Regulatory Affairs Specialist

Job Description Job Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers. Join our team and contribute to our mission of...

Job DescriptionJob Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers. Join our team and contribute to our mission of...

Simply Good Foods is seeking a Regulatory Affairs Specialist to support continued growth. This is a critical role for the organization, supporting the Quest and Atkins brands in complying with regulations and laws at the ingredient and trade levels. Keys to success in this role: Strong background in Regulatory Labeling Regulations (US and Canada is a...

Sr. Regulatory Affairs Specialist Location: Los Angeles, Ca Company Size : 200/ Team Size : 15 Duties & Responsibilities: Manage all regulatory activities necessary to maintain and to grow the business. Develop and implement regulatory strategies for new and existing products regulated under the OTC Monographs and Cosmetic regulatory designations. Serve as a...

Sr. Regulatory Affairs SpecialistLocation: Los Angeles, CaCompany Size: 200/ Team Size: 15Duties & Responsibilities:Manage all regulatory activities necessary to maintain and to grow the business. Develop and implement regulatory strategies for new and existing products regulated under the OTC Monographs and Cosmetic regulatory designations.Serve as a...

Sr. Regulatory Affairs SpecialistLocation: Los Angeles, CaCompany Size: 200/ Team Size: 15Duties & Responsibilities:Manage all regulatory activities necessary to maintain and to grow the business. Develop and implement regulatory strategies for new and existing products regulated under the OTC Monographs and Cosmetic regulatory designations.Serve as a...

Sr. Regulatory Affairs Specialist Location: Los Angeles, Ca Company Size: 200/ Team Size: 15 Duties & Responsibilities: Manage all regulatory activities necessary to maintain and to grow the business. Develop and implement regulatory strategies for new and existing products regulated under the OTC Monographs and Cosmetic regulatory designations. Serve as a...

Sr. Regulatory Affairs SpecialistLocation: Los Angeles, CaCompany Size: 200/ Team Size: 15Duties & Responsibilities:Manage all regulatory activities necessary to maintain and to grow the business. Develop and implement regulatory strategies for new and existing products regulated under the OTC Monographs and Cosmetic regulatory designations.Serve as a...

Client: IRIDEX Position: Regulatory Affairs Associate Location: Mountain View, CA Contract Length: 5 months Pay Range: $35 - $45/hr IRIDEX Corporation is a medical device manufacturer and operates in a global regulated environment (e.g. FDA). Regulations include (but are not limited to) FDA 21 CFR 820, EN ISO 13485, Health Canada SOR/ 98-282, and the...

19901 Nordhoff St, Northridge, CA 91324, USA Job Description Posted Thursday, April 4, 2024 at 4:00 AM K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world....

Meets clinical-stage biopharmaceutical client based in the Bay Area is seeking a highly motivated individual to join their growing regulatory affairs group. The Associate Director / Director, Regulatory Affairs will work closely with the Regulatory Affairs team and other departments to develop and implement regulatory strategies for the company's rare...

NO AGENCIES! - pl do not submit. W2 candidates only Scope To support business in maintaining regulatory compliance of existing manufactured products for customers on a global basis. Managing regulatory compliance activities and existing customer products and registrations as required and providing strategic planning for regulatory changes. Acting as the...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill Coordinator Location: 91342, Los Angeles, California, United States Duration: 06 Month Job Description: This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. ...

JSHealth Vitamins is seeking a Regulatory Affairs Manager to join our dynamic team in Westwood, Los Angeles. We are a leading science-focused vitamin and wellness brand that provides targeted formulas to help customers meet their personal health goals. Our founder, Jessica Sepel, is a best-selling health author who founded JSHealth Vitamins to provide her...

JSHealth Vitamins is seeking a Regulatory Affairs Manager to join our dynamic team in Westwood, Los Angeles. We are a leading science-focused vitamin and wellness brand that provides targeted formulas to help customers meet their personal health goals. Our founder, Jessica Sepel, is a best-selling health author who founded JSHealth Vitamins to provide her...

19901 Nordhoff St, Northridge, CA 91324, USA Job Description Posted Tuesday, March 19, 2024 at 4:00 AM K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world....

NO AGENCIES! - pl do not submit.W2 candidates only***NOTE If this opportunity interests you, please share a WORD resume that details your exp related to the job responsibilities and requirements.ScopeTo support business in maintaining regulatory compliance of existing manufactured products for customers on a global basis.Managing regulatory compliance...