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Salary:
34.94 per hour PAYE
Quality Qualified Person role:
- To ensure the principles and guidelines of cGMP have been met during manufacturing, packaging and testing operations.
- To verify all batch related documentation is compliant with the requirements of the regulatory authorities.
- To review and certify batches in line with business shipment schedules.
- To ensure Product Licences (Marketing Authorisations), ANDAs, Manufacturer's Licence, Technical Agreements, CE Certification requirements have been met to ensure compliance.
- To ensure planned changes or deviations are supported by appropriate sampling, inspection, testing and check to ensure compliance with the requirements of the regulatory authorities
- Qualified to Degree level or equivalent in Science.
- Membership of appropriate professional body.
- Registration as a Qualified Person, with acceptability to the Licensing Authority
- Significant experience in a senior Quality role with experience as a Quality Leader in a modern manufacturing environment within the pharmaceutical industry desirable.
- The ability to work effectively with peers, partners and others, to positively impact performance.
Our clients aim is to be a global leader in generics and biopharmaceuticals, improving the lives of patients across the world.
Location:
This role is based at our clients site in Runcorn.
Apply:
For more information, or to apply for this Quality Qualified Person role please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).
Please note:This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
It is essential that applicants hold entitlement to work in the UK
