Offer summary
Qualifications:
Bachelor’s in Science or Engineering, Minimum 8 years pharma/biotech experience, GCP/GMP/GLP expertise and regulatory knowledge, Technical writing proficiency, Veeva experience, Supervisory experience, strong organizational skills.Key responsabilities:
- Develop/manage Supplier QA programs
- Audit GCP, GLP, GMP vendors
- Maintain quality agreements, internal procedures
- Participate in Health Authority inspections
- Review Deviations, CAPAs, Change Controls