Cmc regulatory Work, Jobs (with Salaries)

Regulatory Consultant - CMC (CMC with small molecule products)
サイネオス・ヘルス —Remote
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- Bachelor's degree
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Regulatory Affairs Consultant - CMC vax/bio (home or office based)
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Global Regulatory CMC Scientist (UK)
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- Master's degree
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CMC Biopharma Regulatory Consultant — Ecolab Life Sciences
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- Doctoral degree
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Regulatory Scientist
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Bachelor's degree
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Quick apply
Senior Regulatory Affairs Specialist
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- Hybrid work
- English
- Bachelor's degree
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DT Lead, Single Systems - CMC Development Sciences (UK)
UCB —Slough
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Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International plc —Marlow
- £80,000 - £140,000 a year
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RA/CMC Specialist
Siemens Healthineers —London
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1d
Associate Director, Global Regulatory Science, CMC
Moderna, Inc. —London
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
Associate Director, CMC Regulatory Science, International
Moderna, Inc. —London
- Full-time
- Doctoral degree
- Master's degree
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Senior Scientist, Analytical Development
Replimune —Abingdon
- Full-time
- Doctoral degree
- Computer literacy
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10d
Senior Regulatory Specialist
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- IT
- Annual leave
Quick apply
Regulatory Affairs Executive
Sandoz —Bracknell
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- Project management
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Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International —Marlow
- £66,814 - £134,641 a year
- Full-time
- Bachelor's degree
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- Leadership
Quick apply
Sr. Principal Scientist, Advisor, Sr. Advisor of Global Regulatory Affairs Chemistry, Manufacturing & Controls and Devices-EMEA
Eli Lilly —Bracknell
- Full-time
- Doctoral degree
- English
- Master's degree
14d
Director, Regulatory Pre-Award Strategy - Europe/Canada- Remote
Worldwide Clinical Trials —England
- Full-time
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- English
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- In-person
Associate Director, CMC Regulatory Affairs, International
Moderna, Inc. —London
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
CMC Associate Director
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- Management
- Project management
- IT
- Annual leave
Quick apply

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Regulatory Consultant - CMC (CMC with small molecule products)

サイネオス・ヘルス
Remote

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Job details

Qualifications

Biology
Bachelor's degree
Contracts

Full job description

Updated: July 29, 2026
Location: Remote, LND, United Kingdom
Job ID: 25108623

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Description

Regulatory Consultant - CMC (CMC with small molecule products)

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

General Position Summary

The Chemistry Manufacturing Control Consultant will support the execution of multi-product global regulatory CMC for marketed products for small molecule products. Biologics / Cell and Gene Therapy experience. This role contributes to the preparation and submission of regulatory CMC documentation and provides regulatory support to various cross functional teams.

Key Duties and Responsibilities

Execute commercial Lifecycle Management (LCM) strategy and submissions with a focus on Middle East and North Africa or LATAM
Reviews CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies for small molecule products
Works with regulatory colleagues in development of global regulatory CMC strategies and Submissions
Participates effectively on cross-functional teams and may serve as the primary regulatory CMC contact for assigned products and projects

Required Education Level & Experience

Bachelor's degree, with a preference in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another related life-science field
Typically requires 4 years of experience in the pharmaceutical industry or related field, or the equivalent combination of education and experience
Preferred experience supporting Small Molecule programs

Required Knowledge/Skills

Strong interpersonal skills to exchange complex information with others and to guide others
Ability to collaborate and communicate in an open, clear, complete, timely and consistent manner
Strong sense of planning and prioritization, and the ability to work with all levels of management

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Apply Now

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cmc regulatory jobs

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