decisions.
6. 6Provide Quality support for technology transfers, process validation, engineering batches, process performance qualification (PPQ) and commercial launch activities.
7. 7Review and approve GMP documentation including Standard Operating Procedures (SOPs), Master Batch Records, specifications, protocols, reports and work instructions.
8. 8Participate as the Quality representative on cross-functional teams supporting clinical and commercial programs.
9. 9Support implementation of manufacturing, packaging and process improvements through the change management process.
10. 10Ensure compliance with Cytokinetics Quality Management System requirements, cGMP regulations and applicable global regulatory expectations.
11. 11Support qualification and ongoing Quality oversight of CMOs, contract laboratories and other GMP service providers.
12. 12Participate in internal audits, supplier audits and regulatory inspections, including inspection readiness activities and support for responses to audit observations.
13. 13Support Product Quality Reviews (PQRs), Annual Product Reviews (APRs), Quality Management Reviews and Quality Metrics reporting.
14. 14Collaborate with Regulatory Affairs, Technical Operations, Supply Chain and Manufacturing partners to support CMC submissions, post-approval changes and regulatory commitments.
15. 15Maintain GMP documentation and Quality records within the electronic Quality Management System (eQMS).
16. 16Identify opportunities to improve Quality Systems and GMP processes and participate in continuous improvement initiatives.
17. 17Provide guidance to internal stakeholders and external partners on GMP quality requirements.
18. 18Perform other Quality Assurance duties as assigned to support business objectives.