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Your new company:
Join a leading organisation in the Self Care franchise, dedicated to developing and implementing regulatory strategies across the EMEA region. They are committed to ensuring the success of new product registrations, line extensions, and new indications and claims for drugs, dietary supplements, and medical devices.
Your new role:
As a Regulatory Affairs CMC Consultant, you will provide regulatory input and technical guidance to product development teams. You will be responsible for supporting the development of the CMC Regulatory strategy in EMEA. You will be responsible for preparing and submitting regulatory CMC submissions, maintaining compliance with local regulatory and quality system requirements, and managing a team to achieve regulatory objectives. The focus will be on securing new product registrations, extending existing product lines, and obtaining approvals for new indications and claims.
What you'll need to succeed:
- Expertise in regulatory classifications, including drugs, or dietary supplements.
- Minimum of 6 years of regulatory CMC Experience for EMEA
- Strong project management skills.
What you'll get in return:
- An opportunity to make a significant impact on the Self Care franchise.
- 6-month contract with scope to extend
- Attractive rate on offer
What you need to do now:
If 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 us for a confidential discussion about your career.Feel free to let me know if you need any further adjustments or additional details!
