Regulatory CMC Director
3 weeks ago
Bristol Myers Squibb is seeking a highly skilled Regulatory CMC Director to join our team. As a key member of our Global Regulatory Sciences organization, you will be responsible for developing and implementing global regulatory strategies for biologics and cell therapy products. This is a unique opportunity to work with a talented team of professionals who are passionate about transforming patients' lives through science.
Key Responsibilities- Develop and implement global regulatory strategies for biologics and cell therapy products
- Collaborate with cross-functional teams to ensure regulatory compliance and effective product development
- Provide regulatory expertise and guidance to internal stakeholders on CMC-related matters
- Prepare and submit regulatory filings and responses to health authorities
- Stay up-to-date with global regulatory requirements and trends in the biopharmaceutical industry
- Minimum 10+ years of experience in regulatory affairs, with a focus on biologics and cell therapy products
- Proven track record of developing and implementing successful regulatory strategies
- Strong knowledge of global regulatory requirements and trends in the biopharmaceutical industry
- Excellent communication and collaboration skills
- Ability to work in a fast-paced environment and prioritize multiple tasks and projects
Bristol Myers Squibb is committed to creating a diverse and inclusive work environment that fosters innovation and collaboration. We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and talented individual who is passionate about regulatory affairs, we encourage you to apply for this exciting opportunity.
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Regulatory CMC Director
4 weeks ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeJob SummaryBristol Myers Squibb is seeking a highly skilled Regulatory CMC Director to join our team. As a key member of our Global Regulatory Sciences organization, you will be responsible for developing and implementing global regulatory strategies for biologics and cell therapy products. This is a unique opportunity to work with a talented team of...
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Regulatory CMC Director
4 weeks ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeJob SummaryBristol Myers Squibb is seeking a highly skilled Regulatory CMC Director to join our team. As a key member of our Global Regulatory Sciences organization, you will be responsible for developing and implementing global regulatory strategies for biologics and cell therapy products. This is a unique opportunity to work with a talented team of...
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CMC Regulatory Expert
2 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeJob SummaryThe CMC Regulatory Director will serve as the primary interface between Global Regulatory Sciences and Biometrics, and will be responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support Cell Therapy products.Key ResponsibilitiesRepresent regulatory CMC on and/or lead matrix...
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CMC Regulatory Expert
2 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeJob SummaryThe CMC Regulatory Director will serve as the primary interface between Global Regulatory Sciences and Biometrics, and will be responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support Cell Therapy products.Key ResponsibilitiesRepresent regulatory CMC on and/or lead matrix...
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CMC Regulatory Director Cell Therapy
1 week ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeJob SummaryThe CMC Regulatory Director, Cell Therapy is responsible for developing and implementing global regulatory CMC strategies for cell therapy products. This includes content development, compilation, maintenance, and review of the Quality Module for regulatory submissions.Key ResponsibilitiesRepresent regulatory CMC on and/or lead matrix teams for...
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Director Regulatory CMC
5 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeDescription 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...
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CMC Regulatory Director for Cell Therapy
2 weeks ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeJob SummaryThe CMC Regulatory Director for Cell Therapy will be responsible for developing and implementing global CMC regulatory strategies for cell therapy products. This includes content development, compilation, maintenance, and review of the Quality Module for regulatory submissions.Key ResponsibilitiesRepresent regulatory CMC on and/or lead matrix...
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Uxbridge, United Kingdom Bristol Myers Squibb Full timeTransforming Patients' Lives through ScienceBristol Myers Squibb is a leading pharmaceutical company that is dedicated to transforming patients' lives through science. We are seeking an experienced CMC Regulatory Associate Director to join our team in Global Regulatory Sciences.Job SummaryThe CMC Regulatory Associate Director will be responsible for...
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Uxbridge, United Kingdom Bristol Myers Squibb Full timeTransforming Patients' Lives through ScienceBristol Myers Squibb is a leading pharmaceutical company that is dedicated to transforming patients' lives through science. We are seeking an experienced CMC Regulatory Associate Director to join our team in Global Regulatory Sciences.Job SummaryThe CMC Regulatory Associate Director will be responsible for...
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Associate Director, Global Regulatory Sciences-CMC
5 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
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Associate Director, Global Regulatory Sciences
5 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
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Global Regulatory CMC Lead
4 weeks ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeLead Regulatory Strategy for Innovative BiologicsBristol Myers Squibb is seeking a highly motivated and experienced Global Regulatory CMC Lead to join our dynamic team. In this role, you will play a pivotal part in shaping the regulatory landscape for our pipeline of groundbreaking biologics. Your Impact:Spearhead regulatory CMC efforts for both...
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Global Regulatory CMC Lead
2 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeLead Regulatory Strategy for Innovative BiologicsBristol Myers Squibb is seeking a highly motivated and experienced Global Regulatory CMC Lead to join our dynamic team. In this role, you will play a pivotal part in shaping the regulatory landscape for our pipeline of groundbreaking biologics. Your Impact:Spearhead regulatory CMC efforts for both...
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Sr Associate Regulatory Affairs
5 months ago
Uxbridge, United Kingdom Amgen Full timeCareer Category Regulatory **Job Description**: - Job Description: - Amgen is a leading human therapeutics company in the biotechnology industry. For more than 40 years, the company has tapped the power of scientific discovery and innovation to advance the practice of medicine. As a Fortune 500 company serving millions of patients. Amgen continues to be...
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Director, Regulatory Affairs
4 months ago
Uxbridge, United Kingdom Parexel Full timeWhen our values align, there's no limit to what we can achieve. We are seeking a highly skilled and experienced Regulatory Affairs Director to join our team. As a Director, you will be responsible for the successful execution of multiple projects and ensuring client satisfaction. You will provide mentorship, leadership and direction to Managers and...
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Regulatory Sciences Associate Director
2 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeAbout the RoleWe are seeking a highly skilled Regulatory Sciences Associate Director to join our Global Regulatory Sciences (GRS) team at Bristol Myers Squibb. As a key member of our team, you will be responsible for providing regulatory expertise related to CMC activities throughout the product lifecycle.Key ResponsibilitiesDevelop and implement global...
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Regulatory Sciences Associate Director
2 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeAbout the RoleWe are seeking a highly skilled Regulatory Sciences Associate Director to join our Global Regulatory Sciences (GRS) team at Bristol Myers Squibb. As a key member of our team, you will be responsible for providing regulatory expertise related to CMC activities throughout the product lifecycle.Key ResponsibilitiesDevelop and implement global...
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CMC Regulatory Lead for Cell Therapy
2 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeAbout the Role We are seeking a highly motivated and experienced CMC Regulatory Lead to join our growing team focused on cell therapy products. In this role, you will play a pivotal part in ensuring the successful development and commercialization of innovative cell therapies by providing expert guidance on regulatory CMC strategies and submissions. Your...
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CMC Regulatory Lead for Cell Therapy
2 months ago
Uxbridge, United Kingdom Bristol Myers Squibb Full timeAbout the Role We are seeking a highly motivated and experienced CMC Regulatory Lead to join our growing team focused on cell therapy products. In this role, you will play a pivotal part in ensuring the successful development and commercialization of innovative cell therapies by providing expert guidance on regulatory CMC strategies and submissions. Your...
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Principal Regulatory Affairs Consultant
2 months ago
Uxbridge, United Kingdom Parexel Full timeWhen our values align, there's no limit to what we can achieve. Parexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong...