- Coordinate the implementation of the company's quality management system relevant to GCP, including external vendor oversight and training on quality procedures.
- Act as the main point of contact for Immunomonitoring and R&D labs, providing support and back-up to the Senior Clinical Quality Assurance Manager.
- Assist in the planning and conduct of audits, including internal, vendors, clinical sites, external laboratories, suppliers.
- Minimum of 4+ years of experience in a GCP QA role within the pharmaceutical/biotechnology industry, with experience providing quality support to Clinical laboratories.
- Expert knowledge of pharmaceutical regulations, standards, and current industry regulatory practices related to GCP and GCLP.
- Bachelor's Degree in Life Sciences, Pharmacy, or Regulatory.
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QA Specialist, Pharmaceutical - City of London, Greater London, United Kingdom - Proclinical Staffing
Description
Senior Clinical Quality Assurance Specialist | Permanent | Biotechnology | London Proclinical are searching for a dedicated professional for a Senior Clinical QA Specialist to ensure and establish best practices in our clients organisation.
Responsibilities:
Requirements:
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
