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STEM & Life Science Courses › SE51D Carlow Master of Science Pharmaceutical Regulatory Affairs
Regulatory & Pharmacovigilance

SE51D Carlow Master of Science Pharmaceutical Regulatory Affairs

South East Technological University

Career prospects

[Opportunities for graduates from this programme include progression to Level 10 (PhD) programmes in related fields of study. According to a report from the Forfás Expert Group on Future Skills Needs, Ireland is emerging as a leading location for biopharmaceuticals with a mix of start-ups, high growth SMEs and large multinationals located here. Industry leaders including Pfizer, EliLilly, Sanofi, MSD (biologics based in Carlow) and Alkermes plc. have significant investment in Ireland which has facilitated rapid growth and development of the industry. These coupled with a strong generics industry (Wockhardt,Clonmel Healthcare both based in the South-East) provide prospective employment opportunities for graduates and key engagement partners for the programme. More than 85 pharmaceutical companies (including nine of the top 10) operate over 100 facilities in Ireland. The industry exports around$85 billion worth of products each year and is now one of the largest exporters of pharmaceuticals in the world.]

Entry requirements

[A second-class honours degree in science, engineering, quality, pharmaceutical or regulatory affairs or cognate areas. Those failing to meet the classification requirement may be eligible for entry to the Postgraduate Diploma. Candidates with significant experience in: pharmaceutical operations, quality engineering, device design, mid to senior management in industry, other professionals who wish to upskill in the regulatory affairs environment, regulatory affairs personnel themselves who want to upskill (as determined by the Institutes recognition of prior learning policy), in addition to an honours primary degree in another discipline area may also be considered for entry. International Applications]

Where this leads
Regulatory & Pharmacovigilance

Getting and keeping products approved — regulatory affairs submissions, compliance, and drug-safety/pharmacovigilance.

€55,000 – €68,000 mid-career, up to €135,000 at senior manager level
Source: Life Science Recruitment, Salary & Market Trends Report 2026; cross-ref Morgan McKinley Ireland 2026
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Course facts

LocationWaterford
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