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GCP Quality Specialist
Job description
GCP Quality Specialist – New Haven (Connecticut) – Competitive Package
I am currently working with an established and global pharmaceutical company that are looking to recruit a Quality Specialist to sit within the GCP function and take charge of quality related responsibilities and duties.
This opportunity will offer you:
I am currently working with an established and global pharmaceutical company that are looking to recruit a Quality Specialist to sit within the GCP function and take charge of quality related responsibilities and duties.
This opportunity will offer you:
- The opportunity to upskill and develop your QA GCP experience, learning from the best in the business and reporting into a Senior Director.
- The chance to work for an established and global organisation with a strong reputation within the industry.
- Ensuring GCP regulations are adhered to on site.
- Reviewing and approving of procedures and process across the organisation’s facility.
- Supporting and being involved in internal audits and regulatory inspections.
- Background working within the pharmaceutical quality assurance space.
- Strong understanding and knowledge of GCP regulations.
- Experience working within early phase clinical trials / radiopharmaceutical products.
- Mobile: 03333076496
- Email: dixie.rowley@biotalent.com