Director Regulatory CMC - Cell Therapy

Bristol Myers Squibb; Uxbridge; On-site; GBP 80,000 - 120,000; Full time

Job summary

A leading pharmaceutical company is seeking a Director for Regulatory CMC in Cell Therapy to oversee regulatory submissions and strategy development. This senior role involves working closely with global teams and health authorities to ensure compliance and drive innovation in cell therapy products. With a focus on collaboration and regulatory expertise, the position offers a significant opportunity to impact patient lives through science in a dynamic work environment.

Qualifications

• Minimum 10+ years of experience in the Pharmaceutical industry.
• Strong knowledge of CMC regulatory requirements.
• Ability to manage multiple complex projects.

Responsibilities

• Lead matrix teams for cell therapy products.
• Manage regulatory submissions for global markets.
• Provide strategic guidance for marketing applications.

Skills

Regulatory knowledge

Project management

Communication

Strategic thinking

Education

10+ years in Pharmaceutical industry

Knowledge of biotechnology / cell therapy

Tools

Electronic regulatory systems

Job description

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Director Regulatory CMC - Cell Therapy, Uxbridge

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Client:

Bristol Myers Squibb

Location:

Uxbridge, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

21d24f777c63

Job Views:

5

Posted:

02.06.2025

Expiry Date:

17.07.2025

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Job Description:

Description

The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of a products lifecycle. Members of the organization develop global regulatory CMC strategies and partners with key stakeholders to execute the strategies in alignment with business priorities. The team also perform regulatory assessments for manufacturing changes, provides guidance on regulatory expectations for medical devices, oversees BSE program & provides compliance documents to support Health Authority submissions. The team also supports Medical Information to build/maintain database to address external questions regardingdrug products.

Position Summary

The CMC Regulatory Director, Cell Therapy is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support Cell Therapy products regarding: Clinical trial applications; New marketing applications; HA responses & background packages (including participating/leading HA meetings);&/or post-approval submissions. In this role, theGRS-CMC Director, Cell Therapy will serve as the primary interface between Global Regulatory Sciences and Biometrics (GRSB) & Cell Therapy Development Operations (CTDO). The GRS-CMC Director will assess Manufacturing Change Controls for global impact &guide technical teams on practical aspects of global change management.

Position Responsibilities

·Represent regulatory CMC on and/or lead matrix teams for cell therapy pipeline products and/or commercial products through completion of post-marketing commitments & relevant lifecycle management projects driven by research

·Independently provide strategic guidance/input related to current regulatory requirements and expectation for biologics/cell therapy marketing applications, clinical trial applications for projects, and/or lifecycle changes to marketed products.

·Independently manage and prioritize multiple complex projects

·Interface with the Health Authorities for CMC submissions and CMC-related issues, with guidance and oversite from supervisor on complex topics.

·Identify, communicate and propose resolutions to routine/complex issues

·Interpret global regulations and guidance. Identify regulatory opportunity and risks.

·Anticipate and communicate possible regulatory paradigm shifts

·Participate inproduct fact finding meetings

·Review and provide regulatory assessments on change controls

·Prepare and manage CMC submissions for all global markets while ensuring thoroughness, completeness and timeliness, including creation and maintenance of strategy documents

·Mange relationships with diverse teams

·Utilize electronic systems for dossier creation and tracking.

Requirements

·Minimum of 10+ years Pharmaceutical industry experience – prefer knowledge of biotechnology / cell therapy products, including multi-disciplined experience, 8+ years CMC regulatory strategy (biologics/cell therapy experience preferred).

·Knowledge of CMC regulatory requirements during development and post-approval. Experience with global CMC regulations for biological/cell therapy compounds preferred.

·Knowledge of biopharmaceutical development, including biological drug substance and sterile drug product and analytical methods. Expertise in the cell therapy drug development process and analytical methods, preferred.

·Demonstrated ability to develop/maintain strong working relationships with the regulatory CMC team and cross functional teams, participate on and/or lead multifunctional teams, handle and prioritize multiple projects and work independently.

·Ability to identify, communicate and resolve complex issues.

·Prepare and manage filings and ensure thoroughness, accuracy and timeliness.

·Ability to interpret global regulations and guidance.

·Strong oral and written skills.

·Proficient with electronic systems

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb is Disability Confident – Committed