GMP Compliance Specialist - Pharma Manufacturing

Full Job Description

Passionate about Pharma GMP? Are you a key voice in the QA department?

• Fantastic opportunity to influence the quality culture
• Hertfordshire based

Verbatim Pharma are looking for a GMP Compliance Specialist to play a pivotal role in delivering sound guidance to the Manufacturing department.

Not only will you draw on your attention to detail, but passion for getting things right first time.

Some core duties and skills you will cover daily:

• Final review of manufacturing batch records for completeness, accuracy and compliance before submission to QA and QP for batch release
• Coordinate document reviews, approvals, and revisions in collaboration with cross-functional teams.
• Take overall control of closing deviations, CAPAs, change controls, investigations and risk assessments and act as the liaison between the manufacturing and Quality Assurance department in this regard.
• Assist in the preparation for regulatory inspections by organising and providing necessary documentation.
• Train staff on quality related procedures and best practices and ensure training matrix and training records are up to date for the manufacturing team
• To support and train production staff in raising, investigating and closing our of Quality records or issues (CAPAs, deviations, etc.)

If you'd like to understand a little more, please apply!

Commutable locations:

Radlett / Aylesbury / Rickmansworth / Chesham / Amersham / St Albans / Berkhamsted / Apsley / Borehamwood / Barnet / Northwood / Watford / Ruislip / High Wycombe / Wembley / Harrow / Greenford / Slough / Welwyn Garden City / London / Watford

Related job titles:

Compliance Manager / Good Manufacturing Practice / Document Controller / Document Control/ Quality Manufacturing Advisor / Quality Operations Specialist / Quality Compliance Manager