Client:
Bristol Myers Squibb Location:
Uxbridge, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
21d24f777c63 Job Views:
92 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of a product's lifecycle. Members of the organization develop global regulatory CMC strategies and partner with key stakeholders to execute the strategies in alignment with business priorities. The team also performs regulatory assessments for manufacturing changes, provides guidance on regulatory expectations for medical devices, oversees BSE program, and provides compliance documents to support Health Authority submissions. The team also supports Medical Information to build/maintain a database to address external questions regarding drug 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); and/or post-approval submissions. In this role, the GRS-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 and 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 expectations 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 oversight from supervisor on complex topics. Identify, communicate and propose resolutions to routine/complex issues. Interpret global regulations and guidance. Identify regulatory opportunities and risks. Anticipate and communicate possible regulatory paradigm shifts. Participate in product 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. Manage 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. 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
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Bristol Myers Squibb Location:
Uxbridge, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
21d24f777c63 Job Views:
92 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of a product's lifecycle. Members of the organization develop global regulatory CMC strategies and partner with key stakeholders to execute the strategies in alignment with business priorities. The team also performs regulatory assessments for manufacturing changes, provides guidance on regulatory expectations for medical devices, oversees BSE program, and provides compliance documents to support Health Authority submissions. The team also supports Medical Information to build/maintain a database to address external questions regarding drug 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); and/or post-approval submissions. In this role, the GRS-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 and 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 expectations 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 oversight from supervisor on complex topics. Identify, communicate and propose resolutions to routine/complex issues. Interpret global regulations and guidance. Identify regulatory opportunities and risks. Anticipate and communicate possible regulatory paradigm shifts. Participate in product 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. Manage 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. 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
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