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 DescriptionPBS, one of the country's leading public media organizations, has engaged Garrison to assist in its search for a Corporate Counsel with 4+ years of corporate experience. This is an excellent opportunity to join a highly regarded, close-knit legal team within one of the most collegial and mission-driven organizations in the DMV.
Reporting to the Deputy General Counsel, the Corporate ...
Partner Affairs Open
Partner Affairs Open
Job DescriptionWorking with an exceptional law firm, we are proud to be leading the search for a Partner Affairs professional based in their New York office.
As part of a wider team, this is a key role that will focus on supporting and enabling partner insights, integration, and governance across the firm.
Key Responsibilities
Support governance and management activities across the partner life...
Job DescriptionJob Title: Corporate Marketing Manager
Location: Onsite - Bergen County, NJ
Contract to Hire: 6 months contract to permanent
Pay Range: $35-45/hour (W2)
About TSR
TSR is a trusted staffing and workforce solutions partner with more than 50 years of experience delivery highly qualified talent to support clients' most critical business and technology initiatives. Through a disciplined ...
Job DescriptionJob Description for:
Corporate Marketing Manager / LGEUS NA Innovation Center Marketing Lead
LG Electronics seeks a dynamic, community-minded person with corporate and group engagement experience to support programming for the LG Inspiration Lab™, visitor engagement for LG Electronics N. America Innovation Campus (NAIC) and other corporate marketing and partnership initiatives.
T...
Job DescriptionTyra Biosciences, Inc. is seeking a highly motivated and experienced Vice President of Medical Affairs to make impactful contributions to multiple oncology programs targeting disease areas with high unmet medical need. The successful candidate will be highly organized, self-motivated, and thrive in a dynamic, cross functional start-up environment.
This position is responsible for le...
Job DescriptionSummary:
The Scientific Affairs Manager is responsible for translating scientific evidence into accurate, compelling, and commercially-relevant scientific communications in support of Everwell Health ingredients. Reporting to the Senior Scientific Affairs manager, this role supports day-to-day scientific affairs activities and serves a key scientific partner to Marketing and Sales, ...
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, ...
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 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 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 DescriptionJob Title: Foreign Affairs Specialist
Job Code: CON113
Location: Washington, DC
Reports to: Program Manager
FLSA Status: Exempt
Supervisory: No supervisory/management authority
Prepared Date: 10/14/2026
A government contract requires that this position be restricted to U.S. citizens or legal permanent residents. You must provide documentation that you are a U.S. citizen or le...
Job DescriptionGovernment Affairs Associate
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Position Summary
Powering Prosperity is seeking a proactive and resourceful professional to help advance state-based energy advocacy and support the development of innovative, market-oriented policy solutions.
The Government Affairs Associate is intentionally designed as a leadership development role. The sso...
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...
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