Director, Global Regulatory CMC - Gene Therapy
Initial Therapeutics, Inc.
Lilly is seeking an experienced Regulatory CMC leader to develop and implement global CMC strategies for gene therapy programs. You will lead the preparation of CMC sections for IND/CTA, BLA/MAA submissions and serve as the primary liaison with major health authorities. The role requires 5+ years in regulatory CMC for ATMPs, strong leadership, and collaboration with R&D, Manufacturing, Quality, and Clinical teams. Excellent communication skills and deep knowledge of ICH guidelines are essential. #J-18808-Ljbffr Initial Therapeutics, Inc.
- Genetix Biotherapeutics is looking for a Director, Regulatory CMC to lead global regulatory strategies for gene therapy products. This full-time hybrid position based in Somerville, Massachusetts involves managing post-approval regulatory strategies and ensuring compliance...SuggestedFull time
$177k - $278.08k
...unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic... ...to patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute...SuggestedMinimum wageTemporary workLocal areaRemote workWorldwide$238k - $374k
...organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four... ...-changing therapies to patients worldwide.As Executive Director, Global Regulatory Affairs CMC Devices and Drug-Device Combination Product, you will provide...SuggestedMinimum wageTemporary workWork at officeLocal areaRemote workWorldwide$163.5k - $281.6k
...a highly experienced and strategic Director/Senior Director, Regulatory CMC to lead and execute regulatory CMC strategies for our cutting-edge gene therapy portfolio. This role will be critical... ..., ensuring compliance with global health authority requirements.Job ResponsibilitiesDevelop...SuggestedFor contractorsWork at officeFlexible hours$204k - $245k
...Director, Regulatory CMC Somerville, MA At Genetix Biotherapeutics every role has meaning, every... ...a company that's pursuing curative gene therapies to give patients and their families... ...responsible for leading execution of global CMC regulatory strategies for approved...SuggestedFull timeWork at officeFlexible hours3 days per week$163.5k - $281.6k
...truly matters for patients, we invite you to join us. Responsibilities Develop and implement comprehensive global regulatory CMC strategies for assigned gene therapy programs, including IND/CTA, BLA/MAA, and post-approval submissions. Lead and manage the preparation,...Full timeFor contractorsWork at officeFlexible hours$212k - $318k
...medicines for Cystic Fibrosis (CF), Casgevy, a gene therapy for sickle cell disease and beta-... ...reach patients faster than ever before.The Director, T1D will serve as a T1D Market Access... ...and Gene Therapy (CGT) portfolio in the Global Value and Access Strategy (GVAS) team....Full timeSummer workRemote workFlexible hours2 days per week$182k - $275k
Company OverviewRhythm is a global, commercial-stage biopharmaceutical company committed... ...-quality, science-based, and compliant regulatory CMC deliverables for assigned program(s),... ...more patients and developing novel therapies for other rare neuroendocrine diseases,...Work at office- ...Associate Director, Regulatory Affairs CMC Founded over a decade ago, CRISPR Therapeutics... ...developing transformative gene-based medicines for serious... ...world's first CRISPR-based therapy, approved for eligible... ...collaboration with CMC and global development teams, and with...Contract workRemote work
$238k - $374k
...all information I submit in my employment application is true to the best of my knowledge.Job DescriptionExecutive Director, Global Regulatory Affairs CMC Early DevelopmentAre you looking for a patient-focused company that will inspire you and support your career? Join...Minimum wageTemporary workLocal areaRemote work$190.4k - $285.6k
...Description General Summary: The Director, Chemistry Manufacturing Controls (CMC) leads a Regulatory CMC team responsible for developing and executing global regulatory strategies across multiple... ...pipeline of investigational therapies across a range of modalities in other...Summer workRemote workFlexible hours2 days per week- ...innovation and delivers transformative therapies to patients. By focusing R&D efforts... ...to patients worldwide. The Director, Regulatory Site CMC ensures efficient and compliant management... ...with strong practical experience with global HA requirements, beyond EU/US, who has...Local areaWorldwide
$242k - $313.5k
Senior Director, Regulatory Affairs CMC - Biologics About Beeline Medicines: Beeline Medicines is a clinical... ...category-leading precision therapies to transform the lives of people living... ...submitted in alignment with FDA, EMA, and global Health Authority expectations for...Local area2 days per week$212k - $333.19k
...innovation and delivers transformative therapies to patients. By focusing R&D... ...to patients worldwide. As Senior Director and Regulatory Platform Lead GRA CMC, Device and Drug‑Device Combinations... ...and proactive implementation. Globally influence and serve as a key opinion...Minimum wageFull timeTemporary workLocal areaWorldwideNight shift$268.2k - $402.2k
Job DescriptionGeneral Summary:The Executive Director, Regulatory Strategy will serve as a seasoned regulatory leader with expert technical and... ...overseeing the development and implementation of innovative global regulatory strategies for product development and...Full timeSummer workLocal areaRemote workFlexible hours2 days per week$177k - $278.08k
...organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic... ...bring life-changing therapies to patients worldwide.The Director Global Regulatory Affairs, Neuroscience is responsible for developing...Minimum wageTemporary workLocal areaRemote workWorldwide$241k - $332k
About This Role:As the Head of Regulatory CMC - Biologics & Advanced Therapy Medicinal Products (ATMP), you will lead a dynamic team within the PO&T function... ...ATMPs in Biogen’s portfolio. Your role encompasses global, regional, and local accountability for all therapeutic...Full timeTemporary workLocal area$142.5k - $256.5k
The Role:The Associate Director, Global Regulatory-CMC will be responsible for coordinating regulatory CMC activities for one or more products, depending on complexity, through all stages of a products lifecycle. The Associate Director will be responsible for developing...Permanent employmentFull timeWork at officeWork from home$290k - $323k
...a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline... ...LinkedIn and X. Responsibilities Lead and/or oversee global regulatory CMC submissions (e.g., INDs, CTAs, BLAs, MAAs etc.) through product...Contract workTemporary workFor contractorsFlexible hours$218.06k - $327.09k
Job Title: Senior Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Gaithersburg, MDBoston, MASouth... ...to role: Are you ready to set the global regulatory vision for pioneering... ...regulatory objectives with clinical, CMC, safety and commercial strategies....Hourly payFull timeTemporary workStart working todayWork at officeFlexible hours3 days per week$180k - $245k
...Therapeutics is seeking an experienced and strategic Director of Regulatory Affairs to lead and support global regulatory efforts across our development programs,... ...is required, and immunology background is preferred. CMC experience is a plus.ResponsibilitiesDevelop and...$142.5k - $256.5k
Role Overview The Associate Director, Global Regulatory-CMC will coordinate regulatory CMC activities for one or more products throughout their lifecycle, develop global regulatory CMC strategies, collaborate with stakeholders, and manage multiple projects to support the...$189k - $246k
...Department: 107000 Regulatory Location: San Diego... ...Remote Be a part of a global team that is inspired... ...deliver life-changing therapies to people living with... ...Position Summary: The Director, Regulatory Affairs... ..., Biostatistics, CMC, Quality, Nonclinical,...Temporary workLocal areaRemote workWeekend work$220k - $290k
...PACK delivered the first therapy specifically for women... ...U.S. and are exploring regulatory pathways for Europe and... ...term plans. The Senior Director, Regulatory Affairs has... ...update and implement a global regulatory strategy... ...development program. Guide CMC, nonclinical and...Temporary workFor contractorsWork at officeWeekday work$200k - $220k
...Director/ Senior Director, Regulatory CMC Join Us in Tackling Autoimmune Disease at Its Root At Vor, we believe... ...potential beyond one indication – a therapy that has already shown consistent results... ..., through clinical development and global registration. The candidate must be...Contract workWorldwideFlexible hours- Akebia Therapeutics seeks a Director, Regulatory Affairs - Labeling to shape global labeling strategy across our portfolio. You will serve as the enterprise expert... ..., Medical Affairs, Commercial, Legal, Safety, and CMC to ensure robust, compliant labeling. This senior...
- Beeline Medicines is seeking a Senior Director, Regulatory Affairs CMC - Biologics to lead regulatory science for biologics assets across the development lifecycle. You will drive global CMC strategy, author submissions, and coordinate with Process Development, Analytical...
- Associate Director, Global Regulatory Affairs, Advertising and Promotion Job Description At Takeda, we are a forward‑looking, world‑class R&D organization... ...that unlocks innovation and delivers transformative therapies to patients worldwide. The Associate Director, Global...Full timeRemote workWorldwide
$166.4k - $249.6k
Job DescriptionGeneral Summary:The Chemistry Manufacturing Controls (CMC) Associate Director leads and executes global regulatory CMC strategies across investigational and commercial products focusing on biologics. This role is accountable for authoring, reviewing, and...Full timeSummer workRemote workFlexible hours2 days per week$211.5k - $258.5k
Job Summary The Director, Regulatory Strategy - Global Regulatory Lead is responsible for developing and leading... ..., ensuring alignment with clinical, CMC, and non-clinical development... ...pipeline programs, including Breakthrough Therapy Designation (BTD), Fast Track Designation...Local areaFlexible hours2 days per week
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