Production Compliance Coordinator
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Location | Hertfordshire |
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Job Type | Permanent |
Blackfield Associates are currently supporting a leading pharmaceutical manufacturing organisation in the search for a Production Compliance Coordinator to join their Production Operations team on a permanent basis.
This is an excellent opportunity for an organised and detail-oriented professional looking to develop their career within a highly regulated GMP manufacturing environment. The successful candidate will play a key role in supporting production compliance activities, ensuring manufacturing operations continue to meet quality, regulatory, and operational standards.
Responsibilities
As Production Compliance Coordinator, you will work closely with Manufacturing, Quality, Technical, and EHS teams to support compliance across production operations. You will be responsible for coordinating quality system activities, maintaining controlled documentation, supporting investigations, and driving continuous improvement initiatives.
This is a day-based position supporting a manufacturing operation operating across multiple shifts.
- Coordinate and track Production Quality Management System activities to ensure ongoing compliance.
- Create, review, and update production batch documentation.
- Author and maintain SOPs and training records in collaboration with subject matter experts.
- Support quality and risk assessment activities, including QRA and EHS assessments.
- Manage and follow up CAPAs, action items, and effectiveness checks.
- Participate in quality investigations and deviation management activities.
- Support internal audits, inspections, and compliance-related initiatives.
- Work collaboratively across Production, Quality Assurance, Technical Services, HR, and EHS functions.
- Contribute to continuous improvement projects that enhance compliance, efficiency, and operational performance.
- Ensure all activities are conducted in line with GMP, GDP, company procedures, and industry regulations.
Requirements
- Strong attention to detail and excellent documentation skills.
- Good organisational and administrative abilities.
- Effective written and verbal communication skills.
- The ability to build positive working relationships across departments.
- Strong prioritisation and time management skills.
- A proactive and collaborative approach to problem-solving.
- Competency with Microsoft Office applications.
- Knowledge of GMP regulations and pharmaceutical manufacturing environments would be advantageous.