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QA Specialist
QA Specialist
wirral,merseyside
Dec 21, 2024
  • Hours Full Time
  • Salary 1.00 - 20.00 GBP Hourly
  • Recruiter CK GROUP
  • Closes 11 Jan 2024
  • Course No
  • Contract type Permanent
  • Recruiter Type Direct Employer
Description

CK Group are recruiting for a Associate Scientist to join a global pharmaceutical company, based in the Wirral on a contract basis for 12 months. This role offers hybrid working.Salary:Up to GBP20.00ph PAYECompany:Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.Location:Wirral. This site provides services across multiple areas to the client's offices in Europe and beyond. There is a high-performing, talented and multicultural team of over 350 employees working in Finance, Customer Service, IT, HR, Tax and more.QA Specialist Role: Reviews clients and label vendor specifications in accordance with relevant regulatory requirementsReview and approve vendor generated label proofs/specifications and other related documentsPerforms specific quality related functions such as Quality/GMP training, materials/products releasing, validation, quality incident investigations to ensure compliance with GMP regulations and clients standardsSupports in the investigation of non-conformances and quality incidentsReviews and approves documents related to Quality Systems such as validation protocols/reports, change control, or Procedural Documents to support the release function.Support internal and/or external audits as required.Participates in assigned training including GMP and safety training Your Background: Degree or equivalent in pharmacy, engineering, or life sciencesRelevant experience in the pharmaceutical industry or related healthcare environmentLabelling experience in the pharmaceutical industry is highly desiredAbility to plan, manage and execute multiple projectsAbility to understand and apply regulatory and CGMP principlesGood knowledge of rigorous pharmaceutical and/or scientific documentation practices and change control processes (e.g., revision control) is preferred Apply:It is essential that applicants hold entitlement to work in the UK. Please quote job reference 56406 in all correspondence.

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