Senior Regulatory CMC Manager

JR United Kingdom; Milton Keynes; On-site; GBP 50,000 - 80,000; Full time

Job summary

A leading life sciences recruiter is looking for a Sr. Regulatory Chemistry, Manufacturing, and Controls Manager in Milton Keynes. This role involves leading a team to ensure regulatory compliance and managing the lifecycle of pharmaceutical products. Candidates should possess a bachelor's degree and expertise in relevant regulatory frameworks.

Qualifications

• Expertise in regulatory classifications including drugs, dietary supplements, or medical devices.
• Understanding of regulatory frameworks applied throughout the product lifecycle.
• Experience in managing submissions for various dosage forms.

Responsibilities

• Develop and implement strategies for regulatory compliance.
• Oversee creation and review of regulatory documents.
• Manage risks associated with product lifecycle maintenance.

Skills

Regulatory Compliance

Leadership

Strategic Planning

Document Review

English Proficiency

Education

Bachelor's degree or higher in a relevant field

Job description

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Client:

Hobson Prior

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Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

10.06.2025

Expiry Date:

25.07.2025

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Job Description:

We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.

Hobson Prior is seeking a Sr. Regulatory Chemistry, Manufacturing, and Controls Manager to lead a team focused on managing the lifecycle of pharmaceutical products in the EMEA region. This role emphasizes regulatory compliance and strategic planning for product approvals.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Develop and implement strategies to ensure regulatory compliance for product approvals.
• Identify necessary documents and address any issues related to content, quality, or timelines for submissions.
• Oversee the creation and review of regulatory documents, ensuring they meet global standards and timelines.
• Manage risks associated with product lifecycle maintenance and communicate strategies and issues to teams.
• Lead interactions with health authorities, including preparing for meetings and negotiations.
• Foster a culture of excellence by guiding and developing team members and collaborating with other departments.
• Build strong partnerships with research, operations, and local regulatory teams.

Key Skills and Requirements:

• Bachelor's degree or higher in a relevant field.
• Expertise in regulatory classifications such as drugs, dietary supplements, or medical devices.
• Understanding of regulatory frameworks and ability to apply them throughout the product lifecycle.
• Knowledge of post-approval changes and requirements for global markets.
• Experience in managing submissions for various dosage forms.
• Strong leadership and coaching abilities.
• Proficiency in English.

For more information, please contact Henry LeLacheur.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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