We are seeking a candidate to join our QA team to help drive quality in the company.  This is a UK office-based role, and you will work with the PQS system and drive compliance and timely closure for Deviations, Change Controls, CAPAs and Complaints.   You will be required to conduct investigations and root cause analysis for complaints and deviations. You will be required to have a good command of the English language in order to write summary reports. You will also prepare and review SOP’s and manage the electronic PQS trackers (trackers for Complaints, Deviations, Change Controls and CAPAs) – ensuring we are always on target for closure in our PQS. In this varied QA role, you’ll interact across all IPS departments providing real-time support to the teams – this might include attending functional meetings and resolving any quality issues.

To support the smooth running of the department, you’ll work closely with the existing team  and share the PQS workload and all other aspects of the Quality function which includes but is not limited to Technical Agreements, Vendor/Supplier Approvals, Supply Chain Approval for APIs and excipients  Post Implementation reviews,  temperature monitoring and writing reports, incident reviews BOM activation and inactivation of codes,  response to MHRA alerts /notifications, general document control etc., for which the Quality team are responsible .  Suitable candidates will receive more detailed training on the job.

 

The candidate will have excellent communication skills (both written and oral) which are important to the role and work well as a team member.

If you are interested in applying for this role please send your cover letter and CV to: HR@ips-pharma.com by 24th March 2023.