Job Description
About the Role
Reporting to the Head of Quality, you will play a key role in maintaining and enhancing Quality Management Systems (QMS) and ensuring compliance with relevant regulatory standards. You will work closely with cross-functional teams and act as the on-site Quality lead when required.
Key Responsibilities
- Maintain and improve QMS within a regulated manufacturing environment
- Oversee document control, deviations, CAPAs, and change management processes
- Support batch review and product release activities
- Conduct internal audits and assist with external and regulatory audits
- Lead investigations relating to quality issues, non-conformances, and complaints
- Drive continuous improvement initiatives across the business
- Provide training and guidance to operational teams on quality standards
About You
- Degree-qualified in Science, Life Sciences, or a related discipline
- Proven experience in a GMP-regulated environment
- Strong understanding of quality systems, compliance, and regulatory requirements
- Experience managing investigations and root cause analysis
- Excellent communication and stakeholder engagement skills
- Ability to manage competing priorities in a fast-paced setting
Are you interested in this position?
Apply by clicking on the “Apply Now” button below!
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