Project Manager, CMC Regulatory Affairs

TN United Kingdom; Ware; On-site; GBP 55,000 - 75,000; Full time

Job summary

A leading biopharma company is seeking a Project Manager for CMC Regulatory Affairs in Ware. The role involves managing regulatory activities for drug development, ensuring compliance, and collaborating with cross-functional teams to drive project success. Ideal candidates will have a background in life sciences and experience in regulatory affairs. Join a company committed to improving patient health and fostering a supportive work environment.

Qualifications

• Two or more years of experience in CMC regulatory affairs.
• Experience in drug development and manufacturing processes.

Responsibilities

• Responsible for global CMC regulatory activities for assigned projects.
• Develop CMC strategy for submission documents.
• Ensure regulatory compliance and high-quality standards.

Skills

Chemistry

Regulatory Affairs

Project Management

Education

BS in Life Sciences

MS in Life Sciences

Job description

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Project Manager, CMC Regulatory Affairs, Ware

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Client:

1925 GlaxoSmithKline LLC

Location:

Ware, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

be891aa775eb

Job Views:

3

Posted:

17.05.2025

Expiry Date:

01.07.2025

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Job Description:

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong tech-enabled capabilities that allow us to build a deeper understanding of the patient, human biology and disease mechanisms, and transform medical discovery. We are revolutionising the way we do R&D. We’re uniting science, technology and talent to get ahead of disease together.

The Project Manager, CMC Regulatory Affairs will be responsible for the CMC regulatory activities in the investigational, late phase development and/or early commercial lifecycle management of GSK products.

Key Responsibilities:

• Responsible for the global CMC regulatory activities for assigned projects and responds readily to changing events and priorities.
• Responsible for CMC strategy development, with managerial support, for CMC submission documents from early phase clinical submissions (IND/IMPD) through to marketing applications (NDA/BLA/MAA) and early lifecycle management activities in accordance withthe applicable regulatory& scientificstandards
• Understands, interprets and will sometimes advise teams on regulations, guidelines, procedures and policies relating to development, registration and manufacture of medicinal products, to expedite the submission, review and approval of global CMC applications.
• Ensures all appropriate CMC regulatory aspects for clinical trials/product release are in place, to avoid clinical holds and/or to ensure continuity of market supply. Ensures information submitted in clinical/marketing applications meets regional requirements, allowing maximum Supply/Production/Quality flexibility with minimal unanticipated questions.
• Works in cross-functional matrix project teams, which include colleagues from regulatory, development, quality and manufacturing ensuring adequate interaction and partnership in order to define proper regulatory CMC filing strategy.
• Maintains high quality standards and seeks to raise levels of performance through continuous improvement and an innovative approach in responding to the evolving regulatory environment.
• Ensures regulatory compliance is maintained and sharesbest-practices and learnings within the CMC Regulatory teamsand other impacted functions.
• Engages inCMCSubject Matter Expert activities internally (for increased compliance,harmonisationand efficiency)
• Will sometimes deliver CMC regulatory strategy to support major inspections (egPAIs) with managerial support

Basic Qualifications:

• BS in a Life Sciences or related field.
• Two or more years of experience in Chemistry, Manufacturing and Controls (CMC) regulatory affairs orproduct development experience with direct involvement in regulatory submission preparation across all stages of development through to early life cycle submissions.
• Two or more years of experience in drug development, manufacturing processes and supply chain and may have a specialized area of expertise

Preferred Qualifications:

• MS in a Life Sciences or related field.
• RAPS Certification
• Pre-approval experience (phase 1 to phase 3 submission experience)
• Knowledge of worldwide CMC regulatory requirements and successful track record of delivering dossiers that comply with these, particularly for new medicines in development.

Please visit to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK.