Quality and Validation Lead in Central Bedfordshire
Green Life Science is looking for an Quality and Validation Lead in Central Bedfordshire
Job description
Quality System Support
- Support implementation and maintenance of the Quality Management System (QMS) in accordance with ISO 9001 and/or ISO 13485.
- Assist in managing controlled documents, including SOPs, policies, forms, and validation records.
- Participate in internal audits and help prepare for external audits and regulatory inspections.
Validation Support
- Assist in the preparation, execution, and documentation of equipment qualification (IQ/OQ/PQ), process validation, and cleaning validation activities.
- Maintain accurate and organized validation files and records.
- Track validation timelines and help ensure activities are performed in compliance with internal procedures.
Compliance and Documentation
- Review completed documentation for accuracy, completeness, and compliance with applicable standards.
- Support investigations for deviations, non-conformances, and CAPAs related to validation and quality activities.
- Help maintain calibration and maintenance records for critical equipment.
Collaboration & Training
- Work closely with production, engineering, and quality control teams to support operational needs.
- Participate in training programs related to cGMP, ISO standards, data integrity, and validation principles.
Extra information
- Status
- Open
- Education Level
- Secondary School
- Location
- Central Bedfordshire
- Type of Contract
- Part-time jobs
- Published at
- 30-10-2025
- Full UK/EU driving license preferred
- No
- Car Preferred
- No
- Must be eligible to work in the EU
- No
- Cover Letter Required
- No
- Languages
- English
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