🔎 Title: Regulatory Affairs Specialist📍 Location: Hybrid, Switzerland⌛ Contract length: Minimum 3 months⌛ Start date: Late August✉️ Contact: ahmed@elemed. eu🔸 The Opportunity: An IVD company is urgently seeking a Regulatory Affairs Specialist to support critical remediation activities. This is a high-impact contract where you’ll work directly with the leadership team to coordinate regulatory responses, align cross-functional teams, and guide submission strategy. This role is perfect for a contractor with strong IVD experience and deep knowledge of International (APAC, Middle East, Africa) regulatory frameworks who’s ready to step in and make an immediate impact. 🔹 Your responsibilities:
Coordinate regulatory remediation efforts and cross-team actionsProvide practical, compliant regulatory inputSupport project leadership in tracking timelines and action itemsParticipate in internal calls and regulatory discussionsWork closely with internal team members acting as project leads🔸 Your qualifications: Strong experience in IVD regulatory affairsDeep understanding of International regulatory requirements (APAC, Middle East, Africa)Experience working in regulated environmentExcellent project management and coordination skillsSelf-motivated, structured, and action-orientedFrench language skills are a bonus, but not essentialMust be available to start immediately and attend on-site as needed✉️ Interested in further conversation? Please send your CV to ahmed@elemed.
eu to arrange a confidential career discussion. 📲 Would you like to find out more about our open opportunities? Visit https: //www. elemed. eu/vacancies/🔎 Please note: Only candidates meeting the requirements set out in the role profile above will be considered in the application process. We spend a lot of time tailor writing our job descriptions to provide as much information as possible to prospective candidates. We’d appreciate if you’d also carefully review the profile and only apply if you meet the requirements set out in the description. 🩺 Elemed is Europe’s leading MedTech technical recruiter.
We serve within the Medical Device, Diagnostic and Combination Device arena, working with Managers up to VP of Quality and Regulatory. Our team helps medical device experts of today become leaders of tomorrow. ⚖️ We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
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