Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Regulatory Affairs Specialist

Mini Med

MiniMed Career Opportunity

At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world.

About the Role

An individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects – from design to implementation - while adhering to policies, using specialized knowledge and skills normally acquired through advanced education.

Responsibilities may include the following and other duties may be assigned:

  • Prepare, coordinate, and compile regulatory submission packages (e.g., registrations, renewals, design change submissions) to ensure timely approvals in Israel and potential other countries.
  • Lead or support activities required for annual registrations and license renewals.
  • Collaborate with regional post-market and quality teams to ensure compliant execution of vigilance requirements and post-market regulatory obligations.
  • Lead and support activities required for Regulatory Clinical submissions
  • Review promotional materials, labelling, and product claims for regulatory accuracy and compliance.
  • Engage directly with regulatory authorities on defined matters, supporting queries, data requests, and remediation activities.
  • Recommend regulatory strategies to support the earliest possible approval.
  • Monitor regulatory trends and support MiniMed readiness for evolving requirements in Israel.

Required Knowledge and Experience:

  • Bachelor's degree in Life Sciences, Engineering, Chemistry, or related technical field
  • 2-5 years of medical device regulatory experience (depending on level) tied to Israeli submissions and processes, with strong knowledge of Israeli regulation
  • Proficiency in Hebrew and English
  • Experience with Israeli registration processes, technical documentation preparation, interaction with Ministry of Health, as well as product release licensing procedures, post-market surveillance, Field Safety Corrective Actions (FSCA) support, while also possessing expertise in hosting or supporting regulatory audits

MiniMed offers a competitive salary and flexible benefits package.

At MiniMed, we put people first. A commitment to our employees lives at the core of our values: We recognize their contributions. They share in the success they help create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every stage of your career and life.

We want to make every day a better day for people living with diabetes. Our team of creative innovators around the globe share a passion for finding the simplest solutions to the problems that people with diabetes face on a daily basis. For more than 40 years, we've been redefining what's possible, from intelligent dosing systems designed for real life to predictive insights that stay a step ahead, and we're dedicated to continuing to support our customers through every step of their journey — meeting them where and how they need it.

Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Regulatory Affairs Specialist in United States vacancy
  • The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software as a medical device, and... 
    Suggested

    Cedent Consulting

    Plano, TX
    2 days ago
  • Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within the Interventional Cardiology and Vascular Therapies Division. This role is responsible for ensuring compliance with... 
    Suggested

    Katalyst Healthcares & Life Sciences

    Minneapolis, MN
    3 days ago
  •  ...Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S...  ...of international product registrations and related regulatory affairs activities, including execution of procedures and systems... 
    Suggested
    Work at office

    Katalyst Healthcares & Life Sciences

    Irvine, CA
    13 hours ago
  • $120k - $160k

     ...members to perform at a higher level through a deep understanding of their bodies and daily lives.WHOOP is looking for a Regulatory Affairs Specialist II, Expansion to be a core member of the Digital Health team.As the Regulatory Affairs Specialist II, Expansion, you... 
    Suggested
    Full time
    Work at office
    Relocation

    WHOOP

    Boston, MA
    9 hours ago
  •  ...Name: Atrium Medical CorporationJob Location: Merrimack, NH 03054 Employer will allow a hybrid work schedule.Job title: Regulatory Affairs Specialist IIEducation: Bachelor's degree in a scientific or engineering disciplineSOC Code: 13-1041.07SOC Occupation Title: Regulatory... 
    Suggested
    Worldwide
    Flexible hours

    Getinge

    Merrimack, NH
    3 days ago
  • $117k - $120k

    AMNEAL PHARMACEUTICALS Regulatory Affairs Specialist: With minimal supervision assists with the preparation of high-quality regulatory submissions to the Food and Drug Administration (FDA) as required, within company timelines and in accordance with regulatory guidelines... 
    For contractors
    Local area

    Amneal Pharmaceuticals

    Piscataway, NJ
    4 days ago
  • Job Title: Regulatory Affairs SpecialistREMOTEContract: 1 Year and Possibility of ExtensionClient is seeking an experienced Regulatory Affairs contractor to support the preparation and submission of a US FDA 510k and the development of global regulatory documentation,... 
    For contractors

    Integrated Resources

    New York, NY
    2 days ago
  • Job-ID31525652Reference25-04486 ​​​​​ Responsibilities: The Regulatory Affairs Specialist is responsible for working with cross-functional teams to bring IVD (In-Vitro Diagnostic), Research (RUO) and Laboratorial products to market and support activities related to Quality... 

    Katalyst Healthcares & Life Sciences

    Charlotte, NC
    2 days ago
  •  ...financial flexibility by offering contingent labor as a variable cost.Job DescriptionThis individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual... 
    Work at office
    Immediate start

    Artech

    Bridgewater, NJ
    4 days ago
  •  ...approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.A Regulatory Affairs Specialist II position is available in the Diamond Research Laboratory. You will assist and support internal and external PIs, for... 
    Work experience placement

    City of Hope

    Duarte, CA
    3 days ago
  • Overview This is a REMOTE position. The Regulatory Affairs Specialist 2 responsibilities are narrowly focused to a specific country and/or region in which the Specialist has proficient language skills (reading/writing/speaking). This position requires the ability to... 
    H1b
    Work at office
    Local area
    Remote work
    Afternoon shift
    Early shift

    Cook Medical

    Bloomington, IN
    2 days ago
  • The Regulatory Affairs Specialist 3 develops and executes regulatory strategy and integrates regulatory requirements throughout the product lifecycle. Relies on extensive experience and judgment to plan, create, develop and maintain materials needed for regulatory compliance... 

    Cedent Consulting

    Addison, TX
    2 days ago
  •  ...is working in the CMC area. Relevant experience is requiredExperience: 3 to 6 yearsExperience with drug/biologics licensurePrior regulatory experienceTechnical writing experience (CMC experience )Scientific background,Required Skills:CMC/ Regulatory writing experienceScientific... 
    Work at office
    Immediate start

    Artech

    Swiftwater, PA
    2 days ago
  •  ...both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical...  ...Master s Degree a plus• 4+ years of pharmaceutical regulatory affairs experience• Strong knowledge of NDA, ANDA, MAA, BLA, CTA, or... 
    Work at office
    Local area
    Immediate start

    Artech

    Bridgewater, NJ
    2 days ago
  •  ...make a positive impact on consumers, communities, and teammates. Join our team. #CloroxIsThePlaceYour role at Clorox:The Regulatory Affairs Specialist II provides regulatory leadership to support the compliance and safety of Clorox’s FDA-regulated Foods portfolio,... 
    Full time
    Summer work
    Work at office
    Remote work
    Flexible hours
    3 days per week

    The Clorox Company

    Alpharetta, GA
    9 hours ago
  • The Compliance Specialist reports to the Director Legal, Compliance, Privacy & Security (“Director”) and has a key role in supporting the...  ...basis.Conduct research and develop written communication on regulatory requirements to ensure ongoing updates upon request. Manage compliance... 
    Contract work

    Cedent Consulting

    Houston, TX
    2 days ago
  •  ...will not offer sponsorship or take over sponsorship of an employment VISA for this position at this timeAbout the Role The Regulatory Affairs Specialist I supports product development, regulatory submissions, global registrations, and regulatory compliance activities... 
    Hourly pay
    Internship
    Work at office
    Local area
    Shift work
    3 days per week

    Boston Scientific Corporation

    Maple Grove, MN
    1 day ago
  •  ...439Reference25-02134 Responsibilities: Contributes to the FDA regulatory submission process; may aid in authoring and/or publishing electronic...  ...equivalent). A minimum of 3 years' experience in Regulatory Affairs Advanced experience in the areas that may include preparation... 
    Work at office

    Katalyst Healthcares & Life Sciences

    Tampa, FL
    2 days ago
  •  ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the... 
    Immediate start

    Artech

    Cambridge, MA
    2 days ago
  •  ...medical technology or similar. 5+ years of experience in Reg Affairs, QA, R&D, Manufacturing, and/or Project Management within the...  ...verbal and written communication skills. Thorough knowledge of policies, practices and procedures related to Regulatory Affairs.

    Katalyst Healthcares & Life Sciences

    Irvine, CA
    2 days ago
  •  ...Seeking a remote, 12-month contract Global Regulatory Affairs Specialist, the candidate will coordinate and support the maintenance of labeling intelligence, ensuring compliance and alignment with business needs while managing label tracking strategies throughout the product... 
    Contract work
    Local area
    Remote work

    Virtual Vocations Inc

    United States
    4 days ago
  • $70k - $95k

     ...Job Title Industry Regulatory Affairs Job Type FT-Days Location REMOTE OPTION Salary $70,000 - $95,000 Job Description Responsibilities in this position will include: Supports preparation and maintenance of program annual reports, and may support... 
    Contract work
    Work at office
    Remote work

    KMR Search Group

    United States
    1 day ago
  •  ...Smithville is seeking a Staff Accountant to develop expertise in regulatory accounting and reporting while strengthening month-end close and data analysis. This on-site role involves coordination with finance, billing, operations, and external regulatory agencies to ensure... 

    Smithville

    Ellettsville, IN
    6 hours ago
  • $30 - $40 per hour

    Property Services Technician - NH We are seeking a skilled carpenter to serve the northern MA and southern NH/ME market on a fast-paced, Property Services team at an integrated architecture and construction firm. We offer white glove, concierge-quality home maintenance...
    Hourly pay
    Full time
    For subcontractor
    Seasonal work
    Flexible hours

    NH-Jobs.com

    North Hampton, NH
    13 hours ago
  •  ...Work proactively with cross-functional teams to ensure product regulatory compliance and provide necessary regulatory documentation...  .... Requirements: ~1-3 years experience in regulatory affairs field of Laundry and detergents or CPG products. ~ Knowledge... 
    Temporary work
    Work at office
    Local area

    Zobility

    Trumbull, CT
    1 day ago
  •  ...Clinical Regulatory Affairs Specialist I It's More Than a Career, It's a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become... 
    Full time
    Work experience placement
    Local area
    Remote work
    Relocation package

    Sarah Cannon

    United States
    1 day ago
  • $39 - $44 per hour

     ...Remote Regulatory Affairs Specialist Primary Talent Partners has a new contract opening for a Remote Regulatory Affairs Specialist with our healthcare client in Skaneateles, NY. This is a 9-month contract with a potential for extension. Pay: $39.00 - $44.00/hr; W... 
    Contract work
    Local area
    Remote work
    Flexible hours

    Primary Talent Partners

    United States
    22 hours ago
  •  ...To support regulatory and pharmacovigilance activities, the full-time Regulatory Affairs Specialist will manage the preparation of regulatory applications, ensure compliance with local and EU legislation, and provide consultancy to partners while working in Montenegro... 
    Full time
    Local area
    Remote work

    Virtual Vocations Inc

    United States
    1 day ago
  •  ...state statutes and regulations related to pesticide registration (required). Working knowledge of relevant federal and state regulatory programs (e.g., FIFRA, TSCA, Prop 65). (required) Experience in managing multiple complex product registration, safety and compliance... 
    Work at office
    Local area
    Work from home
    3 days per week

    Managed Staffing

    Trumbull, CT
    3 days ago
  •  ...Regulatory Affairs Specialist 4 Primary Function of Position The Sr. Regulatory Affairs primary responsibilities include developing regulatory plans, reviewing design input/output documentation, identification of applicable standards and guidance documents, performing... 

    eTeam

    Sunnyvale, CA
    1 day ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Regulatory Affairs Specialist. Be the first to apply!