Job DescriptionSeeking a Product Regulatory Manager for a highly-visible opportunity to lead product regulatory compliance for a global industrial product portfolio while improving the systems, data, and processes that support the function.
This person leads the team and day-to-day regulatory program, ensures compliance across domestic and international markets, evaluates emerging requirements, imp...
Job DescriptionPosition Overview
An established organization operating in a regulated product environment is seeking a Regulatory Affairs Specialist to support regulatory compliance, quality management systems, product registrations, and international market access.
This role will work cross-functionally with quality, engineering, product development, and other internal stakeholders to ensure prod...
Job Description
About the Company
Breckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our products are developed in the group’s own R&D facilities and through strategic partnerships with manufactures from around the world.
About the Role
The Regulatory Affairs Manager is responsible for supporting the development and e...
Job DescriptionChantecaille’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, ...
Our client, a global healthcare organization is seeking a Regulatory Affairs Specialist to join their team. As a Regulatory Affairs Specialist, you will be part of the Regulatory Affairs team supporting division-level regulatory operations. The ideal candidate will have strong attention to detail, the ability to think critically about regulatory requirements, and the discipline to manage deadlines ...
Job DescriptionRegulatory Affairs Specialist, Oncology Clinical Research
*5-6 Month Contract*
Join a leading oncology clinical research organization known for connecting patients with cutting edge cancer treatments and advancing new therapies through clinical trials.
In this role, you will prepare and submit study documents to the IRB for assigned investigational drug studies, including protoc...
Job DescriptionRegulatory Affairs Specialist
Job Type: Full time - Permanent
Location: Madison, New Jersey (On-site)
A commercial-stage transplant technology company, part of a global medtech group, is changing how donor organs are preserved and assessed before transplant. Their flagship platform is already used in thousands of procedures across the US, Europe, Canada and Australia, and they are g...
Job DescriptionGlobal Labeling Strategy Lead (Contract)
Global Pharmaceutical Company
? EST timezone (remote) - US-based
? Full-time | 6‑month contract
? Competitive hourly rate
? Start: ASAP
The Opportunity
A global pharmaceutical organisation is seeking an experienced, senior labelling leader to take end‑to‑end ownership of global product labelling across a defined portfolio.
This is a ha...
Monitor and provide guidance on European Union medical device regulations as the subject matter expert, ensuring device certification process compliance, and coordinating with internal teams to address future developments.Education and Experience RequirementsBachelors degree in Pharmaceutical Sciences or related.Special Skills RequirementsTwo (2) years of experience evaluating European Union Regula...
Locums, Inc. is seeking Primary Care Physicians for full-time Adult Primary care services in the Crownpoint Healthcare Facility in Crownpoint, NM. Assignment will be for 3 months with extensions possible. Any valid state or Federal license acceptable. About the Opportunity:- Period of Performance is approx. 7/1/20 to 9/30/20 w/ possible extension to 9/30/21- 10-hour shifts, 4 days a week. No weeken...
Job DescriptionDirector, Regulatory Affairs / Regulatory Services
Location: Remote – Applicants must be based in the Eastern or Central U.S. time zones.
Level: Director preferred; experienced Senior Managers will also be considered
Focus: US Regulatory Affairs / FDA
Reports to: Vice President, Regulatory Services
About the Role
We are seeking an experienced, hands-on Director of Regulatory Affai...
Job DescriptionPart of the Interparfums group founded in 1982, Interparfums USA develops, manufactures and distributes prestige fragrances as the exclusive worldwide licensee for Abercrombie & Fitch, Anna Sui, DKNY, Donna Karan, Graff, GUESS, Hollister, MCM, Oscar de la Renta, Roberto Cavalli, Salvatore Ferragamo and Ungaro. Through its global distribution network, the Company’s products are sold...
Sr. Regulatory Affairs SpecialistPosition SummaryThe Sr. Regulatory Affairs Specialist will be Responsible for regulatory affairs activities to assist in regulatory submission, annual reports, registrations and listings. Ensuring that the company adheres to all relevant laws, regulations, and standards. The position requires good knowledge of industry regulations and effective communication skills ...
Job DescriptionSummary
Land O’Frost is seeking a Manager, Corporate Regulatory Affairs to lead regulatory compliance and risk management efforts across our organization. This role will serve as a key partner to cross-functional teams, ensuring compliance with USDA regulations while supporting innovation, product launches, and operational excellence. This is a high-impact role responsible for guid...
Job DescriptionAbout Us:
Woof is the award-winning, innovative pet care brand on a mission to help dogs live happier, healthier lives through joyful play. Founded on the belief that the best products don't make you choose between what dogs need and what's good for them, we combine functional wellness, thoughtful design, and purpose-led play to strengthen dogs’ bodies, minds, and the bonds they sh...
Job DescriptionVP - Regulatory Policy
Join a team responsible for regulatory advocacy and advising senior management on how regulatory developments may affect the firm's capital position.
Evaluate the impact of existing and potential regulation on specific business activities, and advises desk heads on the regulatory capital implications of transaction structuring.
Additional functions include ...
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