Director, Regulatory Affairs CMC
$207k - $253kMadrigalpharma
## Director, Regulatory Affairs CMCApplylocations: MA - Waltham - Officetime type: Full timeposted on: Posted 3 Days Agojob requisition id: JR\_000763Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight against MASH. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra is the first and only medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). Our success is driven by our people. We are building a dynamic, inclusive, and high-performing culture that values scientific excellence, operational rigor, and collaboration. To support our continued growth, we are strengthening our workforce strategy to ensure we have the right talent, at the right time, in the right way.This role provides strategic, tactical and operational regulatory CMC leadership to support clinical trial applications, market registrations and post-approval submissions, along with managing the day-to-day regulatory CMC activities of assigned projects for development and/or commercial products. These activities include acting as a regulatory CMC representative on cross-functions teams, planning regulatory CMC submission strategies, and conducting regulatory CMC intelligence activities.**Key Responsibilities*** Independently develops and leads execution of regulatory CMC investigational, registration and/or post-approval strategies for assigned products.* Applies expert regulatory CMC knowledge to address and overcome challenges that arise during development and commercialization.* Guides the team in defining and driving the strategy for CMC regulatory dossier content and then reviews this content for conformance with established Health Authority requirements.* Represents the Madrigal Regulatory CMC function in Health Authority meetings and drives preparation activities for meetings with Health Authorities on CMC-related topics.* Provides global regulatory input and support to quality-related activities, including regulatory impact assessments for change controls, deviations and investigations.* Proactively identifies regulatory CMC risks, ensuring timely communication with line management.* Monitors, interprets and communicates relevant CMC-related global regulatory requirements, guidelines and emerging trends.**Required & Desired Qualifications*** BS in life sciences in a healthcare field or equivalent experience, advanced degree strongly preferred.* Minimum of 12 years relevant experience and 8-10 years’ regulatory CMC experience, along with broad-based CMC technical and product experience.* Strategic regulatory CMC experience with a proven track record in clinical, commercialization and life cycle management of small molecule products.* Demonstrated experience interacting with global health authorities on CMC topics.* Strong knowledge of regulations/guidelines governing global CMC development of pharmaceuticals is required.* Excellent communication skills and proven negotiation skills. Must be able to effectively communicate with technical SMEs at all levels and be able to present a scientific case to effectively communicate within the organization and/or regulatory agenciesMadrigal’s Total Rewards strategy is based on a biotech industry peer group comparator and is inclusive of base pay, bonus and equity. Our equity offers meaningful opportunity allowing our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization.All employees receive equity, which we believe reinforces our ownership culture. Base salary is determined by several factors including the candidate’s qualifications, skills, education, experience, business needs and market demands. As of the date of this posting, a good faith estimate of the current pay scale for this position, applicable to all candidates, is $207,000 - $253,000 per year. We comply with all applicable minimum wage laws.All full-time employees receive equity, which reinforces our ownership culture and offers meaningful opportunity for our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization. Full-time employees are also eligible for comprehensive benefits, including flexible paid time off, medical, dental, vision and life/disability insurance, and 401(k) offerings (i.e., traditional, Roth, and employer match) in accordance with applicable plans. We also offer additional voluntary benefits like supplemental life insurance, legal services, and other offerings. In addition, we offer mental health benefits through our Employee Assistance Program for employees and their family. The company also provides other benefits in accordance with applicable federal, state, and local laws. We are committed to providing reasonable accommodations for individuals with disabilities throughout the hiring process. If you need assistance, please contact View email address on click.appcast.io. Madrigal is an Equal Opportunity Employer. All employment is decided on the basis of qualifications, merit, and business need. Applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex gender identity, sexual orientation, national origin, age, disability, protected veteran or disabled status, or other characteristic protected by applicable federal, state, or local law. Unsolicited resumes from agencies should not be forwarded to Madrigal. Madrigal will not be responsible for any fees arising from the use of resumes through this source. Madrigal will only pay a fee to agencies if a formal agreement between Madrigal and the agency has been established. Applications are being accepted on an ongoing basis and can be submitted through our Madrigal Careers site. *Please be aware that we have received reports of individuals misrepresenting themselves as Madrigal Pharmaceuticals’ Hiring Managers, seeking to engage with job candidates through fraudulent online advertisements or job posting sites. These unauthorized individuals are using Madrigal’s name and logo in an attempt to solicit up-front fees and obtain personal information from interested job candidates. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process.* *Please also note that any correspondence with regard to employment would come from an authorized madrigalpharma.com email address or from an email address from one of our trusted search firm partners. We are aware that incorrect/fraudulent email addresses, with Madrigal misspelled, have been utilized in these most recent fraud attempts. If you receive unsolicited employment offers from people claiming to work for or on behalf of Madrigal, we recommend that you: do not respond to their questions; do not open any attachments; and do not click on any hyperlinks. Any questions regarding the legitimacy of job-related contacts can be directed to* *View email address on click.appcast.io**.* #J-18808-Ljbffr
$207k - $253k
...therapeutics for metabolic dysfunction‑associated steatohepatitis (MASH). This role provides strategic, tactical and operational regulatory CMC leadership to support clinical trial applications, market registrations and post‑approval submissions, and manages day‑to‑day...SuggestedFull timeFlexible hours$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...Suggested$290k - $323k
...follow the Company on LinkedIn and X. Lead and/or oversee global regulatory CMC submissions (e.g., INDs, CTAs, BLAs, MAAs etc.) through... ...S., Ph.D., etc.) required 12 years’ experience in Regulatory Affairs CMC in Pharma/Biotech Strong negotiation skills with health authorities...SuggestedTemporary workFor contractorsFlexible hours$170.9k - $231.3k
Overview The Associate Director, Regulatory Affairs CMC Development is responsible for developing and implementating global CMC regulatory strategies for development-stage programs. This role will play a critical part in shaping regulatory strategies for emerging therapeutic...SuggestedFull timeTemporary workWork at officeLocal areaFlexible hours$154.4k - $242.55k
...possible in order to bring life-changing therapies to patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows...SuggestedMinimum wageTemporary workLocal areaRemote workWorldwide$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$238k - $374k
...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...Minimum wageTemporary workWork at officeLocal areaRemote workWorldwide$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... ...in Chemistry, Biology, Pharmacy, Regulatory Affairs, Pharmaceutical Sciences, Engineering, or...Full timeSummer workRemote workFlexible hours2 days per week- ...Responsibilities: The Associate Director, Regulatory Affairs CMC will be responsible for leading regulatory CMC activities for Anagram’s portfolio of products, through all stages. Assist with developing Regulatory-CMC strategies and collaborating with key stakeholders...
- ## 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
- ...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...
$195k - $330k
...make an impact:Lead the development and execution of global regulatory CMC strategies for degrader programs across all stages of development... ...and submission readiness.Scale and lead the Regulatory Affairs CMC function as the pipeline and organization grow.Skills and...$196k - $240k
...mission to deliver 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...Local areaWorldwide- Kymera Therapeutics is seeking a Regulatory CMC leader to drive global CMC strategies across late-stage programs and coordinate submissions with FDA/EMA. You will author critical CMC content for INDs, CTAs, NDA/MAA and partner with Quality, Non-Clinical, and Clinical teams...
$242k - $313.5k
...for patients - realizing a world where people with immune‑mediated diseases can live life fully. Job Summary The Senior Director, Regulatory Affairs CMC - Biologics provides senior‑level scientific and strategic regulatory leadership for all Chemistry, Manufacturing, and...Local areaFlexible hours2 days per week- ...candidates for well-validated targets.Reporting to the Senior Director, Regulatory Affairs, the Associate Director, Regulatory Affairs will represent... ...to ensure cross-functional alignment, work with Regulatory CMC and Regulatory Operations teams to establish and meet...Temporary workWork at officeLocal areaImmediate start3 days per week
$270k - $310k
Department: 1310US - Regulatory - USLocation: Waltham, MACompany Overview:Dyne Therapeutics... ...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...Local area$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$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, driving the regulatory strategy for biologics and ATMPs in Biogen’s portfolio. Your role encompasses global, regional...Full timeTemporary workLocal area$182k - $275k
...is responsible for executing high-quality, science-based, and compliant regulatory CMC deliverables for assigned program(s), in alignment with strategies established by Global Regulatory Affairs and Technical Operations.This individual contributor role will execute regulatory...Work at office$134.2k - $202.2k
...MassachusettsShift: Department: HC-RD-RCD1 Reg CMC LM Marketed 1Recruiter: Sarah EllisThis... ....Your Role:The Senior Manager Regulatory CMC (RCMC) is responsible and accountable... ...worldwide, and serves as the Regulatory Affairs CMC contact point and acts as the liaison...Local areaImmediate startWorldwide$175k - $206.02k
Associate Director / Director, Regulatory Affairs About the Role We are seeking a highly skilled and experienced Associate Director / Director of Regulatory... .... Partner with Technical Operations to facilitate CMC gap analyses, regulatory impact assessments, and submissions...$204k - $245k
...personal and we approach every challenge with radical care. The Director, Regulatory CMC is responsible for leading execution of global CMC... ...industry experience, with relevant experience in CMC regulatory affairs for biologics or gene therapy products Experience...Full timeWork at officeFlexible hours3 days per week- Vertex Pharmaceuticals Inc is seeking a Director of Chemistry Manufacturing Controls (CMC) to lead a Regulatory CMC team responsible for global regulatory strategies and submissions across small molecule programs. The role emphasizes strategic leadership, Health Authority...
- Vertex Pharmaceuticals Incorporated in Boston is seeking a Chemistry Manufacturing Controls Manager to lead regulatory CMC activities for investigational and commercial products. You will review CMC submissions, develop global regulatory CMC strategies, and serve as the...
- Job DescriptionGeneral Summary:The Associate Director, CMC Quality Compliance and Inspection Readiness, is responsible for inspection readiness... ...and governance forumsKnowledge and Skills:Knowledge of regulatory requirements and inspection expectations globallyExperience...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
$174.5k - $274.23k
A leading biopharmaceutical company is seeking a Director Regulatory Site CMC in Boston, MA. The role focuses on regulatory change control and post-approval activities, ensuring compliance across diverse modalities. Candidates should have over 10 years of experience in...- Genetix Biotherapeutics is looking for a Director, Regulatory CMC to lead global regulatory strategies for gene therapy products. This full-time... ...and a strong background in CMC regulatory affairs, demonstrating exceptional communication and project management...Full time
- Rhythm Pharmaceuticals, Inc. is seeking an experienced Regulatory CMC professional to execute high-quality, compliant CMC deliverables for... ...contributor role collaborates with Global Regulatory Affairs, Technical Operations, and Quality to ensure timely, complete...
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