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quality assurance veeva capa cgmp biologics📋 Description
- Perform QA activities to ensure compliance with Revance procedures and regulatory requirements.
- Review SOPs, batch records, labeling, test methods, protocols, and reports.
- Review production batch records, deviations, investigations, and disposition.
- Review and approve quality records in a timely manner.
- Act as compliance resource; guide deviations, investigations, CAPAs, changes.
- Perform area approvals and product inspections; support raw materials and reserve samples.
🎯 Requirements
- Bachelor’s degree in relevant field
- 6+ years' experience in quality assurance/biologics or related field
- Good working knowledge of cGMP standards for commercial biologics
- Prior experience with regulatory inspections and Veeva is desired
- Specific vision abilities include passing a visual acuity test
- Excellent interpersonal, verbal, and written communication skills
🎁 Benefits
- Competitive compensation including base salary and annual performance bonus
- Generous healthcare, HSA and 401k matching, life and disability
- Paid time off, holidays, and parental leave
- Pet insurance and wellness discounts
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