Executive Director, Cell Therapy Regulatory CMC
Bristol Myers Squibb EU Policy
Bristol Myers Squibb EU Policy is seeking a Director for Regulatory CMC in Cell Therapy. In this role, you will oversee management of multiple development projects, represent GRS-CMC in cross-functional teams, and ensure compliance with regulatory requirements. The ideal candidate will have a minimum of 10 years of experience, including 8+ years in regulatory CMC, and possess strong leadership, negotiation, and scientific communication skills. Join us in making impactful contributions to advanced therapies. #J-18808-Ljbffr Bristol Myers Squibb EU Policy
- Bristol-Myers Squibb is seeking a Director, Regulatory CMC for Cell Therapy in Madison, NJ. In this pivotal role, you will oversee multiple development and lifecycle management projects, ensuring regulatory compliance and strategic direction in alignment with global guidelines...Regulatory
$255.48k - $309.59k
Executive Director, Worldwide Cell Therapy Medical Communications Lead The Executive Director, Medical Communications Lead is the Cell Therapy Medical... ...Medicine, Commercial, Market Access, Patient Safety, Regulatory, Quality, and Manufacturing/Supply, ensuring integrated...RegulatoryWorldwideFlexible hours- ...Technical Writer and Document Specialist in Summit, NJ, to support regulatory strategy for Cell Therapy clinical portfolios. This role demands effective collaboration across technical functions and management of CMC documentation for submissions. Successful candidates will...Regulatory
$255.48k - $309.59k
## Executive Director, Worldwide Cell Therapy Medical Communications LeadMadison - Giralda - NJ - USFind out how well you match with this job**Working... ...Research, Development, Medical, Commercial, Quality, Regulatory, Market Access, and Patient Safety to move with urgency...RegulatoryHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workWorldwideFlexible hoursShift work- Senior/Executive Director, Non-Clinical Drug Safety Evaluation Senior/Executive... ...clinical studies leading to regulatory filings, and provide support... ...process, including CMC, non-clinical and clinical and... ...clinical development of Oncology therapy products Excellent...RegulatoryFull timeFor contractors
- ...Assurance for our CAR T manufacturing site, ensuring compliance with regulatory standards while overseeing aseptic process validation and... ...strong leadership skills, and have previous experience in cell therapy. This position offers various benefits such as health...RegulatoryFlexible hours
$255k - $425k
Job Description Job Title: Executive Director, Head of Clinical Supply Planning and Operations... ..., we are advancing breakthrough therapies in oncology, cardiovascular disease,... ...TECH Unit sub‑functions (Project Lead (CMC), Regulatory Affairs CMC, Process Technology Research...RegulatoryTemporary work$40.97 - $49.64 per hour
Senior Specialist, QC Microbiology, Cell Therapy Position Summary: Responsible for supporting... ..., training, and transfer/validation. Execute document revisions, projects, deviations... ..., follow, interpret and apply Global Regulatory and cGMP requirements. Demonstrated technical...RegulatoryHourly payFull timeTemporary workSummer workFlexible hours- ...monitoring, and method validation. Ideal candidates will have substantial microbiological testing experience and a strong grasp of regulatory compliance. In addition to technical expertise, the position requires effective communication skills and the ability to work...Regulatory
- EmergencyMD is seeking a regulatory CMC specialist to provide global regulatory support throughout the product lifecycle in Morristown, New... ...high-quality CMC regulatory submissions and ensuring timely execution of corporate goals. The ideal candidate should possess a S/Ph...Regulatory
- ...and drive integrated program strategies aligned with clinical, regulatory, CMC, and commercial objectives. Contribute to rare disease... ...development plans, critical milestones, and cross-functional execution to ensure delivery against strategic objectives. Ensure accountability...RegulatoryWork at office
$40.97 - $49.64 per hour
...Specialist, QC Microbiology, Cell TherapySummit West - NJ - USFind... ...latest breakthroughs in cell therapy, this is work that transforms... ..., and transfer/validation. Execute document revisions, projects,... ..., interpret and apply Global Regulatory and cGMP requirements.•...RegulatoryHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$238.2k - $288.64k
...production line to the latest breakthroughs in cell therapy, this is work that transforms the lives... ....To lead a team of Quality Senior Directors or others in the oversight of the... ...stakeholders from MSQ, OPEX, Supply Chain, Regulatory, Project Management, and Operations....RegulatoryHourly payFull timeContract workTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work- In this position, the Regulatory Affairs CMC Director will lead the international Regulatory Affairs CMC team and support the development of sound... ...collaborate with development teams in China to develop and execute robust regulatory CMC strategies and risk migration for...Regulatory
$138.6k - $257.4k
Job Title Associate Director, Drug Supply Location and Relocation East Hanover, NJ,... ...will lead a critical function supporting Cell and Gene Therapy manufacturing operations, overseeing... ...Lean principles. Ensure compliance with regulatory, quality, safety, and business...RegulatoryRelocationRelocation package- ...Requires a high level of understanding of cell therapy processes (CAR-T), controls, and GMP... ...Implements training programs that meet regulatory requirements and business needs, including... ...the Clinical Program (as needed): Execute/Implement batch records in ISO 7 & 8 clean...RegulatoryTraineeshipLocal area
- ...Senior Vice President, Regulatory Affairs Location: Hybrid - Parsippany... ...by delivering innovative therapies that reduce reliance on... ...as a critical member of the Executive Leadership Team. Reporting directly... ...the CEO, ELT, and Board of Directors on regulatory risks,...Regulatory
- ...of care communities. As one of the nation’s largest contract therapy providers, Reliant offers unmatched clinical support, professional... ...treatment delivery models, ensuring care meets clinical and regulatory standards. Follow infection control and environmental safety...RegulatoryFull timeContract workReliefFlexible hours
- ...clinical team. Required Qualifications: Valid Physical Therapy license in compliance with state regulations Current BLS certification... ...to infection control protocols, safety guidelines, and regulatory standards while addressing patients’ comfort needs during...RegulatoryTemporary workWork from home
$141.5k - $268.5k
Associate Director, Regulatory Affairs Advertising & Promotion (Hybrid) Full-time Salary Min: 141500 Therapy Area: Neuroscience Salary Max: 268500 Workday Global Grade: 20 Compensation: USD 141,500 - USD 268,500 - yearly Responsibilities Make decisions and plans...RegulatoryFull timeTemporary work- ...interdisciplinary healthcare teams Maintain compliance with clinical, regulatory, and documentation standards Support quality improvement... ...Therapist License Graduate of an Accredited Physical Therapy Program Ability to work independently with strong clinical...RegulatoryWork from home
$285k - $300k
...governance excellence, organizational rhythm, and cross‑functional execution across all functions of the US business. The ideal candidate... ...Partner closely with Finance, Commercial, Medical, Regulatory, HR, and other functions to synthesize inputs, resolve roadblocks...RegulatoryFull timeWork at officeLocal area- ...What Will You Do:Conduct initial and periodic physical therapy evaluations to determine residents’ functional status and establish... ...and discharge summaries in accordance with facility policy and regulatory standards.What We Are Seeking:Graduate of a Physical Therapy curriculum...Regulatory
- ...biopharmaceutical company developing therapies for patients with serious... .... Reporting to the Senior Director, Biostatistics, this... ...programmers, data managers, regulatory, and clinical operations professionals... ...‑quality study design and execution. Work closely with...RegulatoryInterim roleLocal areaRemote work
$70 per hour
..., develop individualized treatment plans, and provide skilled therapy services to help patients restore function, improve mobility,... ...healthcare professionals to coordinate care Follow all organizational, regulatory, and clinical practice standards Requirements Active New...RegulatoryHourly payFull timeContract workPart timeMonday to FridayFlexible hours3 days per weekWeekday work- ...Responsibilities: Design and implement individualized occupational therapy plans for patients with a variety of diagnoses, including... ...safety Document patient progress and outcomes in accordance with regulatory guidelines and center policies About the Role: As an...RegulatoryFull time
- ...along with a commitment to delivering consistent, high-quality therapy services in a dynamic setting. Key Responsibilities: Implement... ...organized treatment environment Ensure compliance with all regulatory and company standards Qualifications: Associate degree from an...RegulatoryFull timePart time
$1,782 - $1,896 per week
...other duties as assigned within the scope of practice Adhere to hospital safety protocols, infection control guidelines, and regulatory standards Required Essential Skills: Critical thinking, service excellence, and good interpersonal communication skills...RegulatoryFull timeContract workTemporary workShift work$60 per hour
...techniques and equipment. Maintain compliance with safety and regulatory standards. Perform other duties as assigned. Additional... ...Education: Graduate of an accredited occupational therapy program. Experience: Experience in inpatient rehab preferred...RegulatoryHourly payTemporary workPart timeRelief$206.25k - $343.75k
...US Senior Medical Director, Rare Hematology Location... ...(wAIHA), and Sickle Cell Disease (SCD) among other... ..., Clinical Research, Regulatory, Science, Marketing,... ...advisory boards Lead execution of the strategic U.S.... ...rare hematology therapies Review Educational...Regulatory
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