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MSD Quality Assurance Specialist 
United Kingdom, England, London 
54941429

28.07.2024

Job Description

Primary activities include:
  • Completes batch reviews to ensure compliance to SOPs, GMPs and applicable regulations.
  • Review and approve production and analytical documentation accompanying the release of drug substance, drug product and packaged finished goods to ensure conformance to appropriate SOPs, GMP and regulatory requirements, including supporting QP certification.
  • Actively communicate and collaborate with functional areas to develop a strong working relationship and understanding of roles and responsibilities. Utilise this network to help resolve comments and issues that arise during audit and review.
  • Follows standard procedures and consults with manager/supervisor to ensure resolution of exceptions.
  • Compiles data for reports and presentations, provides data interpretation draws conclusions.
  • Carries out all assignments to the standards of compliance, efficiency, innovation, accuracy and safety in accordance with Company and regulatory requirements.
  • Keeps abreast of cGMP requirements as described in applicable worldwide regulations.
  • AnyAdditional activities as assigned by the manager/supervisor

Current Contingent Workers apply


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


08/01/2024


A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.