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Senior Quality Control Inspector, Bridgend
Client: PCI Pharma Services
Location: Bridgend, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Reference: a250a2f0b8b7
Job Views: 5
Posted: 02.06.2025
Expiry Date: 17.07.2025
Job Description:
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Responsibilities:
* Supervise the QC Inspectors to meet operational requirements and company objectives.
* Organise the QC Inspectors to ensure core QC processes are operating in line with EU GMP standards and defined company KPIs, including incoming inspection, master label proofs, label inspection, in-process checks, finished product inspection, retails process, and material review board.
* Plan and schedule the QC Inspectors' workload to meet operational schedules and ensure deadlines are met.
* Identify and implement efficiencies and improvements for QC Inspector processes to ensure the QC department delivers expected internal and external customer service.
* Ensure Non-Conformance Reports and QC-related deviations/CAPA’s are identified, completed, and closed within defined timescales.
* Identify, initiate, and oversee QC change controls.
* Organise performance assessments and training of QC Inspectors as per company policies and procedures.
* Formulate and maintain QC Inspectors' objectives, ensuring alignment with PCI and site business plans and objectives.
* Ensure all activities are carried out in accordance with GMP.
* Support special projects, site priorities, and new project introductions for QC as required.
* Support audits within the QC area.
* Provide cross-functional support with the Senior Despatch QC and QC inspector roles.
* Assist QA with investigations of customer complaints and deviations.
Additional responsibilities include:
* Preparing monthly reports for the QC systems.
* Managing MRB reports.
* Scheduling QC inspectors and staff rotas.
* Developing training and development plans for QC staff.
Join us and be part of building the bridge between life-changing therapies and patients.
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