Are you passionate about regulatory affairs and eager to help life-changing medical products reach the market? Our client is looking for a Regulatory Affairs Officer to support their team in guiding pharmaceutical, medical device and life sciences companies through complex regulatory landscapes. Key Responsibilities Assist in preparing and submitting regulatory documents for UK, EU and US markets Support clinical trial processes, registries and Post-Market Clinical Follow-up studies Research evolving regulatory frameworks to keep strategies cutting-edge Work alongside senior consultants to develop tailored compliance solutions Requirements A degree in Life Sciences, Pharmaceutical Sciences, Regulatory Affairs or a related field An understanding of clinical trials, registries, and PMCF requirements Familiarity with global regulatory bodies and frameworks Strong IT skills and attention to detail Excellent communication and problem-solving abilities Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.