Current jobs related to Senior Manager, CMC Regulatory Expert - Cambridge, Massachusetts - Relay Therapeutics


  • Cambridge, Massachusetts, United States Takeda Full time

    About the Role:We are seeking a highly experienced Senior Director, Regulatory Affairs CMC to join our team at Takeda. As a key member of our Regulatory Affairs CMC team, you will be responsible for establishing collaboration with Global CMC teams and leadership through networks and enabling CMC regulatory team's success in meeting goals/objectives.Key...


  • Cambridge, Massachusetts, United States Agios Pharmaceuticals Full time

    Associate Director, Regulatory Affairs - CMCAgios Pharmaceuticals is seeking a highly skilled Associate Director of Regulatory Affairs - CMC to join our Regulatory Affairs team. As a key member of our team, you will be responsible for leading CMC regulatory strategy to support global development and lifecycle management.The Impact You Will MakeYou will be...


  • Cambridge, Massachusetts, United States Takeda Pharmaceutical Full time

    Job DescriptionAt Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on three therapeutic areas and other targeted investments, we push the boundaries of what is possible to bring life-changing therapies to patients worldwide.Key...


  • Cambridge, Massachusetts, United States Takeda Pharmaceutical Full time

    Job OverviewWe are seeking a highly experienced Senior Director and Regulatory Platform Lead to join our team at Takeda Pharmaceutical. This role will be responsible for leading the development and implementation of innovative regulatory strategies for CMC, Device and Drug-Device Combinations Material Sciences.Key ResponsibilitiesDevelop and implement...


  • Cambridge, Massachusetts, United States Biogen Full time

    Job SummaryWe are seeking a highly experienced Regulatory CMC Team Lead to lead our small molecule portfolio. As a key member of our Regulatory CMC team, you will be responsible for the line management of direct reports, defining regulatory CMC strategy, and planning and preparing global CMC regulatory submissions.Key ResponsibilitiesAccountable for line...


  • Cambridge, Massachusetts, United States Agios Pharmaceuticals Full time

    Job Summary:We are seeking a highly motivated and experienced Senior Analytical Development Manager, CMC to join our growing CMC team at Agios Pharmaceuticals. The successful candidate will be responsible for leading the analytical development function within CMC and contributing to the overall CMC strategy of drug development at Agios.Key Responsibilities:...


  • Cambridge, Massachusetts, United States Takeda Pharmaceutical Full time

    Job DescriptionTakeda is seeking a Senior Director and Regulatory Platform Lead for CMC, Device and Drug-Device Combinations Material Sciences to join our team. As a key member of our regulatory team, you will be responsible for developing and implementing innovative regulatory strategies for pure device and combination product submissions, with a focus on...


  • Cambridge, Massachusetts, United States Takeda Pharmaceutical Full time

    Job DescriptionTakeda Pharmaceutical is seeking a highly skilled and experienced Senior Director and Regulatory Platform Lead to join our team. As a key member of our regulatory affairs team, you will be responsible for leading the development and implementation of innovative regulatory strategies for CMC and device-drug combinations.Key...


  • Cambridge, Massachusetts, United States Takeda Pharmaceutical Full time

    Job DescriptionTakeda is seeking a highly experienced Senior Director and Regulatory Platform Lead to join our team in Cambridge, MA. As a key member of our Regulatory Affairs department, you will be responsible for leading the development and implementation of innovative regulatory strategies for device and combination products.Key Responsibilities:Develop...


  • Cambridge, Massachusetts, United States Takeda Pharmaceutical Full time

    Job DescriptionTakeda Pharmaceutical is seeking a highly skilled and experienced Senior Director and Regulatory Platform Lead GRA CMC, Device and Drug-Device Combinations Material Sciences to join our team. As a key member of our regulatory affairs team, you will be responsible for leading the development and implementation of innovative regulatory...


  • Cambridge, Massachusetts, United States Agios Pharmaceuticals Full time

    Role SummaryAgios Pharmaceuticals is seeking a highly motivated Associate Director, Analytical Development, CMC to join our growing CMC team. The ideal candidate will be a key stakeholder within analytical development team to help build and lead the analytical development function within CMC and hands-on contributor to the overall CMC strategy of drug...


  • Cambridge, Massachusetts, United States PSG Global Solutions Careers Full time

    Associate Director Regulatory Affairs CMC Job DescriptionWe are seeking an experienced Associate Director Regulatory Affairs CMC to join our team at PSG Global Solutions Careers. As a key member of our regulatory affairs team, you will be responsible for developing and executing global regulatory CMC strategies for assigned programs.Key Responsibilities:Lead...


  • Cambridge, Massachusetts, United States BlueRock Therapeutics Full time

    About BlueRock TherapeuticsBlueRock Therapeutics is a leading engineered cell therapy company using its unique cell+gene platform to direct cellular differentiation and genetically engineer cells to create a new generation of cellular medicines that address large patient populations suffering from neurological, cardiovascular, and immunology diseases.Job...


  • Cambridge, Massachusetts, United States Agios Pharmaceuticals Full time

    About the RoleAgios Pharmaceuticals is seeking a highly motivated and experienced Associate Director, Analytical Development, CMC to join our growing CMC team. As a key stakeholder within analytical development, you will be responsible for building and leading the analytical development function within CMC and contributing to the overall CMC strategy of drug...


  • Cambridge, Massachusetts, United States Voyager Therapeutics, Inc. Full time

    Job Title: Associate Director, Regulatory Affairs CMCVoyager Therapeutics, Inc. is seeking an experienced Associate Director to lead our Regulatory Affairs CMC team. As a key member of our Regulatory Affairs department, you will be responsible for developing and implementing global Regulatory CMC strategies to secure approval of our gene therapy products.Key...


  • Cambridge, Massachusetts, United States Apex Systems Full time

    Job Title: Senior Director, Cell Therapy CMC/Process DevelopmentApex Systems is seeking a highly experienced Senior Director to lead process development, process scale-up, optimization, and technical transfer of Cell Therapy Products. This role will work closely with Contract Development and Manufacturing Organizations (CDMOs) for process development and...


  • Cambridge, Massachusetts, United States Takeda Full time

    Job SummaryTakeda is seeking a highly experienced Senior Director and Regulatory Platform Lead to join our team. As a key member of our regulatory team, you will be responsible for developing and implementing innovative regulatory strategies for device and combination product submissions.Key ResponsibilitiesDevelop and implement global regulatory strategies...


  • Cambridge, Massachusetts, United States Korro Bio, Inc. Full time

    About Korro Bio, Inc.Korro Bio, Inc. is a biopharmaceutical company pioneering the development of genetic medicines for rare and prevalent diseases using its proprietary RNA editing platform. Our mission is to harness the body's natural RNA editing process to deliver precise and transient single base edits, expanding the reach of genetic medicines and...


  • Cambridge, Massachusetts, United States Stratacuity Full time

    Job Overview: We are seeking a highly experienced Senior Director to lead our Cell Therapy Process Development and CMC efforts. This individual will be responsible for developing innovative, scalable expansion and differentiation processes to manufacture cell therapy products.Key Responsibilities:Provide strategic and technical CMC leadership for process...


  • Cambridge, Massachusetts, United States Thymmune Therapeutics Full time

    Job OverviewThymmune Therapeutics is a preclinical biotechnology company based in Cambridge, MA, applying proprietary insights in thymic engineering to develop and commercialize immune cell therapy products addressing significant opportunities with unmet clinical need across immunology.We are seeking a highly skilled and experienced Head of Regulatory...

Senior Manager, CMC Regulatory Expert

2 months ago


Cambridge, Massachusetts, United States Relay Therapeutics Full time
The Opportunity

We are seeking a highly skilled Senior Manager, CMC Regulatory to join our Pharmaceutical Development team. As a key member of our team, you will play a critical role in regulatory strategy development and execution of assigned Chemistry, Manufacturing and Control (CMC) programs.

Your Role
  • Develop and execute CMC global submission plans and timelines in accordance with project goals.
  • Lead the preparation, review, and on-time submission of CMC sections for IND/IMPD/CTA, NDA/MAA and other global regulatory filings.
  • Coordinate responses to CMC questions/RFIs from regulatory authorities in conjunction with CMC and regulatory affairs teams.
  • Lead CMC-regulatory activities with cross-functional teams and act as the regulatory CMC liaison between CMC, regulatory affairs and/or program management.
  • Lead and manage regulatory assessment and guidance on product compliance topics, including change controls, deviations, and GMP investigations.
Competencies for Success
  • Strong background in Regulatory Affairs-CMC with a focus on small molecule clinical (IND/IMPD) and/or commercial (NDA/MAA) submissions.
  • Proven ability to lead and manage regulatory CMC projects.
  • In-depth knowledge of global CMC regulatory requirements and guidelines (e.g. FDA, EMA, ICH).
  • Positive attitude, energetic and proactive.
  • Strong technical writing and document review skills.
Your Background
  • Bachelor or advanced degree in Pharmaceutical Sciences, Chemistry or related fields.
  • Minimum of 6-8+ years of relevant experience in regulatory-CMC or within CMC function (e.g. analytical, formulation and process development, QA, QC) in the biotech/pharmaceutical industry with a focus on CMC for small molecules.
  • Experience with authoring/review/providing CMC content for CMC/quality submissions including IND and IMPD development/maintenance.
  • Knowledge of eCTD Module 3 and QOS requirements for INDs/IMPDs and NDAs/MAAs.
About Relay Therapeutics

Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients.

Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology.

Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets.

We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.

Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you're excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us.