Regulatory Affairs Consultant

Position Summary The primary responsibility of the Regulatory Affairs Specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies. The RAS is also responsible for ensuring products and procedures comply with regulatory agency specifications. Supports necessary regulatory activities required for our client's product...

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...

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 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...

Vice President Regulatory Affairs (Medical Device) - ONSITE in Bay Area Our esteemed client, a inovative and growing medical device company specializing in the manufacturing of implantable medical devices. They are looking for a Vice President Regulatory Affairs to spearhead regulatory strategies that will shape the future of healthcare and continue building...

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 Description Job DescriptionPureTek 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...

Manager, Regulatory Affairs **Job Category**:Accounting/Finance**Department**:Compliance**Location**:Los Angeles, CA, US, 90017**Position Type**:Full Time**Requisition ID**:11212**Salary Range**: $102,183.00 (Min.) - $132,838.00 (Mid.) - $163,492.00 (Max.)- Established in 1997, L.A. Care Health Plan is an independent public agency created by the state of...

Senior Regulatory Affairs Specialist (Medical Devices) - Hybrid (Bay Area) Our client is a growing Imaging Medical Device company that is making a meaningful impact on patient lives. They are looking for a Senior Regulatory Affairs Specialist with a track record of bringing imaging devices to market. Responsibilities: Prepare and submit regulatory...

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. ...

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...

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 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...

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....

Job DescriptionJob DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Director/Sr. Director, CMC Regulatory Affairs to work for a leading Greater Los Angeles area biotechnology company.The Director/Sr. Director, CMC Regulatory Affairs is...

Job DescriptionJob DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Director/Sr. Director, CMC Regulatory Affairs to work for a leading Greater Los Angeles area biotechnology company.The Director/Sr. Director, CMC Regulatory Affairs is...