Our client, a leading Pharmaceutical company, is looking to recruit a Regulatory Affairs/Quality Assurance officer to join their growing team.
The chosen candidate will report to the Responsible Person / Regulatory Affairs Manager, and will be responsible to:
- Maintain and support the company’s regulatory and quality systems in alignment with GDP and applicable regulations.
- Assist with medicinal product registrations, post-marketing surveillance, and pharmacovigilance activities.
- Implement and monitor compliance with medical device regulations in a proactive and timely manner.
- Ensure adherence to industry standards and internal policies to maintain product safety and efficacy.
- Collaborate with cross-functional teams to drive continuous improvement in regulatory processes.
Requirements
- Able to work on own initiative, as well as work within an established team to achieve goals.
- A can-do attitude and willing to learn.
- An eye for detail, excellent analytical and problem-solving skills
- Be strongly motivated and be able to meet the challenges of a fast-growing operation.
Education and Experience
- A Degree in Pharmacy or other science related Degree.
- Previous experience in regulatory affairs or a GMP / GDP environment is a must.
- Proficient in Excel, Word and other office software.
- Excellent spoken and written English.
- Must be acquainted with Maltese and EU regulatory framework and procedures.
Job Reference: JY691
