Executive Director, Regulatory Affairs CMC
$290k - $323kCrescent Biopharma
Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit and follow the Company on LinkedIn and X. Lead and/or oversee global regulatory CMC submissions (e.g., INDs, CTAs, BLAs, MAAs etc.) through product lifecycle. Proactively identify regulatory risks, opportunities, and mitigation strategies in alignment with objectives, and communicate to management, as needed Provide strategic regulatory guidance to TechOps and Quality organizations to ensure global compliance and readiness for clinical and commercial supply Serve as the primary interface with global regulatory agencies for CMC-related negotiations, milestone meetings, and information requests. Provides global regulatory input and support on product-compliance related activities including change controls, deviations, and investigations. Manage junior team members and contractors to support development activities BS/BA Degree in a Scientific Discipline, Advanced Degree (M.S., Ph.D., etc.) required 12 years’ experience in Regulatory Affairs CMC in Pharma/Biotech Strong negotiation skills with health authorities (e.g.FDA, EMA) as well as submissions Experience with leading IND and Marketing Applications Experience with antibody drug conjugates and biologics Strong analytical, strategic thinking, and problem-solving skills. Excellent communication and leadership abilities; able to influence across all levels of the organization. Ability to thrive in a fast-paced, ambiguous environment while managing competing priorities. Commitment to fostering a diverse and inclusive workplace Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment Competitive compensation, including base salary, performance bonus, and equity 100% employer-paid benefits package Flexible PTO; also, two, one-week company-wide shutdowns each year A commitment to your professional development, with access to resources, mentorship, and growth opportunities The salary range for this position is $290,000 to $323,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Additional Description for Pay Transparency The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation - Unlimited PTO; Sick time - 10 days per calendar year; Holiday pay, including two Company shut downs; Parental Leave - 16 weeks within one year of the birth/adoption/foster care of a child; FMLA; Military Leave. Additional information can be found - Crescent Biopharma is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status. #J-18808-Ljbffr Crescent Biopharma
$238k - $374k
...true to the best of my knowledge.Job DescriptionExecutive Director, Global Regulatory Affairs CMC Early DevelopmentAre you looking for a patient-focused... ...will inspire you and support your career? Join us as Executive Director, Global Regulatory Affairs CMC Early Development...SuggestedMinimum wageTemporary workLocal areaRemote work$238k - $374k
...we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.As Executive Director, Global Regulatory Affairs CMC Devices and Drug-Device Combination Product, you will provide strategic leadership and development to global regulatory...SuggestedMinimum wageTemporary workWork at officeLocal areaRemote workWorldwide$270k - $310k
Department: 1310US - Regulatory - USLocation: Waltham, MACompany Overview:Dyne Therapeutics... ...and Facebook.Role Summary:The Executive Director, Regulatory Affairs serves as a visionary leader who... ...related to clinical, nonclinical, and CMC development is critical Deep industry...SuggestedLocal area$207k - $253k
## Director, Regulatory Affairs CMCApplylocations: MA - Waltham - Officetime type: Full timeposted on:... ...tactical and operational regulatory CMC leadership to support clinical trial... ...*** Independently develops and leads execution of regulatory CMC investigational, registration...SuggestedMinimum wageFull timeLocal areaFlexible hours$207k - $253k
...MASH). This role provides strategic, tactical and operational regulatory CMC leadership to support clinical trial applications, market... ...projects. Key Responsibilities Independently develop and lead execution of regulatory CMC investigational, registration and/or post‑approval...SuggestedFull timeFlexible hours$190.4k - $285.6k
Job DescriptionGeneral Summary:The Director, Chemistry Manufacturing Controls (CMC) leads a Regulatory CMC team responsible for developing and executing global regulatory strategies across multiple... ..., Biology, Pharmacy, Regulatory Affairs, Pharmaceutical Sciences,...Full timeSummer workRemote workFlexible hours2 days per week$177k - $278.08k
...patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute... ...develops the regulatory CMC strategy and leads the execution of regulatory CMC investigational, registration...Minimum wageTemporary workLocal areaRemote workWorldwide$170k - $230k
Associate Director, Regulatory Affairs CMC Waltham, MA Skyhawk Therapeutics is seeking a hands‑on Associate Director, Regulatory Affairs CMC (RegCMC) to support the development and execution of the global RegCMC strategy for Skyhawk's small molecule pipeline. Working closely...$195k - $330k
...you’ll make an impact: Lead the development and execution of global regulatory CMC strategies for degrader programs across all stages of development... ...readiness. Scale and lead the Regulatory Affairs CMC function as the pipeline and organization grow....Full time$242k - $313.5k
...provide durable, life‑changing impact. Led by an established executive team and backed by world‑class life science investors,... ...diseases can live life fully. Job Summary The Senior Director, Regulatory Affairs CMC - Biologics provides senior‑level scientific and...Local areaFlexible hours2 days per week$196k - $240k
...functional improvement for individuals, families and communities. Role Summary The Director, Regulatory Affairs - Chemistry, Manufacturing, and Controls (CMC) is responsible for defining and executing global CMC regulatory strategies for Dyne programs across all stages of...Local areaWorldwide$170.9k - $231.3k
Overview The Associate Director, Regulatory Affairs CMC Development is responsible for developing and implementating global CMC regulatory strategies... ...PA office.Key ResponsibilitiesLead the development and execution of global CMC regulatory strategies for innovative small...Full timeTemporary workWork at officeLocal areaFlexible hours$241k - $332k
About This Role:As the Head of Regulatory CMC - Biologics & Advanced Therapy Medicinal Products (ATMP), you will lead a dynamic team within... ...strategy, technical development, and manufacturing execution. By leading multiple projects in a fast-paced environment, you...Full timeTemporary workLocal area$182k - $275k
...Opportunity OverviewThis role is responsible for executing high-quality, science-based, and compliant regulatory CMC deliverables for assigned program(s), in... ...with strategies established by Global Regulatory Affairs and Technical Operations.This individual contributor...Work at office$163.5k - $281.6k
...patients, we invite you to join us. Eli Lilly and Company is seeking 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 in shaping...For contractorsWork at officeFlexible hours$134.2k - $202.2k
...: Department: HC-RD-RCD1 Reg CMC LM Marketed 1Recruiter: Sarah... ...Your Role:The Senior Manager Regulatory CMC (RCMC) is responsible and... ...and serves as the Regulatory Affairs CMC contact point and acts as... ...coordination:Support development and execute initiatives Plans regulatory...Local areaImmediate startWorldwide- ...Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Manager Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients to deliver biologics...Work at officeLocal areaRemote work
- ...of Chemistry, Manufacturing & Controls (CMC) About the Company Well-financed, venture... ...for aligning CMC plans with clinical, regulatory, and corporate milestones, and will play... ...of CMC will be tasked with building and executing the CMC roadmap, overseeing technology...
$220k - $370k
...highly motivated and experienced Senior Director or VP of Regulatory Affairs. The ideal candidate will have a... ...Responsibilities: Lead the development and execution of the Company's Regulatory strategy... ...into clinical, nonclinical, CMC, quality, pharmacovigilance, medical...Summer workWork at officeFlexible hours- ...Alnylam Switzerland GmbH in Cambridge, MA is seeking an Associate Director, Regulatory Affairs CMC to lead the development and execution of global regulatory strategies for innovative therapeutics, particularly in CMC Development. This role combines scientific expertise...
- ## Associate Director, Regulatory Affairs CMCApplyremote type: Site Basedlocations: South Boston, MAtime type: Full timeposted on: Posted Todayjob... ...bring multiple novel therapies to patients. As the Regulatory CMC lead for these programs, you will have the opportunity to...Contract workRemote work
- ...seeks a Chemistry Manufacturing Controls Manager to oversee regulatory CMC submissions and strategic interactions with agencies. You will... ...readiness. The role requires a strong background in regulatory affairs, cGMP, and experience with Veeva for submissions....Remote work
- Vertex Pharmaceuticals Incorporated is seeking a Chemistry Manufacturing Controls Manager to lead regulatory CMC activities for both investigational and commercial products. The role involves reviewing CMC sections, developing global strategies, and coordinating with cross...
- Vertex Pharmaceuticals Incorporated seeks a Director of Chemistry Manufacturing Controls (CMC) to lead a Regulatory CMC team responsible for global regulatory strategies... ...decision-making, documentation, and submission execution. The role emphasizes strategic leadership,...
- Responsibilities: The Associate Director, Regulatory Affairs CMC will be responsible for leading regulatory CMC activities for Anagram’s portfolio... ...CMC strategies and collaborating with key stakeholders to execute the strategies in alignment with business priorities. Prepare...
$166.4k - $249.6k
...DescriptionGeneral Summary:The Chemistry Manufacturing Controls (CMC) Associate Director leads and executes global regulatory CMC strategies across investigational and... ...in Biology, Chemistry, Pharmacy, Regulatory Affairs, or related life science field (advanced degree preferred...Full timeSummer workRemote workFlexible hours2 days per week- Job DescriptionGeneral Summary:The CMC Quality Compliance Director is responsible for inspection readiness and compliance of internal and external... ...manufacturing/testing sites. Monitor and interpret cGMP regulatory guidelines and trends in the regulatory space and...Full timeWork experience placementSummer workRemote workFlexible hours2 days per week
$276k - $414k
Job Title: Executive Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Gaithersburg, MDBoston, MASouth San Francisco, CASanta Monica, CAIntroduction to role: Are you ready to set the global regulatory direction for first-in-class cell therapies...Hourly payFull timeTemporary workWork at officeWorldwideFlexible hours3 days per week- Rhythm Pharmaceuticals, Inc. is seeking an experienced Regulatory CMC professional to execute high-quality, compliant CMC deliverables for assigned programs... ...contributor role collaborates with Global Regulatory Affairs, Technical Operations, and Quality to ensure timely,...
- 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, authoring, and review of high-quality CMC sections for all regulatory submissions...For contractorsWork at office
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