Regulatory Affairs CMC Consumer

TN United Kingdom; High Wycombe; Hybrid; GBP 50,000 - 80,000; Full time

Job summary

An established industry player in Consumer Health is seeking a Regulatory Affairs professional for a hybrid contract role in High Wycombe. This exciting opportunity involves leading a team to ensure successful product registrations and managing regulatory deliverables across drugs, dietary supplements, and medical devices. With a focus on operational excellence and cross-functional collaboration, you will play a key role in driving regulatory objectives. Flexible working options are available, making this a great chance for those looking to advance their career in a dynamic environment.

Benefits

Flexible working options

Qualifications

• Strong knowledge of EU and EMEA regulatory frameworks.
• Experience in managing regulatory deliverables for drugs and medical devices.

Responsibilities

• Lead a Regulatory Affairs team for product registrations and line extensions.
• Manage global regulatory deliverables in alignment with business objectives.

Skills

Regulatory Affairs knowledge

Pharmaceutical CMC expertise

Cross-functional collaboration

Education

Degree in Life Sciences or related field

Job description

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Regulatory Affairs CMC Consumer, High Wycombe

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Client:

Location:

High Wycombe, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

9ddc9b87d3db

Job Views:

5

Posted:

02.05.2025

Expiry Date:

16.06.2025

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Job Description:

Your 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 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.
Creates 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, with expertise across a broad spectrum of Regulatory classifications including Drugs, Dietary Supplements, and Medical Devices, mainly pharmaceutical CMC regulatory affairs.

What you'll get in return
Flexible working options available.