Associate Director, Regulatory Affairs CMC

JR United Kingdom; Newport; Remote; GBP 60,000 - 90,000; Full time

Job summary

A leading life sciences consultancy is looking for an Associate Director of Regulatory Affairs - CMC. This role involves leading regulatory strategies, managing client relationships, and directing project teams in a dynamic remote environment. You'll leverage your extensive regulatory expertise to guide biotech clients through complex global submissions and support their strategic goals across biologics development.

Benefits

Fully remote, flexible working environment

Career progression in a collaborative consultancy

Exposure to cutting-edge biologics

Qualifications

• 8–12 years of experience in CMC Regulatory Affairs, particularly with biologics.
• Track record of leading global regulatory submissions.
• Strong scientific understanding of drug development processes.

Responsibilities

• Develop and implement CMC regulatory strategies for biologics.
• Serve as primary regulatory contact and manage client projects.
• Oversee preparation and submission of regulatory applications.

Skills

Regulatory Affairs

Client Management

Communication

Project Leadership

Stakeholder Management

Job description

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Associate Director, Regulatory Affairs CMC, newport

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Client:

AL Solutions

Location:

newport, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

A fast-growing and forward-thinking life sciences consultancy is seeking an Associate Director of Regulatory Affairs – CMC to lead regulatory strategy and execution across a dynamic portfolio of biologic and advanced therapy programs. This fully remote opportunity is ideal for an experienced, client-facing regulatory professional ready to make a broader strategic impact.

As an Associate Director, you will work directly with biotech clients across early- and late-stage development, taking the lead on CMC regulatory activities and guiding project teams through global regulatory pathways.

Key Responsibilities:

• Lead the development and implementation of CMC regulatory strategies for biologics across development and post-approval stages
• Serve as the primary regulatory point of contact for client projects and Health Authority interactions
• Oversee preparation, review, and submission of INDs, IMPDs, BLAs, MAAs, variations, and supplements
• Contribute to internal regulatory intelligence and advise cross-functional teams on evolving regulatory expectations
• Support strategic client engagements, including proposal development and consultation meetings
• Mentor and guide junior regulatory team members on CMC-related matters

Your Profile:

• 8–12 years of experience in CMC Regulatory Affairs, with strong biologics expertise (e.g. mAbs, cell/gene therapy, ATMPs)
• Proven track record leading global submissions across the product lifecycle
• Strong scientific understanding of drug development, manufacturing, and quality systems
• Previous experience in a consultancy, CRO, or agile biotech environment is highly desirable
• Excellent communication and stakeholder management skills, including client-facing interactions
• EU-based preferred, but global applicants with relevant experience will be considered

What’s On Offer:

• Associate Director-level role with strategic influence across multiple client programs
• Fully remote, flexible working environment
• Exposure to cutting-edge biologics and global regulatory frameworks
• Career progression in a collaborative, fast-paced consultancy
• Opportunity to work with top-tier clients across the EU and US markets