Cpl Life Sciences

Quality Officer

Leamington Spa
17 Feb 2021
18 Mar 2021
Nawa Kamona
Quality, QA / QC
Full Time
Contract Type
Experience Level
Experienced (non-manager)

CPL is recruiting for a Quality Officer to join the QA team of our client at their new site for an 18-month contract. This position, which covers a broad range of responsibilities, would be a great fit for a candidate with 1-2 Quality experience within a pharmaceutical/biotech environment, who is looking to develop a career in QA. You will be responsible for general maintenance of the Quality Management System (QMS) and supporting the QA Manager in maintaining compliance standards.

Key Responsibilities:
Support continuous improvements in the Quality Management System (QMS) and maintain compliance of Quality processes
Work with the managers and their teams to maintain all aspects of the QMS e.g. Change Controls, Non-Conformities, CAPAs, Customer Complaint
Provide support as required for notified bodies and client audits, as well as performing internal audits according to schedule
Perform desk-based and on-site audits of subcontractors and suppliers
Working with other QA staff, provide support to Operations team, e.g. report review and QA statements, as well as assisting in training of personnel on matters relating to the QMS.
Maintain thorough knowledge and understanding ISO 15189 requirements, Regulatory expectations and guidance documents as these pertain to the work performed at the site

Required Experience:
Significant experience of operating within ISO Quality Management Systems of operational laboratory environments and working to relevant ISO accreditation standards; ISO 15189, ISO 17025, ISO 9001.
A team player, with good analytical reasoning, customer focus, communication and change orientation in a fast-paced environment.
Experience liaising with stakeholders regarding quality and compliance
Experience conducting audits and hosting external auditors
Desired Experience
Experience with Ideagen Qpulse Quality Management System

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