QUALITY SYSTEMS SPECIALIST
| Employment Type | Permanent |
|---|---|
| Location | Hampshire , Hampshire |
| Industry Sector | Manufacturing |
| Start Date | asap |
| Salary/Rate | £30000 - £40000 per annum + Benefits |
| Reference | TP737 |
| Date Advertised | 14-08-2008 - 14:25 |
This vacancy is out of date and no longer accepting applications.
Description
Our Client packages and distributes Branded pharmaceuticals, OTC medicines and next-generation vaccine products throughout the world. Operating on behalf of three major brand names, the manufacturing output extends to 300 product lines at their 26 acre, state of the art manufacturing facility in Hampshire. They have the immediate requirement for a Quality Systems Specialist, to improve and implement quality systems across site.
Our Client packages and distributes Branded pharmaceuticals, OTC medicines and next-generation vaccine products throughout the world. Operating on behalf of three major brand names, the manufacturing output extends to 300 product lines at their 26 acre, state of the art manufacturing facility in Hampshire. They have the immediate requirement for a Quality Systems Specialist, to improve and implement quality systems across site. Candidates will have a scientific education (preferably Degree or equivalent) and experience in Quality Assurance or Quality Control in the Pharmaceutical Industry.
Job Summary:
•To improve and implement Quality Systems across site in line with corporate and regulatory requirements, ensuring SMEs fully understand QS requirements and provide site training where appropriate on Quality System matters.
•To assist in delivering site GXP training and maintain GXP training compliance.
•To act as the subject matter expert for designated Quality systems and support other SMEs as required.
•To support site inspections and provide technical expertise as required.
•To review and improve Quality Systems, and take part in effective training and roll-out of Quality System methodology. To facilitate effective GXP training compliance and training support for the Quality Unit, and to develop and implement a system to effectively achieve permanent inspection readiness.
•To introduce Quality metric visual displays across the quality organization in order to track and monitor progress and improvements and to ensure that Quality Systems are understood and implemented in compliance with regulatory/corporate expectations.
•To assist in comprehensively resolving, to the agreed timescales, inspection issues raised by self-inspection, internal (site and GCA) and external bodies.
•To gather, assess and report in a timely fashion all metrics required by the IMR process or GQO, related to the specific activities within the group.
•To provide appropriate assistance within and across the PPU and across other service departments in order to resolve issues and to ensure effective support and documentation of risk assessments.
•Provide technical support within the group, to the PPUs and external parties as required.
