sasmar Verified 21h ago
Head of Quality and Regulatory Affairs
Ta' Xbiex, Malta On-site
Salary not listedPaySalary not listed
TypeFull-time
Work settingOn-site
Verified listing
JobFig found this opening at its original source and checks that it remains available.
About the role
We are committed to fostering an inclusive and diverse workplace that provides equal opportunities for all employees, and we are looking for someone who shares our values and vision for excellence.
What you'll bring
- A Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline
- Significant experience in Quality and Regulatory Affairs within the pharmaceutical or medical device sectors.
- Comprehensive understanding of global regulatory frameworks, including but not limited to FDA and EMA guidelines.
- Demonstrated leadership skills with experience managing diverse teams.
- Thorough knowledge of quality management systems, particularly ISO 13485 and other relevant certifications.
- Strong background in Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Experience in conducting regulatory audits and inspections is highly beneficial.
- Candidates MUST have permission to work in Malta, no permits offered for this role.
- Relevant certifications in quality management and regulatory affairs are preferred.
- an advanced degree is an asset.
Benefits
Medical Insurance