Your new companyA leading Consumer Health company is looking for a contractor within Regulatory Affairs CMC. This is a 6-month hybrid contract job with scope for extension.Your new roleLeads a Regulatory Affairs team ensuring the success of new product registrations, line extensions and new indications and claims with supportive technical justification/documentation in alignment with the business plan.Create an environment of operational excellence through regulatory expertise by managing direct reports and collaborating with cross-functional teams to successfully achieve regulatory objectives.Manages the global &/or regional regulatory deliverables for drugs, dietary supplements & medical devices as relevant, within their brand area & geographic responsibility.Develops strong partnerships with Regulatory Affairs Franchise, R&D, Marketing, Supply Chain and local business representatives.Represents the Regulatory Affairs CMC function as appropriate in Self Care Franchise, functional and business leadership teams.What you'll need to succeedRegulatory Affairs knowledge across EU and wider EMEA and expertise across a broad spectrum of Regulatory classifications including Drugs, Dietary Supplements and/or Medical Devices, mainly pharmaceutical CMC regulatory affairs.What you'll get in returnFlexible working options available.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 us for a confidential discussion on your career.
Back to searchRegulatory Affairs CMC Consumer contract job
Hays Specialist Recruitment Limited
Posted 21 hours ago, valid for 4 days
High Wycombe, Buckinghamshire HP12 4HS, England
Full Time
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Sonic Summary
- A leading Consumer Health company is seeking a contractor for a 6-month hybrid position in Regulatory Affairs CMC, with potential for extension.
- The role involves leading a Regulatory Affairs team to ensure successful new product registrations and managing global regulatory deliverables for drugs, dietary supplements, and medical devices.
- Candidates should possess Regulatory Affairs knowledge across the EU and EMEA, along with experience in pharmaceutical CMC regulatory affairs.
- The position offers flexible working options and requires collaboration with various teams including R&D, Marketing, and Supply Chain.
- Salary details are not specified, but the role typically requires several years of relevant experience in the regulatory field.
