International Pharmaceutical Manufacturer requires a QA Officer to work on a 4 on 4 off rotating shift pattern. The main purpose of this role is to assist in prompt handling of quality incidents, deviations, customer complaints using Trackwise; maintain compliance to quality systems through auditing, training as required; review of Batch Process Records.
Reporting to the QA Operations Team Leader, the post holders responsibilities will include:
·Being a QA contact across site throughout shift.
·Receiving, reviewing and processing quality reports on Trackwise (e.g. DR/QI/CAPA records) according to defined procedures.
·Requesting, discussing and agreeing actions in response to a range of quality records including deviations, complaints and control changes as required.
·Ensuring that any documents presented for QA approval/checking are complete
·Ensuring a standard approach to quality systems throughout the facility
·Ensuring concerns regarding product safety and quality are drawn to the attention of colleagues and appropriate staff, including QA Management.
·Reviewing Batch Process Records, media fill records, autoclave records.
·Participating as required in Regulatory and customer audits.
You will be joining a leading specialist Manufacturer experiencing significant growth internationally, with excellent opportunities for career development.
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