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Sunny

Quality Assurance Officer - Project

Id Job: 31727a4

🏢 On-site
💼 Sunny
📍 Bangor Teifi, Wales
🕒 1 day ago
💰 37000 – 60000 GBP ANNUAL

Job Description

  • Located in a beautiful part of Wales
  • Willing to travel within UK, EU and internationally for up to 15% of time
  • Excellent salary incl private healthcare etc.

Project QA Officer | Ceredigion - West Wales
Permanent
Bio-Pharmaceutical industry

KEY DUTIES…
  • Accountable for QA oversight of the external manufacturing operations to ensure the corresponding GMP compliance in every phase according to regulatory expectations.
  • Provide guidance and supporting external manufacturing with Product Disposition;
  • cGMP Document Review – including reviewing both master and executed Batch Manufacturing Records, validation/qualification protocols and reports
  • Coordination/support for batch release
  • Arranging, attending, taking minutes from calls with CMOs/CTLs
  • Review and approve External Investigations and ensure issues are tracked within company QMS system
  • Ensure escalation of substantial issues to the Quality Assurance Lead;
  • Preparing and executing the external auditing program.
  • Ensuring that GXP rules are obeyed adequately to the project stage.
  • Preparation and review of Quality Agreements.
  • Review, analysis and approval the change controls, product release test results, , lab investigation reports, and manage OOS investigation etc.



WHAT YOU WILL NEED…
  • Science degree including - Biology, Microbiology, Biochemistry, Pharmacy, Chemistry or Biotechnology (or equivalent) is preferred.
  • Experience dealing directly with both regulatory agency personnel as well as the CDMO provider representatives is preferred.
  • Experience in operational GMP in a pharmaceutical manufacturing environment including batch disposition is desirable.
  • An experience in Quality or Quality Assurance functions within the Pharmaceutical or Medical Device Industry is required is preferred.
  • Understanding of the regulatory/Quality responsibilities active pharmaceutical ingredient (DS) and drug product (DP) batch disposition.
  • Demonstrated negotiation and influencing skills.
  • Knowledge of MS Word, Excel, PowerPoint and data management platforms.
  • Willing to travel within UK, EU and internationally for up to 15% of time
  • Strong written, verbal and presentation skills.



BENEFITS…
  • Join a friendly, supportive team
  • Company bonus scheme
  • Private healthcare
  • Excellent Pension & holiday allowance

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