Regulatory Affairs/Quality Assurance Officer

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.

• 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.

• 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.