Browse Jobs
Browse fresh roles from company career pages, then filter by keyword, location, salary, skills, remote scope, and more. Each listing links back to the employer-controlled apply path when available.
241 jobs match your filters
1mo
L
Regulatory Affairs Specialist
Lsi
Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies, in-depth regulatory know-how, manufacturing and process development help our customers to safeguard nutrition, health and infrastructure efficiently through chemistry and bi
UK-Manchester
onsitePart-time
1mo
A
Regulatory Affairs Specialist
Analogdevices
About Analog Devices Analog Devices, Inc. (NASDAQ: ADI ) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive advancem
Ireland-Limerick
onsiteFull-time
1mo
Regulatory Affairs Specialist
Zimmer Biomet
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team mem
Bogota, Capital District, Colombia
onsite
1mo
L
Regulatory Affairs Specialist
Lonza
Supervisor、薬事・登録担当者 勤務地：東京 ロンザ ジャパンの薬事（Regulatory Affairs）チームに参加し、日本における薬事業務および薬事インテリジェンスをリードする重要な役割を担っていただきます。本ポジションでは、高いパフォーマンスを発揮するチームを導き、社内外のステークホルダーと密接に連携し、日本の規制を遵守しながら革新的なライフサイエンスソリューションを市場に届けることに貢献していただきます。 本ポジションの魅力： 柔軟なキャリア形成とダイナミックな職場環境 多様性を受け入れ、かつ倫理的な職場文化 高い成果を正当に
JP, Tokyo
remoteFull-time
1mo
Regulatory Affairs Specialist
Tempus AI
Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evide
Chicago
hybridFull-time
1mo
Regulatory Affairs Specialist
Enovis
À propos de nous ENOVIS™ Enovis Corporation (NYSE : ENOV) est une entreprise de technologie médicale en forte croissance, centrée sur l’innovation et engagée dans le développement de solutions cliniquement différenciées, visant à améliorer concrètement les résultats pour les pa
Mouguerre, Nouvelle Aquitaine, France
onsiteFull-time
1mo
Regulatory Affairs Specialist
Masimo
Regulatory Affairs Specialist is responsible for obtaining and documenting our mission-critical, Indian regulatory clearances for Masimo’s amazing innovative medical device products. The individual will be the sole RA representative on various project teams for new products or pr
Bengaluru, India
hybrid
1mo
Regulatory Affairs Specialist
Summit Utilities, Inc.
Join our Growing Team and see why Summit Utilities, Inc was named as one of the Fastest Growing Denver Area Private Companies 2019 and 2020; Best Places to Work in Maine 2019, 2020, 2021, 2022 and 2023; and Best Places to Work in Arkansas 2020 and 2023, Oklahoma 2022 and 2023 and
TX, US
hybridFull-Time
2mo
H
Regulatory Affairs Specialist
HP Hood
Are you a self-driven person looking to advance your career as a high-impact player on a team? If so, we have an exciting challenge for you and your future! Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration
Wilmington, MA
onsiteEasy Apply
2mo
L
Regulatory Affairs Specialist
Lonza
Location: Hyderabad, India Join Lonza’s Global Capability Center (GCC) in Hyderabad and play a key role in global regulatory submissions. As a Specialist in Regulatory Affairs (CMC), you will be responsible for site and customer CMC writing actvities for clinical trial applicati
IN Hyderabad
onsiteFull-time
2mo
L
Regulatory Affairs Specialist
LGC Group
We're looking for a meticulous and analytical Regulatory Affairs Specialist to join our team in Milford, United States. This outstanding opportunity at LGC will allow you to be at the forefront of regulatory excellence and conformity, ensuring our organization competes successful
Milford, MA, United States
hybridFull-timeAssociateEasy Apply
2mo
R
Regulatory Affairs Specialist
Roche
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and profess
Tokyo
hybridFull-time
2mo
Regulatory Affairs Specialist
Roche
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and profess
Tokyo, Tokyo, Japan
remoteFull-time
2mo
Regulatory Affairs Specialist
Straumann Group
Position Summary The Regulatory Affairs Specialist is responsible for identifying and obtaining scientific, engineering, and regulatory information for review, preparation, and maintenance of technical documentation for submission to regulatory authorities in the countries/region
Madrid, Spain
hybridFull-time
2mo
Regulatory Affairs Specialist
Pivotal
Pivotal is the leader in the emerging market of electric Vertical Takeoff and Landing (eVTOL) aircraft. We design, develop, and manufacture light eVTOL aircraft and are renowned for the BlackFly aircraft the world's first light eVTOL to fly manned missions and enter the consumer
United States$120K - $150K
remoteFull-timeEasy Apply
3mo
Regulatory affairs specialist
Pierre Fabre Laboratories
Who we are ? The Pierre Fabre Group is unique in France: 2nd Dermo-Cosmetics laboratory in the world and 2nd private French Pharmaceutical group. Our group is 86% owned by the Pierre Fabre Foundation, recognized as being of public utility by the French government and which is de
Mexico - Corporativo Legaria
onsiteFull-time
108mo
I
Regulatory Affairs Specialist
Integrated Resources INC
Regulatory Affairs Specialist position: • Exhibit a competence in US & foreign government regulations regarding the manufacture & distribution of medical devices • Assist with activities necessary for the timely preparation, writing & submitting of international registrations (te
Salt Lake City, UT, United States
hybridContractMid-Senior LevelEasy Apply
108mo
I
Regulatory Affairs Specialist
Integrated Resources INC
Regulatory Affairs Specialist position: • Exhibit a competence in US & foreign government regulations regarding the manufacture & distribution of medical devices • Assist with activities necessary for the timely preparation, writing & submitting of international registrations (te
Salt Lake City, UT, United States
hybridContractMid-Senior LevelEasy Apply
120mo
I
Regulatory Affairs Specialist
Integrated Resources INC
Job Title: Regulatory Affairs Specialist Location: North Haven, CT Duration: 7+ months (Possibility of extension) Job Roles & Responsibilities Compiles all materials required in submissions, license renewal, and annual registration. Technical file remediation, DHF experience, Mic
North Haven, CT, United States
hybridMid-Senior LevelEasy Apply
121mo
I
Regulatory Affairs Specialist
Integrated Resources INC
Job title: Regulatory Affairs Specialist Location: Mansfield, MA Duration: 5+ months (possibility of extension) ROLES& RESPONSIBILITY: · The skills required include a Regulatory Affairs contracted professional with experience working on product development teams, familiar
Mansfield, MA, United States
onsiteMid-Senior LevelEasy Apply
123mo
C
Regulatory Affairs Specialist
Collabera
Role Summary/Purpose: • The Regulatory Affairs Leader - Pharma may be involved in Pre or Postmarket duties or both. • He/she provides subject matter expertise and works with a team of RA professionals to ensure • Establishes best practices in premarket & postmarket for RA, and en
Marlborough, MA, United States
remoteContractMid-Senior LevelEasy Apply
125mo
C
Regulatory Affairs Specialist
Collabera
Regulatory affairs with Technical Files, or equivalent in an R&D or quality position with hands-on experience in the preparation, review, and/or auditing of medical device DHFs, Risk Management files, and/or DMR’s. Must have knowledge of European/International and US regulations
Mansfield, MA, United States
onsiteContractMid-Senior LevelEasy Apply
133mo
I
Regulatory Affairs Specialist
Integrated Resources INC
Role profile: This role will be responsible for co-ordination of global regulatory submissions for in vitro diagnostic devices. Responsibilities will include: • Partnering with global regulatory contacts to understand requirements for product registrations for new and modified pr
Wayne, PA, United States
hybridMid-Senior LevelEasy Apply
11h
Regulatory Affairs Specialist
Novo Nordisk
Are you passionate about ensuring regulatory compliance and navigating the complexities of regulatory frameworks? Do you want to play a key role in gaining approvals for new drugs while safeguarding patient safety? If so, we are looking for a dedicated Regulatory Affairs Speciali
Tashkent, Tashkent, UZ
onsiteToday
1d
Regulatory Affairs Specialist
Novo Nordisk
Are you passionate about ensuring regulatory compliance and navigating the complexities of regulatory frameworks? Do you want to play a key role in gaining approvals for new drugs while safeguarding patient safety? If so, we are looking for a dedicated Regulatory Affairs Speciali
Almaty, Almaty Province, KZ
onsite