*Handling of day to day activities related to operations and quality systems, this includes but is not limited to, the handing of complaints, deviations, change controls, technical agreements, stability programs (monitoring and assessment), product specification files, batch documentation, batch release, PQR's.
*Lead and follow up on investigations and CAPA's implementation and effectiveness
*Liaising with CMO's (Contract Manufacturing Organisations) and other contractors inside and outside of the EU
*Support the QA department in maintaining the QMS in good order
*Support other internal departments as and when required
*Candidates are required to have a degree in life sciences (minimum bachelor degree, ideally masters or above)
*Post qualification experience of working in a similar position would be an advantage
*Ideally some previous experience within QA.
The right candidate will also have:
*An enthusiastic, confident and self-motivated personality and the ability to quickly contribute to the culture and way of working
*Excellent attention to detail (essential)
*Computer literate and numerate (essential)
*Ability to work in a team environment
*Ability to work under pressure and meet deadlines
*Able to work in autonomy and demonstrate engagement and ability to use initiative
Benefits Include -
*Annual bonus (non-contractual, subject to company and individual performance)
*Pension scheme (up to 10% employer contribution)
*25 days annual leave
This is a great opportunity to join a fantastic team. Apply now.
- CAPA's - QMS - GMP
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