Associate Director, CMC Regulatory Affairs
$166.4k - $249.6kVertex Pharmaceuticals
Job DescriptionGeneral Summary:The Chemistry Manufacturing Controls Associate Director executes multi-product global regulatory CMC strategies for investigational and marketed products. This role leads the preparation and filing of regulatory CMC submissions and manages the interactions with Health Authorities for CMC topics. This role also provides regulatory guidance to various cross-functional teams and ensures all applicable global regulatory requirements are considered and appropriately incorporated into investigational and commercial products. This role may supervise other regulatory staff.Key Duties and Responsibilities:Leads the preparation and review of CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agenciesDevelops global CMC regulatory strategies for one or more investigational and/or marketed productsLeads regulatory colleagues in development of global CMC regulatory strategies and submissionsProvides CMC regulatory guidance to cross-functional teams and key stakeholdersManages regulatory assessment and guidance on product compliance topics including change controls, deviations, and GMP investigationsLeads projects with cross-functional teams and acts as the primary regulatory CMC contact for assigned products and projectsParticipates in the design, development and implementation of department strategies, providing recommendations in area of expertiseKnowledge and Skills:Excellent interpersonal skills to communicate difficult concepts and persuade othersStrategic thinking and strong problem solving skillsCollaborates and communicates in an open, clear, complete, timely, and consistent mannerStrong sense of planning and prioritization, and the ability to work with all levels of managementAdvanced knowledge in regulatory (FDA, EMA, Health Canada and ICH) guidelinesEducation and Experience:Bachelor's Degree in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another life-science fieldTypically requires 8 years of experience in the pharmaceutical or biotech industry or in a related field, or the equivalent combination of education and experienceAt Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.Pay Range:$166,400 - $249,600Disclosure Statement:The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.Flex Designation:Hybrid-Eligible Or On-Site EligibleFlex Eligibility Status:In this Hybrid-Eligible role, you can choose to be designated as: 1. Hybrid: work remotely up to two days per week; or select2. On-Site: work five days per week on-site with ad hoc flexibility.Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time. #LI-HybridCompany InformationVertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at View email address on click.appcast.io: Boston, MAType: Full time
$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 wageLocal areaRemote workWorldwide$170.9k - $231.3k
OverviewThe Associate Director, Regulatory Affairs CMC Development is responsible for developing and implementing 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$166.4k - $249.6k
...Summary: The Chemistry Manufacturing Controls Associate Director executes multi-product global regulatory CMC strategies for investigational and marketed products... ...in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another...SuggestedSummer workRemote workFlexible hours2 days per week- ## Associate Director, Regulatory Affairs CMCApplyremote type: Site Basedlocations: South Boston, MAtime type: Full timeposted on: Posted Todayjob requisition... ...multiple novel therapies to patients. As the Regulatory CMC lead for these programs, you will have the opportunity...SuggestedContract workRemote work
- ...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...SuggestedWorldwide
$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...- Takeda's Global Regulatory Affairs - CMC team in Cambridge, MA is seeking a Regulatory CMC professional to lead regulatory submissions for investigational, registration and post-approval programs across global markets. With minimal supervision, you will define CMC content...
$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$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$147.5k - $221.3k
...Vertex Pharmaceuticals seeks an Associate Director to lead inspection readiness and compliance programs... ...continuous improvement, and ensure regulatory readiness through audits, assessments,... ...health field ~8+ years of relevant CMC quality or compliance experience ~ Knowledge...- Associate Director - Regulatory Affairs CMC Location: Natick, MA About the role: This role provides strategic, tactical and operational regulatory CMC leadership to support clinical trial applications, market registrations and post-approval submissions, along with managing...
$142.5k - $256.5k
The RoleModerna is looking for an Associate Director, Global Regulatory Affairs, CMC, to join our team. This pivotal role will focus on preparing and overseeing CMC and Quality related agency correspondence and regulatory applications, governing CMC submissions, and providing...Permanent employmentFull timeWork at officeWork from home- 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...
$142.5k - $256.5k
...The Role Moderna is looking for an Associate Director, Global Regulatory Affairs, CMC, to join our team. This pivotal role will focus on preparing and overseeing CMC and Quality related agency correspondence and regulatory applications, governing CMC submissions, and...Permanent employmentWork at officeLocal areaWork from home- Anagram Therapeutics, Inc. in Natick, MA is seeking an experienced Associate Director to lead Regulatory Affairs CMC across development and lifecycle stages. You will plan submission strategies, prepare CMC documents for INDs/NDAs/BLAs, and collaborate with cross-functional...
$166.4k - $249.6k
...Vertex Pharmaceuticals seeks an Associate Director in CMC Regulatory Affairs to lead global regulatory strategies for investigational and marketed products. The role involves preparing and filing regulatory submissions, managing health authority interactions, and providing...$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...$241k - $332k
About This Role:As the Head of Regulatory CMC - Biologics & Advanced Therapy Medicinal Products (ATMP), you will lead a dynamic team within... ...regulatory agencies.Active engagement in major industry associations, conferences and forums.Strong collaboration and negotiation...Full timeTemporary workLocal area$161.5k - $218.5k
OverviewThe Associate Director, Downstream, Emerging Modalities, is expected to provide technical... ...Proof Of Concept transition by leading CMC team as necessary for the assigned program... ...Development, Formulation Development, Regulatory, Technical Operations, Quality, and...Full timeTemporary workLocal areaFlexible hours$172.2k - $233k
Overview:Alnylam is seeking an experienced leader to serve as Associate Director, CMC Technology Delivery to lead the digital enablement and... ...products from declaration of Development Candidate (DC) to regulatory filings for Investigational New Drug (IND) and New Drug...Full timeContract workTemporary workLocal areaFlexible hours3 days per week$258.83k - $293.48k
...delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can... ...talent, at the right time, in the right way. The Senior Director of Regulatory Affairs CMC provides highly strategic, tactical and operational...Minimum wageFull timeWork at officeLocal areaFlexible hours3 days per week$177k - $278.08k
...investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. The Director Regulatory Site CMC ensures efficient and compliant management of regulatory change control and post-approval activities at the site level....Minimum wageFull timeLocal areaRemote workWorldwide$230k - $260k
...alternative application process. Director, Regulatory CMC .25 Charlestown-HQ, Charlestown, MA... ...Solid within industry consortia, trade associations, and gene therapy working groups.... ...scientific degree. ~12+ years of Regulatory Affairs experience with significant...Temporary workFlexible hours$175.5k - $283.8k
...Headquartered in Boston, Massachusetts, Centessa was recognized as a Great Place to Work® in 2026. Overview As the Senior Director, Regulatory CMC, you will provide strategic and operational leadership for Regulatory CMC activities across the company's small molecule...Full timeRemote workFlexible hours- ...Relay Therapeutics seeks an experienced CMC regulatory professional to lead chemistry, manufacturing, and control strategy development and... ...and management Requirements ~8-10+ years CMC-regulatory affairs experience, preferably solid oral small molecules ~...
$180k - $205k
...visit . The Role We are seeking a strategic, hands-on Associate Director, Regulatory Affairs to lead regulatory project teams and submission activities... ...to internal teams across clinical, nonclinical, CMC, and commercial functions. Serve as the primary regulatory...Work at office$154k - $215k
...treatments to patients. Learn more: Position Summary The Associate Director, Regulatory Affairs will serve as a regulatory strategist supporting one or... ...& Regulatory Intelligence Partner with Clinical, CMC, Quality, Research, and Commercial teams to ensure regulatory...Local areaRemote workVisa sponsorshipWork visa- Xenon Pharmaceuticals is seeking an Associate Director, CMC, Drug Substance to join the CMC Drug Substance team in Boston, MA. The role focuses... ...programs with CDMOs to support clinical trials and regulatory submissions. The position reports to the Senior Director,...Remote work
- ...includes a second FOS study, X-TOLE3, which would support regulatory submissions outside the U.S., and the X-ACKT study in primary... ...operations. _ About the Role: _ We are seeking an Associate Director, CMC, Drug Substance to join our CMC Drug Substance team. The candidate...Contract workTemporary workRemote workFlexible hours
- Moderna is seeking an Associate Director, Global Regulatory Affairs, CMC, to lead and oversee regulatory activities for CMC and Quality, coordinating worldwide submissions and agency communications. The role requires 10+ years in pharma/biotech with strong EU/ROW regulatory...Work at officeWorldwide
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