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Your new companyA global pharmaceutical and consumer health business is looking to take a regulatory affairs contractor with OTC expertise until March 2025. Your new roleYou will be responsible for the management of post-approval activities for OTC products. This is an EU focused role where you will be supporting the EMEA Regulatory team for activities for MRP/DCP products. You will be responsible for developing regulatory strategies and for preparing the applications and supporting maintenance activities where needed. What you'll need to succeed
- Have experience with OTC Medicines
- Expertise working with EMEA
- Minimum of 7-10 years of experience in regulatory affairs
- Short notice period, as this is a short contract, they do need to get someone in ASAP.
What you'll get in returnA competitive rate on offer, 2 days on site per week.What you need to do nowIf you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you, but you are looking for a new position, please contact Julia Bowden, Recruitment Manager, Regulatory Affairs Interim Recruitment.
