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A leading pharmaceutical company seeks a Validation Officer in Corsham. This role involves ensuring compliance with cGMP through detailed documentation and cross-departmental collaboration. The ideal candidate has two years of experience in validation and is keen to maintain quality standards. Salary ranges from £32,000 to £34,000 per annum, with additional benefits including annual leave and a pension plan.
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About Us
The Pharmaxo Group is an award winning, market leading pharmaceutical and healthcare business that serves customers, patients and medical professionals across the UK.
About Us
The Pharmaxo Group is an award winning, market leading pharmaceutical and healthcare business that serves customers, patients and medical professionals across the UK.
We Are Located In a Modern Manufacturing And Office Facility In Corsham Science Park In Wiltshire, Just 5 Miles From Chippenham And 8 Miles From Bath. The Pharmaxo Group Comprises Of
Bath ASU which produces thousands of aseptically (sterile) compounded injectable pharmaceutical products each day for hospitals and patients who are fighting cancer, living with chronic disease or in need of pain relief.
Pharmaxo Healthcare which is a growing clinical homecare provider in an expanding market offering greater convenience to patients whilst delivering efficiencies to the NHS.
Pharmaxo Scientific which develops the innovations in biotechnology, data and information technology that drive our businesses.
Your role
As Validation Officer you will deliver quality assurance services to meet cGMP requirements and the needs of the business. The role holder will be expected to provide advice on all aspects of Validation to support the quality, efficacy and safety of all products manufactured at Bath ASU.
You will be involved in the complete life cycle for commissioning of facilities, equipment, utilities, and processes, with focus on end-to-end Validation. This includes following the entire Validation Life Cycle, from the generation, execution, and review of life cycle validations documentation, developing some Key Validation Deliverables, through to assessing and mitigating Risks, planning for Validation approach and Test Strategy, Analysis, Review & Approval of Requirements and Change Management.
This position will support the Pharmaceutical Quality Management System through the creation of appropriate validation/qualification reports and presentations.
You are responsible for the generation, trending, and review of validation data; for coordinating and producing validation documentation, reports and assessing compliance requirements for equipment, computer systems and cGMP processes.
The role will involve liaising with departments including QA / QC, Production, Warehouse, IT and Maintenance as well as visits to the aseptic processing facilities.
Full job description can be found here: Validation Officer JD.pdf
Benefits
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Swindon, England, United Kingdom 1 week ago
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