GCP Quality Specialist

Posted 08 September 2023
Salary Competitive Package
Job type Permanent
Discipline Quality
Contact NameDixie Rowley

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:
  • 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.
You will be responsible for:
  • 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.
You will bring the following:
  • Background working within the pharmaceutical quality assurance space.
  • Strong understanding and knowledge of GCP regulations.
  • Experience working within early phase clinical trials / radiopharmaceutical products.
Please reach out to find out more!
  • Mobile: 03333076496
  • Email: dixie.rowley@biotalent.com