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, cosmetics and life sciences companies through complex regulatory landscapes.Whilst part of a team, you will work independently. Aside from regulatory submissions, you will engage with clients providing regular updates and advice on projects. This is a great opportunity to further develop your regulatory knowledge and consulting skills.Key ResponsibilitiesAssist in preparing and submitting regulatory documents for UK, EU and US markets mainly on medical devicesSupport clinical trial processes, registries and Post-Market Clinical Follow-up studiesResearch evolving regulatory frameworks to keep strategies cutting-edgeProvide updates, presentations and regular communication with clients across multiple time linesWork alongside senior consultants to develop tailored compliance solutionsRequirementsA degree in Life Sciences, Pharmaceutical Sciences, Regulatory Affairs or a related fieldAn understanding of clinical trials, registries, and PMCF requirementsExperience liaising with regulatory authorities and clients and presenting detailed reports to themFamiliarity with global regulatory bodies and frameworksStrong IT skills and attention to detailExcellent communication and problem-solving abilitiesPark Street People Ltd is an Equal Opportunities Employer. ..... full job details .....