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 Madrigalpharma
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Director, Regulatory Affairs CMC in Waltham, MA vacancy
$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$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
...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...SuggestedMinimum 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...SuggestedFull timeSummer workRemote workFlexible hours2 days per week$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...Suggested$210k - $320k
..., and a vision of providing life-long cures to patients suffering from serious diseases.Position Overview: The Regulatory Director/Sr. Director Regulatory CMC will be responsible for preparing CMC and Quality related health authority agency correspondence and regulatory...Full timeShift work3 days per week1 day per week- ## 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
- 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...
$294k - $318k
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$143k - $233k
...team, this position will play a key role in regulatory strategy development and execution of... ...assigned Chemistry, Manufacturing and Control (CMC) programs. Your Role: With minimal... ...authorities in conjunction with CMC and regulatory affairs leads/SMEs.Independently defines CMC...$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$195k - $330k
...ll make an impact:Act as the global regulatory strategy lead for Kymera’s IRF5... ...team, working closely with Clinical, CMC, Nonclinical, Quality, and Commercial... ...degree preferred but not required.Director: 8-10 years of Regulatory Affairs experience. Senior Director: 10-12+...Flexible 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 regulatory...Work at office$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- Relay Therapeutics is recruiting for an Associate Director/Director, CMC Regulatory in Cambridge, MA. You will lead regulatory CMC strategies for small molecule programs, develop global submission plans, and coordinate cross-functional teams to ensure regulatory success...
$210k - $245k
...therapies designed to selectively expand regulatory T cells and reset the immune system.... ...Medicines is seeking an experienced Director of Regulatory Affairs to serve as the company’s first... ...Clinical Development, Clinical Operations, CMC, Quality, and external regulatory...Temporary workWork experience placementWork at officeFlexible hours3 days per week- Beam Therapeutics is seeking a Regulatory Director/Sr. Director Regulatory CMC to lead global regulatory CMC submissions and ensure compliant health authority communications. The role sits within Regulatory and partners with cross-functional teams to shape strategies for...3 days per week1 day per week
$181k - $213k
...information, visit Position Purpose: The Regulatory CMC Senior Manager is responsible for... .... This position will report to the Director of Regulatory CMC. Key Responsibilities... ...relationships within the Regulatory Affairs department and Technical Operations (...Full timeTemporary workRemote work$147.5k - $221.3k
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$184.6k - $277k
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- ...AnnuallyIndustry PharmaceuticalsSelling Points Lead impactful regulatory projects ensuring compliance with FDA standards.... ...flexibility and growth opportunities.Job DescriptionAssociate Director of Regulatory Affairs OverviewThe Associate Director of Regulatory Affairs will...Work at office
$138.75k - $231.25k
Associate Director Regulatory Affairs, OncologyAt GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent...Full timeLocal area$195k - $330k
...make an impact:Drive end-to-end CMC program management for mid to... ..., analytical, quality, regulatory, and supply chain workstreams... ...partnership with Regulatory Affairs and subject matter experts.Serve... ...M.S.) of CMC experience; Sr. Director level requires commensurate additional...$220k - $370k
...team is seeking a highly motivated and experienced Senior Director or VP of Regulatory Affairs. The ideal candidate will have a proven track record of... ...are integrated into clinical, nonclinical, CMC, quality, pharmacovigilance, medical affairs, and commercial...Summer workWork at officeFlexible hours$180k - $245k
...Rosa Therapeutics is seeking an experienced and strategic Director of Regulatory Affairs to lead and support global regulatory efforts across our development... ...is required, and immunology background is preferred. CMC experience is a plus.ResponsibilitiesDevelop and lead...- ...OfficerPosition SummaryThis individual will lead regulatory strategy and execution for growing... ...Development, Clinical Operations, CMC, Quality, and external regulatory partners... ...independently, and help build Regulatory Affairs capabilities as the clinical pipeline grows...2 days per week3 days per week
$215k - $235k
...this sounds like you then please read on!About the Role: The Director of Regulatory Affairs is responsible for leading regulatory strategy and... ...mitigation strategies aligned with clinical, nonclinical, and CMC development plans.Provide regulatory input into development...$218.06k - $327.09k
Job Title: Senior Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Gaithersburg, MDBoston, MASouth San Francisco, CASanta... ...presentations and aligning regulatory objectives with clinical, CMC, safety and commercial strategies.Evidence and Decision-...Hourly payFull timeTemporary workStart working todayWork at officeFlexible hours3 days per week- ...Initiatives role will develop & advocate strategic positions for CMC regulatory/CMC issues with cross functional internal stakeholders and on... ...experience with at least 8-plus years in regulatory affairs and 5-plus years demonstrated enterprise leadership (as described...Full timeLocal 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
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Director, Regulatory Affairs CMC. Be the first to apply!
Related searches
- director global regulatory affairs Waltham, MA
- compliance manager Waltham, MA
- manager regulatory affairs Waltham, MA
- regulatory manager Waltham, MA
- head compliance Waltham, MA
- regulatory affairs director Waltham, MA
- regulatory affairs manager pharmaceutical Waltham, MA
- regulatory & compliance manager Waltham, MA
- compliance director Waltham, MA
- regulatory scientist Waltham, MA

