Regulatory affairs specialist Jobs in USA
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Regulatory affairs specialist • usa
Last updated: 1 hour ago
PM-International is one of Europe’s leading direct selling companies, specializing in health, fitness, and beauty products for over 25 years.
Headquartered in Sarasota, Florida, for the Americ...Show moreLast updated: 7 days ago
We are seeking a Regulatory Affairs Specialist with a strong background in oral solid dose pharmaceuticals and hands-on experience with CMC (Chemistry, Manufacturing & Controls) to support regu...Show moreLast updated: 2 days ago
At Kaléo our way is not to seek to be like others but rather to passionately pursue meaningful and innovative solutions for patients.
We believeall people should have access to the innovative health...Show moreLast updated: 16 hours ago
Qualifications EDUCATION : Bachelors degree in environmental science chemistry toxicology environmental engineering or other applicable related degree.
Advanced degree in environmental science chemis...Show moreLast updated: 2 days ago
Stefanini is looking for a Regulatory Affairs Specialist in Glenview IL 60025 (Hybrid).For quick apply please reach out to Madelaine MADIE Yu.
Waukegan Rd Glenview IL 60025 (Hybrid - in office Tues-...Show moreLast updated: 6 days ago
Scope Of Responsibilities : He / She will be responsible for representing regulatory function to approve promotional material He / She will be at ease working in a matrix environment and be able to na...Show moreLast updated: 29 days ago
Job Summary Under general supervision, the Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals....Show moreLast updated: 11 hours ago
Working with an exciting biotech company that has grown by over 75% in the last two years and is looking for a regulatory affair specialist to enhance their team.
This company is focusing on pushing...Show moreLast updated: 9 hours ago
Regulatory Affairs Specialist / h2pResponsibilities : The Regulatory Affairs Specialist will be responsible for supporting regulatory activities for existing US FDA class III medical devices.This role...Show moreLast updated: 4 days ago
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 commitment...Show moreLast updated: 14 days ago
CorDx, a multi-national biotech organization, focused on pushing the limits of innovation and supply in global health.With over 2000 employees across the world serving millions of users in over 100...Show moreLast updated: 14 days ago
Willert Home Products is a leading manufacturing company specializing in the production of high-quality yet cost-effective consumer products.
With a commitment to innovation, efficiency, and excelle...Show moreLast updated: 14 days ago
A company is looking for a Regulatory Affairs Specialist, IV.Key Responsibilities Develop and implement global regulatory strategies and prepare submissions for regulatory approvals Provide regu...Show moreLast updated: 1 day ago
We anticipate the application window for this opening will close on - 16 Feb 2026.At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare acces...Show moreLast updated: 1 day ago
Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product...Show moreLast updated: 1 hour ago
Job Summary : The Regulatory Affairs Specialist will provide support to the Director of Regulatory Affairs in relation to the Company's regulatory compliance efforts.
Assist in managing regulatory af...Show moreLast updated: 30+ days ago
Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or equivalent combination of education and experience, including preparation and submission of pesticide...Show moreLast updated: 1 day ago
Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 14 days ago
Evolution Research Group (ERG) is dedicated to delivering high-quality Phase IIV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely...Show moreLast updated: 12 hours ago
- Promoted
Regulatory Affairs Specialist
PM-International USASarasota, FL, USFull-time
- Promoted
Regulatory Affairs Specialist
Planet PharmaBristol, TN, USFull-time
- New!
Specialist, Regulatory Affairs
KaléoRichmond, Virginia, USAFull-time
Regulatory Affairs Specialist
Real Soft IncTrumbull, Connecticut, USAFull-time
Regulatory Affairs Specialist
Stefanini GroupGlenview, Illinois, USAFull-time
- Promoted
Regulatory Affairs Specialist
AequorSan Diego, CA, USFull-time
- Promoted
- New!
Regulatory Affairs Specialist
Medline Industries - Transportation & OperationsNorthfield, Illinois, United StatesFull-time
- New!
REGULATORY AFFAIRS SPECIALIST
Barrington JamesNew York, NY, United StatesFull-time
- Promoted
Regulatory Affairs Specialist
Katalyst Healthcares Life SciencesSan Francisco, CA, USFull-time
Regulatory Affairs Specialist
HP HoodWilmington, MA, USFull-time
Regulatory Affairs Specialist
CorDxAlpharetta, GA, USFull-time
Regulatory Affairs Specialist
Willert Home ProductsSaint Louis, MO, USFull-time
- Promoted
Regulatory Affairs Specialist
VirtualVocationsRedding, California, United StatesFull-time
Regulatory Affairs Specialist
MedtronicMinneapolis, Minnesota, USAFull-time
- New!
Regulatory Affairs Specialist
PhilipsBoston, MA, United StatesFull-time
- Promoted
Regulatory Affairs Specialist
iHerbIrvine, CA, USFull-time
Regulatory Affairs Specialist
GlobalchannelmanagementTrumbull, Connecticut, United StatesFull-time
- Promoted
Regulatory Affairs Specialist
AbbottSanta Clara, CA, USFull-time
- Promoted
- New!
Regulatory Affairs Specialist
Evolution Research GroupMiami, FL, USFull-time
The average salary range is between $ 73,827 and $ 125,960 year , with the average salary hovering around $ 93,223 year .
Regulatory Affairs Specialist
PM-International USASarasota, FL, US7 days ago
Job type
- Full-time
Job descriptionBachelor’s degree in Life Sciences, Pharmacy, Chemistry, or related field. 3+ years of regulatory affairs experience in dietary supplements, cosmetics, food, or pharmaceuticals. Strong knowledge of U.S. FDA regulations and experience with Latin American regulatory frameworks. Bilingual English–Spanish ; Portuguese is a plus. Strong organizational and communication skills, with the ability to manage multiple projects across countries. Be part of an international, fast-growing company with a mission to bring high-quality products to consumers worldwide. Work in a diverse, multicultural environment supporting multiple regions. Opportunity to grow your expertise in global regulatory affairs. Competitive compensation and benefits package. Salary Range : $60,000 - $75,000
Job Description
Company Description
PM-International is one of Europe’s leading direct selling companies, specializing in health, fitness, and beauty products for over 25 years. Headquartered in Sarasota, Florida, for the Americas region, the company combines innovative thinking, scientific excellence, and high manufacturing standards to deliver premium products that enhance well-being. With a global reach and a diverse, multicultural workforce, PM-International fosters a collaborative and inclusive environment. The organization prioritizes supporting personal and professional growth, offering employees opportunities to make meaningful contributions and thrive in their careers.
Role Description
The Regulatory Affairs Specialist is an on-site, full-time position located in Sarasota, FL. In this role, you will handle regulatory documentation, ensure compliance with regulatory requirements, oversee regulatory submissions, and support the company in all matters related to regulatory affairs across the United States, Central America, and South America. You will work closely with internal teams and regulatory agencies to maintain adherence to industry standards and guidelines, contributing to the development and distribution of high-quality products.
What You’ll Do
- Prepare and submit product registration dossiers and notifications across the Americas.
- Ensure compliance of labels, claims, and packaging with local regulations (FDA, INVIMA, ANVISA, COFEPRIS, etc.).
- Maintain regulatory documentation and approvals for ongoing compliance.
- Serve as the liaison with local regulatory authorities, consultants, and distributors.
- Monitor regulatory updates in the USA, Central America, and South America, and advise internal teams.
- Support new product development with regulatory guidance and review of marketing materials.
What We’re Looking For
Why Join Us?