About the Role
Part-time (60-80%) Senior QA Auditor to lead QA activities across clinical research (GCP) and manufacturing (GMP), ensuring compliance with SOPs and regulations and managing the Quality Management System (QMS).
Key Responsibilities
- Manage QMS, SOPs, change control, deviations and CAPAs.
- Conduct internal and external audits and oversee third-party auditors and vendor qualification.
- Review batch records, investigate OOS results and perform root cause analysis.
- Coordinate with Regulatory Affairs for submissions and inspections (MHRA, FDA, EMA).
Requirements
- At least 7 years’ experience in pharma/biotech/CRO with Clinical Operations and QA exposure.
- Bachelor’s degree in a life science or related field.
- Deep knowledge of ICH-GCP and GMP regulations.
- Strong analytical, communication and stakeholder management skills.
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