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$190.4k - $285.6k
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$170.9k - $231.3k
## Associate Director, Regulatory Affairs, CMCUnited StatesApply NowFind out how well you match with this jobJob ID3315This role is considered:Hybrid**Overview**The Associate Director, Regulatory Affairs CMC Development is responsible for developing and implementating...SuggestedFull timeTemporary workWork at officeLocal areaFlexible hours$238k - $374k
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...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$170k - $220k
Associate Director, Regulatory CMC - Solid Biosciences Charlestown, MA HQ Solid Biosciences is a precision genetic medicine company focused on... ...preferred. Minimum of 4 years of experience in regulatory affairs in the pharmaceutical/biotech, including IND activity, global...Full timeTemporary workRemote workFlexible hours$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...Work at office$270k - $350k
The Senior Director, Regulatory Affairs is responsible for planning, developing, and implementing regulatory strategy, submissions, and compliance... ..., design, and implementation of clinical, nonclinical, and CMC regulatory strategy—including preparation, submission, and...Shift work$212k - $333.19k
...the boundaries of what is possible in order to bring life‑changing therapies to patients worldwide. As Senior Director and Regulatory Platform Lead GRA CMC, Device and Drug‑Device Combinations Human Factors, you will provide leadership for the development and implementation...Minimum wageFull timeTemporary workLocal areaWorldwideNight shift- ...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 products...Full timeWork at officeLocal areaRemote work
- ...Job Title: Executive Director, Global Regulatory Affairs Department: Regulatory Affairs Reports To: Vice President, Regulatory Affairs / Sr. Vice President... ...closely with Clinical Development, Clinical Operations, CMC/Technical Operations, Nonclinical, Biometrics, Medical...
- ...Hemab seeks a Director, Regulatory Affairs who will be responsible for developing and executing innovative global regulatory strategies for the global... ...-quality content yourself. You bring expertise in global CMC regulatory requirements and approach challenges with...Work at office
$248k - $280k
...Massachusetts. For more information, visit Position Purpose: The Director, Global Regulatory Strategy will be responsible for developing and delivering... ...Skills & Experience: 8+ years minimum of Regulatory Affairs experience in the pharmaceutical industry. S., M.S. or Ph...Full timeTemporary work- ...s research and development is focused on understanding and meeting patient needs using our novel therapies. Tasks The Director of Regulatory Affairs provides strategic and operational leadership to the development and commercialization of products for one or more of the...
$189k - $246k
Department: 107000 Regulatory Location: San Diego, USA- Remote Position Summary The Director, Regulatory Affairs Strategy is responsible for developing and executing global regulatory... ..., Medical Affairs, Biostatistics, CMC, Quality, Nonclinical, Commercial, and Executive...Temporary workLocal areaRemote workWeekend work$245k - $300k
...Biosciences is seeking an experienced and strategic Senior Director, Regulatory Affairs to lead and execute global regulatory strategies across our... ...Pharmacology, Clinical Operations, Biostatistics, Pharmacovigilance, CMC, Nonclinical, Quality, and Executive Leadership to advance...Local area$200k - $240k
...Associate Director, Regulatory Affairs Operations At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively...Work at officeLocal area- .... Job Description Full time/dedicated responsibility for CMC leadership and project management for commercial and pipeline small... .../history and process characterization to management and regulatory agencies. Review submissions through registration of the product...Full timeLocal area
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- ...us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Director I Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients. Prepares CMC...Local area
$200k - $270k
...and follow us on X, LinkedIn and Facebook. Role Summary The Director of Compliance provides compliance guidance on a wide range of... .... The Director works closely with Medical, Commercial, Regulatory Affairs, and G&A colleagues. We seek a strategic, collaborative, solutions...Local area- ...and preparation of document packages for regulatory submissions ensuring compliance with the... ...departments. Participates in assigned Regulatory Affairs initiatives aimed at improving internal... ...experience and understanding of CMC requirements for Small Molecule drugs. Prior...Work at office
- ...matters for patients – realizing a world where people with immune‑mediated diseases can live fully. Job Summary The Executive Director, Regulatory Affairs will report to the Senior Vice President, Regulatory Affairs & Quality and serve as the Global Regulatory Lead to...For contractorsLocal area2 days per week
$116k - $160k
...Job Description We are seeking an experienced regulatory professional to support global regulatory activities across early- and late-stage... ...through lifecycle management. The Manager, Regulatory Affairs will partner cross-functionally to support high-quality regulatory...- ...EMD Serono, Inc. is seeking a Director of Global Labeling to provide strategic regulatory expertise for drug labeling. This role involves overseeing the development... ..., MA. A strong track record in regulatory affairs and excellent communication skills are essential for...3 days per week
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