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A leading pharmaceutical company in the UK is seeking a Quality Assurance professional to support cGMP activities and ensure compliance with regulatory standards. The role entails working with a multidisciplinary team to ensure timely delivery of patient and hospital orders. Candidates should possess at least 2 years of GMP experience. The company offers attractive benefits, including annual leave, bonuses, and a pension plan.
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 amodernmanufacturing 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.
Reporting to Quality Assurance Operations Team Leader and Senior Quality Assurance Officers , this role will combine Quality focussed cGMP activities (supporting production output via worksheet checking and final batch release) with a broad range of Pharmaceutical Quality System activities (E. G. deviation/complaint primary investigations and root cause analysis).
Working alongside a multi-disciplinary team, the job holder will ensure that the services provided by themselves (and the company as a whole) result in patient & hospital orders being delivered on‑time/in‑full so that treatments can be carried out safely and at appointed times. All completed tasks and actions must comply with the requirements of the relevant regulatory authority (MHRA).
At least 2 years experience in GMP (or similarly regulated). Awareness of COSHH.role(s).