Current jobs related to Regulatory Affairs Manager III - Cambridge - The Fountain Group


  • Cambridge, Massachusetts, United States Philips Full time

    Job TitleRegulatory Affairs Senior ManagerJob SummaryPhilips is seeking a highly experienced Regulatory Affairs Senior Manager to lead regulatory projects for Philips Clinical Informatics organization. The successful candidate will play a critical role in ensuring and maintaining global accurate regulatory strategy and market access for Philips Disease...


  • Cambridge, Ohio, United States Philips International Full time

    As a Manager of Regulatory Affairs Programs, you will play a pivotal role within the Philips Regulatory Affairs Centralized Services Team, dedicated to enhancing the quality of life for individuals globally.Your Responsibilities:• Oversee and direct the comprehensive strategy and implementation of FDA Establishment Registrations and Listings throughout the...


  • Cambridge, Massachusetts, United States Philips North America Full time

    Job Title: Regulatory Affairs Senior SpecialistJob Description:In light of the pressing challenges our world faces today, the mission of Philips has never been more significant. If you share our commitment to enhancing lives, your contributions will be pivotal in shaping a more equitable future for everyone.In this position, you will have the opportunity...


  • Cambridge, Massachusetts, United States Philips Full time

    Job SummaryWe are seeking a highly experienced and skilled Director of Regulatory Affairs and Quality to lead our Regulatory Affairs and Quality teams in the development and execution of compliant regulatory strategies and quality team/QMS responsibilities.Key ResponsibilitiesRegulatory Affairs Strategy and ExecutionDevelop and execute end-to-end regulatory...


  • Cambridge, United States Catalytic Data Science Full time

    Job DescriptionJob DescriptionSalary: Job Title: Regulatory Affairs Informatics SpecialistLocation: Remote (Quarterly In-Person Team Meetings)Company: Catalytic Data ScienceAbout Us:Catalytic Data Science is a start-up revolutionizing the life sciences industry with cutting-edge AI platforms designed to enhance Regulatory Affairs Intelligence. Our talented...


  • Cambridge, Massachusetts, United States Takeda Full time

    Regulatory Affairs Director, Small MoleculesTakeda is seeking a highly experienced Regulatory Affairs Director, Small Molecules to lead our Global Regulatory Affairs CMC team. As a key member of our team, you will be responsible for overseeing the development and execution of regulatory CMC development and registration strategies.Key Responsibilities:Plan,...


  • Cambridge, United States Thymmune Therapeutics Full time

    Job DescriptionJob DescriptionAbout UsThymmune 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. Building on work from leading labs, Thymmune...


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

    Job Title: Regulatory Affairs SpecialistBeam Therapeutics Inc. is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will play a critical role in ensuring the success of our global regulatory submissions.Key Responsibilities:Prepare and compile documentation packages for global regulatory...


  • Cambridge, Massachusetts, United States The Steely Group Full time

    The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and leads regulatory projects across various development phases. This position demands a strategic regulatory expert who will guide drug development initiatives, leveraging extensive expertise to inform project teams on compliance requirements and...


  • Cambridge, Massachusetts, United States The Steely Group Full time

    The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and leads regulatory projects across various development phases. This position demands a strategic regulatory leader who can effectively guide drug development initiatives by leveraging extensive expertise in regulatory frameworks.Key...


  • Cambridge, Massachusetts, United States The Steely Group Full time

    The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and as a leader in regulatory projects across various development phases. This position is essential for guiding drug development initiatives and leveraging extensive regulatory knowledge to support project teams in navigating complex...


  • cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...


  • cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...


  • Cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...


  • Cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...


  • Cambridge, Massachusetts, United States Apnimed Full time

    {"title": "Senior Director of Regulatory Affairs", "content": "Job SummaryApnimed is seeking a highly experienced Senior Director of Regulatory Affairs to lead the development and execution of regulatory strategies to support the approval and commercialization of our therapies globally.This is a key role in advancing our innovative programs through clinical...


  • Cambridge, Massachusetts, United States Moderna Therapeutics Full time

    About the RoleThe Senior Manager of Medical Writing and Regulatory Affairs is a critical position within our Clinical Development team at Moderna Therapeutics. Reporting directly to the Associate Director, Director of Medical Writing, or Senior Director of Medical Writing, this individual will play a pivotal role in delivering high-quality clinical and...


  • Cambridge, Massachusetts, United States Sarepta Therapeutics Full time

    Job SummarySarepta Therapeutics is seeking a highly experienced Regulatory Strategy Director to lead our regulatory affairs efforts. As a key member of our team, you will be responsible for developing and implementing regulatory strategies that ensure compliance with global regulations and facilitate the approval of our therapeutic programs.Key...


  • Cambridge, Massachusetts, United States Philips Full time

    Job Title: Principal Ultrasound Regulatory Affairs SpecialistThe Principal Regulatory Affairs Specialist will play a pivotal role in developing comprehensive regulatory strategies for complex new devices and post-market changes within Philips' Ultrasound business.Your Key Responsibilities:Lead business-critical new product development projects, ensuring...


  • Cambridge, United States 9627 Corixa Corporation Full time

    At 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 and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong...

Regulatory Affairs Manager III

4 months ago


Cambridge, United States The Fountain Group Full time

The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Manager III for a prominent Pharmaceutical client of ours. This position is Remote. Details for the position are as follows:
 
Job Description:

  • Pay: 75.00-86.54/hr on W2.
  • 6-month assignment to start with potential for extension or conversion.
  • Qualifying candidates should have a bachelor’s degree, 3+ years total experience working in Pharma with at least 3 years of Regulatory CMC experience (manufacturing and testing).
  • Experience delivering CMC content for IND or commercial submission activities.
  • US or Latin American experience is a plus.
  • This role is responsible for Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations, and planning for the CMC aspects of assigned projects/products.
  • Responsibilities include preparation and compilation of submission/documentation for specific projects working as or working with the Regulatory CMC Lead and key stakeholders, primary contact for affiliates on Regulatory CMC activities in the assigned regions and managing of routine and non-routine Health Authority interactions as delegated.
  • Depending on the stage of development and complexity of the program, this role can be a Regulatory CMC Lead for early-stage development programs or working with the Regulatory CMC Lead for late-stage development or commercial programs. The Regulatory CMC Lead is the primary global contact for Regulatory CMC activities, as delegated.
  • Providing strategic and operational Regulatory CMC expertise and support in cross-functional teams, as required, and working flexibly within and across regions to provide broad operational support to ensure the delivery of project/products and business objectives.
  • Successful authoring and contribution to delivering CMC submission documents of development and/or marketed products (biological, oligonucleotide, and/or chemical entities).