A pioneering life sciences organization in Cambridge is seeking a Regulatory Affairs Manager to lead regulatory strategy and execution throughout the product lifecycle. The role involves managing submissions, overseeing post-market activities, and mentoring junior talent. Candidates should have over 5 years of experience in regulatory affairs, particularly in IVD or medical devices. A competitive salary package and benefits are on offer. #J-18808-Ljbffr
Regulatory Affairs Manager (IVD) – Lead EU Submissions employer: Arevna
Arevna Partners is an exceptional employer for Private Client Solicitors, offering a supportive and flexible work environment across multiple UK locations, including London, Manchester, and Birmingham. With competitive salaries, achievable bonuses, and clear pathways for career advancement, employees benefit from a balanced culture that prioritises manageable workloads and professional growth, making it an ideal choice for those seeking meaningful and rewarding legal careers.
