Company

CK Group- Science, Clinical and TechnicalSee more

addressAddressMoreton, Merseyside
type Form of workContract
salary Salary£0 - £20/hour
CategoryIT

Job 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 £20.00ph PAYE
Company:
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 requirements
  • Review and approve vendor generated label proofs/specifications and other related documents
  • Performs specific quality related functions such as Quality/GMP training, materials/products releasing, validation, quality incident investigations to ensure compliance with GMP regulations and clients standards
  • Supports in the investigation of non-conformances and quality incidents
  • Reviews 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 sciences
  • Relevant experience in the pharmaceutical industry or related healthcare environment
  • Labelling experience in the pharmaceutical industry is highly desired
  • Ability to plan, manage and execute multiple projects
  • Ability to understand and apply regulatory and CGMP principles
  • Good 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.
Refer code: 2475080. CK Group- Science, Clinical and Technical - The previous day - 2024-01-10 14:42

CK Group- Science, Clinical and Technical

Moreton, Merseyside
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