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QA Officer
This job has expired, and cannot be applied for.
- Posted By: JHR
- Address:
- Contact: 0113 383 3738
- Date Posted: 13th Oct 2008
- Salary: £25,000-£28,000
- Location: Leeds
- Reference Code: AG/2565
- Views Since Posting: 44
- Full Description:
QA Officer Manufacturing Support role
An exciting opportunity to join a leading company within an excellent role and team. This position reports to the QA Manager.
Main Function/Responsibilities of the Job
•To perform QA activities required ensuring that quality standards are achieved and maintained within all areas of the Company.
•To maintain internal GMP inspection system.
•To undertake batch documentation review, product release and oversight of manufacturing facility systems.
•Provide support to manufacturing by proactive involvement in Quality Improvement Plan, compliance upgrade projects and product quality investigations.
•Represent quality on site wide and departmental initiatives.
•Manage the Site GMP Training System.
•Co-ordinate and complete investigations for product quality complaints.
Primary Tasks
•To assure the quality of finished products to company quality standards by checking the in-process controls and adherence to procedures.
•To maintain company quality systems.
•Production checks and monitoring.
•Filling and Packaging Clearance approval – provide a final sign off and authorisation for each packaging clearance activity before the start of a production batch.
•Deviation control – review requested deviations from written manufacturing instructions, and approve as appropriate before and after they happen.
•Preparation and approval of batch specific manufacturing instructions – approval of batch specific information in manufacturing master documentation and release of approved master copies to manufacturing.
•Final review and approval of production records and release of product – final sign off and approval of manufacturing records (prior to the QP certification).
•Quality investigations – complete quality investigation reports for incidents associated with manufacturing and warehousing.
•Returns – performing inspection of returned goods prior to return to sock.
•Internal audit schedule – scheduling, performing and reporting audits against cGMP and QMS standards.
•Departmental representative on weekly and monthly manufacturing review meetings.
•Organise and manage the site GMP training system by enrolling new users, allocating training assignments and reporting monthly statistics.
•Be responsible for the Quality complaints system, receive, investigate and report all complaints.
In addition to the duties and responsibilities listed, the jobholder is required to perform other duties assigned by your Area Manager from time to time.
Health & Safety
To ensure that safe working practices are followed within all areas of your responsibility, to safeguard the health and wellbeing of yourself, your colleagues and the safety and protection of Company manufactured products.
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