International Regulatory Specialist - Medical Devices (Remote)
Chantecaille
Chantecaille’s mission is to create luxurious botanical beauty with impact. For the past 25 years, the brand has been at the cutting-edge of some of the industry’s most exciting innovations in skincare and cosmetics, creating iconic products like Just Skin, Future Skin, Bio Lifting Serum+ and more that are beloved worldwide. Founded by beauty pioneer Sylvie Chantecaille in 1998, the brand is known around the world for its natural-infused skincare and makeup, as well as its' impactful conservation program that supports nonprofits worldwide. Always cruelty-free and PETA-certified, products crafted by Chantecaille are the epitome of forward-thinking and created with a sustainable approach. A Beiersdorf luxury brand, Chantecaille’s global teams include some of the beauty industry’s best-in-class talent, from product formulation to creative direction, marketing and more. The culture of the workplace is collaborative, exciting, and inclusive.
Position Information Ensure compliance and coordinate regulatory product registration globally. Guarantee that our brand Chantecaille meets global relevant cosmetic regulations, with frequent communication between global and local company. Owns portfolio maintenance responsibility, keeping tracking of all regulatory product changes, updating dossiers, artworks, and keeping all countries updated of any registration change. Position Responsibilities Ensures timely and accurate product registration globally Refine and implement registration guidelines, processes and samples preparation Manage, assess, legalize and compile product data for global markets Review documentation for accuracy and compliance with US and international markets Establish synergies and maintain information exchange with third party registration consultants, affiliates, and team members Coordinate formula compliance check and product registration/notification Coordinate the product portfolio maintenance, updating dossiers, artworks and registers Ensures solid procedures according to the cosmetic regulation requirements and product compliance Maintains and optimizes cosmetic system to keep track of all registration, new regulations, and government guidelines Update and maintain Product Information File (PIF) Gives advice to the stakeholders (R&D, Marketing, Legal, Supply Chain and Projects) regarding changes in the registration and impact, informing with clear direction, risk assessment and deadlines Position Qualifications ~ Bachelor’s degree in science or above ~2-3 years of experience in regulatory affairs, Global product registration and notifications in cosmetics, or over-the-counter pharmaceutical industry experience (submissions, operations work a plus) ~ Strong interpersonal and communication skills are also essential to effectively interact with all teams, areas, and levels of business ~ Proactive approach, while being detail and solution oriented, very well organized and having strong analytical skills- Job-ID32758545Reference26-01317Remote50% Remote Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market... ...possess deep knowledge of U.S. and international medical device regulations, strong analytical capabilities...Remote workInternationalMedical device
- ...the full-time Principal Regulatory Affairs Specialist will provide regulatory guidance... ..., author submissions for medical devices, and monitor regulatory... ...changes while working remotely. Key responsibilities... ...premarket submissions and international submissions for medical devices...Remote workInternationalMedical deviceFull time
- ...preparation and submission of regulatory documentation for in vitro diagnostic devices, the full-time remote Regulatory Submission Specialist (EU) will manage the... ...compliance with international regulations, and coordinate... ..., Biomedical Science, Medical Laboratory Science,...Remote workInternationalMedical deviceFull time
$35 - $36 per hour
...Job Title: Regulatory Affairs Specialist Location: Carlsbad, CA Pay Range: $35.00/hr... ...schedule: 3 days on-site / 2 days remote) Duration: 4 months+... ...Affairs experience supporting international markets Strong knowledge of international medical device regulations Ability to work...Remote workInternationalMedical deviceTemporary workShift work- Work Flexibility: RemoteStaff Regulatory Affairs Specialist, Mako and Enabling Technologies (Remote) Join Stryker’s Ortho Tech... ...compliance across U.S. and international markets.Work Flexibility: This... ...requirements for medical devices and related technologies.Author...Remote workInternationalMedical deviceFull timeFor contractors
$95k - $115k
...conditions, is looking for a Sr International Regulatory Affairs Specialist to join its growing Regulatory Affairs... ...Union In Vitro Diagnostic Medical Devices Regulation (IVDR) and Medical Devices... ...ongoing compliance. This is a remote position that will report to the...Remote workInternationalMedical deviceFull timeWork at officeNight shift- ...Regulatory Affairs Specialist – Medical Devices | FDA 510(k) | Quality & ComplianceImmediate need for a talented... ...potential and is located in U.S(Remote).Key Responsibilities:Repare, compile... ...submission packages for U.S. and international regulatory agencies.Support FDA...Remote workInternationalMedical deviceContract work
- ...the largest global medical technology companies... ...Hospital setting. The Regulatory Affairs Specialist I is responsible for... ...domestic and international submissions and other... ...the areas of medical device product registration... ...work-life balance. Remote or field-based positions...Remote workInternationalMedical deviceFull timeWork at officeDay shift
- ...the largest global medical technology companies... ...on site and Friday remotely on a weekly basis in... ...Job DescriptionThe Regulatory Affairs Specialist II is responsible for... ...including domestic and international submissions and... ...and European medical device regulationsMust have...Remote workInternationalMedical deviceFull timeWork at officeDay shift
$90k - $135k
...possible.The Senior Regulatory Affairs Specialist will be an instrumental... ...United States and international markets. This role... ...in vitro diagnostics device company preferred; pharmaceutical... ..., biologics or medical device companies as... ...Compliance (Hybird/Remote) role based in the...Remote workInternationalMedical deviceFull timeWork at officeLocal area- ...Regulatory Affairs Specialist Job Type: Full time - Permanent Location: Madison, New Jersey (On-site... ...of regulatory affairs experience in medical devices or a similar industry ~ Working... ...regulatory processes, plus at least one international market (EU, Canada or Australia) ~...Remote workInternationalMedical devicePermanent employmentFull time
$100k - $105k
...Senior Regulatory Affairs SpecialistLocation... ...Leesburg, VA, or Remote (10% Travel Required... ...family-owned medical technology companies... ...Affairs Specialist in our Regulatory... ...ensure US, EU, and international regulatory requirements... ...regulated medical device industryHands-on...Remote workInternationalMedical deviceWork at office$90k - $135k
...Senior Regulatory Affairs Specialist supporting post-market compliance for in vitro diagnostic products in US and international markets. Responsibilities include adverse event assessment... ...preferred; pharmaceutical, biologics, or medical device acceptable Strong FDA...Remote workInternationalMedical deviceWork at office- ...Regulatory Affairs Specialist II Fully Remote (within US) | Flexible Hours | 40 hr/week If you are a regulatory... ...of experience preparing FDA medical device submissions, and you want your... ...technologies) to appropriate US, EU, and international regulatory pathways and risk...Remote workInternationalMedical deviceFor contractorsWork at officeWorldwideFlexible hours
- ...Senior Regulatory Affairs SpecialistAt BD, we offer an outstanding... ...Senior Regulatory Affairs Specialist to join a world-class team... ...vital for marketing medical devices internationally. This role ensures that product... ...and work-life balance. Remote or field-based positions will...Remote workInternationalMedical deviceWork at officeWorldwide
$90k - $135k
...possible.The Senior Regulatory Affairs Specialist will be an instrumental... ...United States and international markets. This role... ...in vitro diagnostics device company preferred; pharmaceutical... ..., biologics or medical device companies as... ...Compliance (Hybird/Remote) role based in the...Remote workInternationalMedical deviceFull timeWork at officeLocal area$109k - $185k
...Principal Regulatory Affairs SpecialistAt MiniMed, you... ...Regulatory Affairs Specialist at MiniMed, you'll play... ...guiding innovative medical devices and software through... ...the business—US, EU, international regulatory teams as well... ....Position is 100% remote.Ability to travel, up...Remote workInternationalMedical deviceLocal areaFlexible hours$83k - $103.7k
...POSITION SUMMARY: The Sr. Regulatory Affairs Specialist is responsible for the... ...market new or modified medical devices and in vitro diagnostic devices... ...in both domestic and international clinical markets. This... ...labor considerations. Remote USA $83,000—$103,700 USD...Remote workInternationalMedical deviceFull timeWork at officeImmediate startWorldwide- ...Senior International Regulatory Affairs SpecialistBD is one of the largest global medical technology companies in the world... ...Regulatory Affairs Specialist will be responsible... ...submissions of medical devices worldwide.Job... ...work-life balance. Remote or field-based positions...Remote workInternationalMedical deviceWork at officeWorldwide
$124k - $170.5k
...Description: Senior Regulatory Affairs Specialist At Solventum, we... ...compliance throughout the device’s lifecycle. You... ...ISO 13485, Medical Device Single Audit... ...submissions, or other international medical device regulatory... ...Location Work location: Remote (United States)...Remote workInternationalMedical deviceContract workH1bLocal areaWorldwideRelocation packageFlexible hours- ...What Regulatory Affairs contributes to Cardinal... ...pharmaceutical, medical and biotechnology... ...: This is a remote position, and the... ...Regulatory Affairs Specialist supports the Medical... ...requirements for international product... ...regulatory and medical device requirements. Monitor...Remote workInternationalMedical deviceTemporary workWork experience placementLocal areaFlexible hours
$73.76k - $91.2k
...position is intended to provide Regulatory Affairs support to FUJIFILM... ...(U.S. FDA) medical device regulatory requirements, applicable... ...Technical Documentation and International Regulatory Submissions. Evaluate... ...25-1313). Job Locations US-Remote Category Regulatory/...Remote workInternationalMedical deviceLocal areaFlexible hours- ...Masimo is a global medical technology company that... ...possible. The _ Regulatory Affairs Specialist _ is responsible for... ...innovative medical device products. The individual... ...team managing international and domestic filings... ...benefits of flexible, remote working arrangements...Remote workInternationalMedical deviceWork experience placementLocal areaWork from homeFlexible hours
- The Kardion Regulatory Affairs team is seeking a high... ...Principal Regulatory Affairs Specialist is a senior technical... ...III cardiovascular medical devices. In this highly... ...and PMAs—as well as international dossiers such as Technical... ...and two days remote. Physical Abilities:...Remote workInternationalMedical deviceFull timeContract work3 days per week
$140k - $185k
...and most serious unmet medical needs. We work to... ...treatment options, creating devices aimed at restoring... ...Foundry. The Senior Regulatory Specialist will serve as the... ...CE marking, and other international registrations. Drive... ...snacks provided for non‑remote employees Paid...Remote workInternationalMedical deviceFull timeLocal areaFlexible hours$28 - $37 per hour
...is partnering with a top healthcare and medical device organization to identify a Regulatory/Environmental Specialist for a REMOTE opportunity. Responsibilities The role... ...products. The position will work with the international regulatory affairs group to ensure products...Remote workInternationalMedical deviceWork at officeLocal areaFlexible hours$129.6k - $207.4k
...of the largest global medical technology companies in... ...and executing regulatory submissions required to... ...and modified medical devices in the United States, Europe, and other international markets. The role leads... ...and work-life balance. Remote or field-based positions...Remote workInternationalMedical deviceHourly payWork at officeFlexible hoursShift work$64k - $102.35k
...their merit. Job Function: Regulatory Affairs Group Job Sub... ...work. There is no full-time remote option. Key Responsibilities... ...maintenance of existing products, international registrations, and dossiers... ...preferred, preferably with medical devices. Relevant internship...Remote workInternationalMedical deviceFull timeInternshipImmediate startFlexible hours- ...Providing hands-on regulatory support, the contracted entry-level... ...preparation activities in a remote work environment. Key... ...organization of documentation for international regulatory submissions... ...regulatory affairs, quality, medical device, pharmaceutical, or related...Remote workInternationalMedical device
$95k - $110k
...client, a well-established medical device manufacturer in the... ...area, is seeking to hire a Regulatory Affairs Specialist immediately to prepare and... ...with local, national, and international regulations. This role supports... ...a hybrid element with remote work on Fridays, while...Remote workInternationalMedical devicePermanent employmentWork at officeLocal areaImmediate start
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