A leading medical technology company in Basingstoke seeks a Regulatory Affairs Specialist to support global regulatory submissions for its medical device portfolio. The role involves authoring technical documentation, liaising with authorities, and contributing to post-market surveillance. Candidates should have a degree in Regulatory Affairs or similar and at least 2 years of relevant experience. Strong skills in regulatory compliance, internal auditing, and attention to detail are essential. The position may require occasional travel for audits and compliance activities.
#J-18808-Ljbffr