
Specialist, QA
- Cheshire Stockport, Greater Manchester
- Permanent
- Full-time
- Ensuring site compliance with regulations and internal Procedures
- Supporting the QA Manager in management of site Quality Management System(QMS) and Quality Key Performance Indicators (KPIs)
- Self Identification and correction of Quality issues.
- Continuous Improvement through CAPA and Change Control Management
- Quality Disposition / Risk Management
- Supporting Audits
- Development and Approval of Standard Operating Procedures
- Investigation of deviations through Non-conformance.
- Approval of NCR investigations, Product Complaints and Micro deviations.
- Mentoring and coaching of new QMS record owners.
- Minimum of 3 yrs experience in quality team facilitation, project management, process improvement or quality data analysis role.
- Minimum 3 yrs experience in Pharmaceutical, Medical Device, Biotechnology, Chemistry, Microbiology or other related regulated industry.
- Proven knowledge of Quality System processes (essential), with working knowledge of current EU and UK GMP requirements (EU GMP Volume 4 Annex 1) (preferred), or experience of working within ISO 9001, ISO 13485, MDD 93/42/EEC, or similar regulations and standards (considered).
- Experience of coordinating and supporting Document Control, Internal Audit, CAPA, Non-conformance and Complaints processes (required).
- Experience of problem solving using Root Cause Analysis techniques such as 8D, GEMBA, 5 Whys, Cause and Effect (required).
- Internal / Lead Auditor experience.
- Working knowledge and hands on experience of software tools to manage Quality Systems processes such as TrackWise (required).
- Competitive total compensation package
- Professional development opportunities
- High importance placed on work life balance
- Commitment to growing and developing an inclusive and diverse workforce