Regulatory Affairs CMC Consumer
JOB_53132354681499Job type
ContractLocation
High WycombeWorking Pattern
Flexible Working,Full-timeSpecialism
Regulatory AffairsIndustry
PharmaceuticalsPay
£75 - £85 umbrella rate
Regulatory Affairs CMC, pharma, dietary, medical devices, combination, contract job
Your new company
A 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 role
Leads 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 succeed
Regulatory 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 return
Flexible working options available.
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 on your career.
A 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 role
Leads 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 succeed
Regulatory 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 return
Flexible working options available.
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 on your career.
Regulatory Affairs CMC ConsumerJOB_531323546814992025-04-252025-07-25
Talk to Victoria Dunlop, the specialist consultant managing this position
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JOB_53132354681499