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Regulatory Cmc Associate
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Regulatory Affairs CMC Manager
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Regulatory Affairs Manager CMC
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CK Group Uxbridge, United KingdomCK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. · Company: · Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses b ...
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CMC Regulatory Affairs Manager
1 week ago
Park Street People Uxbridge, United KingdomJob DescriptionOur client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. · This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence ...
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Regulatory Affairs CMC Manager
1 week ago
Cpl Life Sciences Uxbridge, United KingdomJob Description · Job Title: Regulatory Affairs CMC Manager · Job Type: 6-Month Contract (inside IR35) · Location: Uxbridge or Cambridge – 1 day on-site per month · Rate: £45 to £55 per hour (PAYE) · An exciting opportunity to join a leading global pharmaceutical company on a ...
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Regulatory Affairs CMC Manager
1 week ago
Cpl Life Sciences Uxbridge, United KingdomJob Title: Regulatory Affairs CMC Manager · Job Type: 6-Month Contract (inside IR35) · Location: Uxbridge or Cambridge – 1 day on-site per month · Rate: £45 to £55 per hour (PAYE) · Scroll down to find the complete details of the job offer, including experience required and as ...
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CMC Regulatory Affairs Manager
1 week ago
Park Street People Uxbridge, United KingdomOur client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. · This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly ...
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CMC Regulatory Affairs Manager
1 week ago
Park Street People Uxbridge, United KingdomOur client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. · This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly ...
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Regulatory Affairs CMC Manager
5 days ago
Cpl Life Sciences Uxbridge, United KingdomJob Title: Regulatory Affairs CMC Manager · Apply now, read the job details by scrolling down Double check you have the necessary skills before sending an application. · Job Type: 6-Month Contract (inside IR35) · Location: Uxbridge or Cambridge – 1 day on-site per month · Rate ...
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Regulatory Affairs CMC Manager
1 week ago
Cpl Life Sciences Uxbridge, United KingdomJob Title: Regulatory Affairs CMC Manager · Job Type: 6-Month Contract (inside IR35) · Location: Uxbridge or Cambridge – 1 day on-site per month · Rate: £45 to £55 per hour (PAYE) · An exciting opportunity to join a leading global pharmaceutical company on a 6-month basis a ...
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Regulatory Affairs CMC Manager
1 week ago
Cpl Life Sciences Uxbridge, United KingdomJob Title: · Regulatory Affairs CMC ManagernJob Type: · 6-Month Contract (inside IR35)nLocation: · Uxbridge or Cambridge – 1 day on-site per monthnRate: · £45 to £55 per hour (PAYE) · An exciting opportunity to join a leading global pharmaceutical company on a 6-month basis and s ...
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Regulatory Affairs Manager CMC
1 week ago
CK Group- Science, Clinical and Technical Uxbridge, United KingdomCK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. · Company: · Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses b ...
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CMC Regulatory Affairs Manager
1 week ago
Park Street People Uxbridge, United KingdomOur client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. · This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly ...
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Regulatory Affairs Manager CMC
1 week ago
CK Group- Science, Clinical and Technical Uxbridge, Greater London, United Kingdom £45.02CK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. · Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by ...
Director Regulatory CMC - Uxbridge, United Kingdom - Bristol Myers Squibb
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 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); &/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 & 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 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
·Mange relationships with diverse teams
·Utilize electronic systems for dossier creation and tracking.
Requirements
·Minimum BA/BS Degree
·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 scienceTM ", 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
A UK Government scheme