Current jobs related to Regulatory Affairs Associate - Boston MA - Venus Aesthetic Intelligence


  • Boston, Massachusetts, United States Venus Aesthetic Intelligence Full time

    Title: Regulatory Affairs Associate Reporting to: Regulatory Affairs Manager Location: Boston, Massachusetts, USA We are seeking a highly motivated and results-driven Regulatory Affairs Associate to join our dynamic sales team at Venus AI. You are responsible for supporting global registrations and ensuring that medical devices produced by Venus...


  • Boston, Massachusetts, United States Venus Aesthetic Intelligence Full time

    Title: Regulatory Affairs Associate Reporting to: Regulatory Affairs Manager Location: Boston, Massachusetts, USA We are seeking a highly motivated and results-driven Regulatory Affairs Associate to join our dynamic sales team at Venus AI. You are responsible for supporting global registrations and ensuring that medical devices produced by Venus...


  • Boston, Massachusetts, United States Monte Rosa Therapeutics, Inc Full time

    OverviewMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of Regulatory Affairs. This role will focus on oncology, immunology, and related therapeutic areas. The successful candidate will be responsible for developing and implementing regulatory strategies to support the...


  • Boston, Massachusetts, United States Monte Rosa Therapeutics, Inc Full time

    OverviewMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of Regulatory Affairs. This role will focus on oncology, immunology, and related therapeutic areas. The successful candidate will be responsible for developing and implementing regulatory strategies to support the...


  • Boston, Massachusetts, United States Monte Rosa Therapeutics, Inc Full time

    OverviewMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of Regulatory Affairs. This role will focus on oncology, immunology, and related therapeutic areas. The successful candidate will be responsible for developing and implementing regulatory strategies to support the...


  • Boston, Massachusetts, United States Biolink360 Full time

    Biolink360 seeks a seasoned Regulatory Affairs Director to lead our global pharmacovigilance efforts. The ideal candidate will have 12+ years of experience in regulatory affairs/pharmacovigilance and a strong background in developing regulatory strategies for new product development and registration.The successful candidate will oversee the management of our...


  • Boston, Massachusetts, United States Phia LLC Full time

    At Phia LLC, we are seeking a talented Regulatory Affairs Director to join our team. This role will be responsible for providing strategic regulatory guidance for Companion Diagnostics collaborations with BioPharma partners.The ideal candidate will have 10+ years of Regulatory Affairs experience in the pharmaceutical or diagnostics industry, including 5+...


  • Boston, Massachusetts, United States Planet Interactive Full time

    Associate Director, Regulatory Affairs - Advertising and PromotionsPlanet Interactive is seeking a remote Associate Director, Regulatory Affairs - Advertising and Promotions to join our client that is a global biotechnology company focused on developing and commercializing transformative therapies for people with serious diseases.Pay: $100-$120/hr depending...


  • Boston, Massachusetts, United States Phia LLC Full time

    Our Story\SOPHiA GENETICS is a pioneer in the field of Data-Driven Medicine, driven by a passion to revolutionize healthcare through innovative technology and collaborative partnerships. As a leading provider of AI-powered diagnostic solutions, we are committed to empowering clinicians, researchers, and patients worldwide.\Your Mission\As our next Regulatory...


  • Boston, Massachusetts, United States Jobleads-US Full time

    Job DescriptionAs a seasoned professional in regulatory affairs, you will be responsible for driving regulatory excellence across our organization. This role requires expertise in Companion Diagnostics, Clinical Trial Assays, and associated BioPharma programs. A background in regulatory frameworks within Oncology or Rare Diseases is highly valuable.**Key...


  • Boston, Massachusetts, United States Monte Rosa Therapeutics Full time

    Associate Director / Director, Regulatory Strategy - CMCLocation:Monte Rosa Therapeutics is a clinical-stage biotechnology company seeking a highly skilled and self-motivated regulatory professional to join our team. This role will focus on oncology, immunology, and related therapeutic areas.Key Responsibilities:The Associate Director of regulatory Affairs...


  • Boston, Massachusetts, United States Venus Aesthetic Intelligence Full time

    Title: Regulatory Affairs Associate Reporting to: Regulatory Affairs Manager We are seeking a highly motivated and results-driven Regulatory Affairs Associate to join our dynamic sales team at Venus AI. You are responsible for supporting global registrations and ensuring that medical devices produced by Venus Concept meet all regulatory requirements for...


  • Boston, Massachusetts, United States Takeda Pharmaceutical Full time

    About This OpportunityWe are excited to offer a challenging and rewarding role as Associate Director, Global Labeling Lead at Takeda Pharmaceutical. In this position, you will be responsible for managing labeling projects, collaborating with cross-functional teams, and ensuring regulatory compliance.Key AccountabilitiesProject Management: Manage labeling...


  • Boston, Massachusetts, United States Jobleads-US Full time

    Job Description:Prime Medicine is a leading biotechnology company dedicated to creating and delivering gene editing therapies. The Company utilizes its proprietary Prime Editing platform, a versatile and precise technology, to develop potentially curative genetic therapies.The Regulatory Affairs team is responsible for ensuring compliance with relevant...


  • Boston, Massachusetts, United States Jobleads-US Full time

    Job OverviewWe are seeking a highly skilled Regulatory Affairs Director to join our Quality and Regulatory Affairs team at Withings. This role will be responsible for providing management and leadership to the Regulatory Affairs organization in the development and implementation of regulatory strategies and processes to gain product approvals in the US...


  • Boston, Massachusetts, United States Takeda Full time

    Description Takeda Development Center Americas, Inc. is seeking an Associate Director, Global Regulatory Affairs in Cambridge, MA with the following requirements: Master's degree in Pharmacy, Biomedical Engineering, Regulatory affairs or related field plus 7 years of related experience. Prior experience must include: In the immunology and inflammation...


  • Boston, Massachusetts, United States Planet Interactive Full time

    Planet Interactive seeks a skilled Associate Director, Regulatory Affairs - Advertising and Promotions to join our client, a global biotechnology company focused on transformative therapies for people with serious diseases.We are looking for a professional with specialized knowledge of regulations and requirements governing product promotion and related...


  • Boston, Massachusetts, United States Phia LLC Full time

    About Us\SOPHiA GENETICS, a global leader in Data-Driven Medicine, is seeking a highly skilled and experienced Regulatory Affairs Director to join our team. Our mission is to empower clinicians, researchers, and patients with AI-powered diagnostic solutions that improve health outcomes globally.\Your Impact\As a key member of our regulatory affairs team, you...


  • Boston, Massachusetts, United States Monte Rosa Therapeutics Full time

    Job OverviewMonte Rosa Therapeutics is a clinical-stage biotechnology company seeking an experienced regulatory professional to join our teams. The successful candidate will be responsible for developing and implementing regulatory strategies to support the global development and approval of our innovative therapies.About the RoleThis role will focus on...


  • Boston, Massachusetts, United States Monte Rosa Therapeutics, Inc Full time

    Monte Rosa Therapeutics, Inc. is a leader in the development of innovative therapies. We are seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of Regulatory Affairs.About the RoleThis role will focus on oncology, immunology, and related therapeutic areas. The successful candidate will be responsible...

Regulatory Affairs Associate

4 weeks ago


Boston MA, United States Venus Aesthetic Intelligence Full time

Title: Regulatory Affairs Associate

Reporting to: Regulatory Affairs Manager

Location: Boston, Massachusetts, USA

We are seeking a highly motivated and results-driven Regulatory Affairs Associate to join our dynamic sales team at Venus AI. You are responsible for supporting global registrations and ensuring that medical devices produced by Venus Concept meet all regulatory requirements for countries where the devices are marketed. This role is responsible for executing regulatory strategies, preparing and submitting regulatory documents, and providing guidance and support to cross-functional teams on regulatory matters related to global markets.

Responsibilities:

  • Execute regulatory strategies to support the registration and commercialization of medical devices in compliance with global regulatory requirements.
  • Prepare and submit regulatory documents, including technical files, design dossiers, and other regulatory filings as required for countries outside the United States.
  • Coordinate with in-country regulatory partners and consultants to ensure that all local regulatory requirements are met and all registrations are maintained in good standing.
  • Provide guidance and support to cross-functional teams on regulatory matters related to global markets.
  • Stay up-to-date with changes in global regulatory requirements and industry standards, and communicate these changes to the organization.
  • Ensure that all regulatory submissions are of high quality, complete, and timely.
  • Maintain knowledge of international regulations, standards, and guidance documents and apply that knowledge to global regulatory strategies and submissions.

Qualifications:

  • Bachelor's degree in a scientific or technical discipline.
  • 0-1 years of experience in regulatory affairs, with a focus on global medical device registrations.
  • Knowledge of global regulations and standards for medical devices.
  • Excellent organization and attention to detail
  • Ability to work accurately in a fast-paced ever-changing environment.
  • Ability to work remote
  • Excellent communication and interpersonal skills.

Compensation:

  • Base salary range: $80,000 - $90,000
  • Benefits: Comprehensive package starting on Day 1, covering medical, dental, vision, life insurance, and a 401(k) match, among other benefits.

What you will be part of – our Venus Culture

Venus believes in pushing boundaries while embracing creativity and innovation. Our employees are a critical part of our company’s performance and are at the core of its success. At Venus, we rely on our employees, customers, and network of industry professionals around the world to continuously improve and Deliver the Promise. In order to do that, we ensure that everyone operates with the same values and vision. At Venus, we promise to give you Endless Opportunities, allow you to Foster Innovation and be part of Delivering a Best-In-Class Offering.

Venus is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals. Venus is committed to accommodating persons with disabilities. Accommodation is available on request for qualified candidates during each stage of the recruitment process.

About Venus Concept

Venus Concept is an innovative global medical aesthetic technology leader with a broad product portfolio of minimally invasive and non-invasive medical aesthetic and hair restoration technologies and reach in over 60 countries and 10 direct markets. Venus Concept's product portfolio consists of aesthetic device platforms, including Venus Versa, Venus Versa Pro, Venus Legacy, Venus Velocity, Venus Viva, Venus Glow, Venus Bliss, Venus Bliss MAX, Venus Epileve, Venus Viva MD and AI.ME. Venus Concept's hair restoration systems include NeoGraft® and the ARTAS iX® Robotic Hair Restoration system. Venus Concept has been backed by leading healthcare industry growth equity investors, including EW Healthcare Partners (formerly Essex Woodlands), HealthQuest Capital, Longitude Capital Management, Aperture Venture Partners, and Masters Special Situations.