Site Compliance Manager 3587-1

Site Compliance Manager 3587-1
  • Competitive
  • Temporary
  • Halewood, Merseyside, England, UK Halewood Merseyside UK L24 9GR
Job Ref: J2162224
Sector: Science
Sub-sector: Pharmaceuticals
Date Added: 07 October 2021
Site Compliance Manager - liverpool

Job Title: Site Compliance ManagerLocation: Speke, LiverpoolRate: £19.18 per hourWorking Pattern: Monday - Friday (3 days on site, 2 days remotely)Contract: 12-18 monthsAre you experienced working in a pharmaceutical manufacturingenvironment? SRG are working with a global pharmaceutical company that are worldleaders in vaccine production. You will be joining a small compliance team tosupport with GMP guidelines, implement process improvements company wideand occasionally liaise with the global teams in California and Australia.Key Responsibilities:* You will support on Quality systems to ensure compliance with company standards and GMP regulatory guidelines* Develops, maintains and improves GMP-related quality control systems including standard operating procedures (SOPs)* Supports quality systems related to Validation, LIMS, Calibration, Document Management, Deviation Management, CAPA, Change Control, complaints, and Enterprise Learning Management* Writes and manages validation plans, ensuring appropriate, timely validation/revalidation is maintained* Conducts internal audits and assists with 3rd party quality audit; plans and implements continuous improvement projects* Collaborates to resolve technical issues, provide quality training and communicate best practices* Support and execute site quality and compliance improvements, working closely with relevant stakeholders on site. * Manage and execute process new draft guidelines and regulations and develop implementation plans as required.Requirements:* Bachelor's degree in relevant scientific discipline (Chemistry, Biology, Microbiology, etc.) * 5+ years' quality systems experience in pharmaceutical manufacturing/cGMP regulated environment* Knowledge of cGMP, FDA and EMA requirements* Confident using trackwise or equivalent software* Experienced in deviation writing and change controlsIf this role is of interest to you, (or you know anyone who might be suitable), please click the link to apply or email your CV to Tom O'Neill at and a time that is convenient for me to call you.

06/11/2021 10:53:58
GBP 0.00 0.00 Annum
Contact Consultant:
Tom O'Neill

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