Regulatory Affairs Advertising & Promotion, Manager**. At least 5 years of previous industry experience; 2 in Regulatory Affairs or in a role closely associated with the interpretation of medical and ...

Regulatory Affairs Advertising & Promotion, Manager**. At least 5 years of previous industry experience; 2 in Regulatory Affairs or in a role closely associated with the interpretation of medical and ...

Regulatory Affairs Manager II 12 Month Contract | REMOTE Join a leading biopharma company supporting critical regulatory systems initiatives. CTD submission managemen Regulatory, Regulatory Affairs, S...

With a special focus on student funding, this manager role oversees day-to-day functions of the Regulatory Affairs (RA) Funding team. The Regulatory Affairs Manager supports the department’s efforts t...

Regulatory Affairs Manager II 12 Month Contract | REMOTE Join a leading biopharma company supporting critical regulatory systems initiatives. CTD submission managemen Regulatory, Regulatory Affairs, S...

Requirements: Regulatory Operations & Regulatory Systems & submission process experience. Skills: GCP (Good Clinical Practice), Regulatory Affairs Operations. Key Focus Areas: Regulatory Systems Exp...

Skills: GCP (Good Clinical Practice), Regulatory Affairs Operations. Key Focus Areas: Regulatory Systems Expertise | eCTD Submission | Management Global Collaboration with IT & Regulatory Stakeholders...

Our client, a full range supplier of automotive coatings marketis seeking a Regulatory Affairs Managerto join their team. As a Regulatory Affairs Manager, you will be part of the management teamsuppor...

Our client, a full range supplier of automotive coatings marketis seeking a Regulatory Affairs Managerto join their team. As a Regulatory Affairs Manager, you will be part of the management teamsuppor...

Regulatory Affairs, Product Stewardship or EHS department at an industrial or manufacturing facility. Maintain and update regulatory systems for authoring SDSs, labels and regulatory content with chan...

Regulatory Affairs, Product Stewardship or EHS department at an industrial or manufacturing facility. Maintain and update regulatory systems for authoring SDSs, labels and regulatory content with chan...

Regulatory Affairs, Product Stewardship or EHS department at an industrial or manufacturing facility. Maintain and update regulatory systems for authoring SDS’s, labels and regulatory content with cha...

Compiles regulatory documents for FDA submission (eCTD experience preferred), which includes tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory...

Compiles regulatory documents for FDA submission (eCTD experience preferred), which includes tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory...

Compiles regulatory documents for FDA submission (eCTD experience preferred), which includes tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory...

Compiles regulatory documents for FDA submission (eCTD experience preferred), which includes tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory...

Compiles regulatory documents for FDA submission (eCTD experience preferred), which includes tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory...

Regulatory Affairs, Product Stewardship or EHS department at an industrial or manufacturing facility. Maintain and update regulatory systems for authoring SDS’s, labels and regulatory content with cha...

Compiles regulatory documents for FDA submission (eCTD experience preferred), which includes tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory...

Compiles regulatory documents for FDA submission (eCTD experience preferred), which includes tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory...

Compiles regulatory documents for FDA submission (eCTD experience preferred), which includes tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory...

Maintain and update regulatory systems for authoring SDS’s, labels and regulatory content with changing regulations. Regulatory Affairs, Product Stewardship or EHS department at an industrial or manuf...

Regulatory Affairs, Product Stewardship or EHS department at an industrial or manufacturing facility. Maintain and update regulatory systems for authoring SDS’s, labels and regulatory content with cha...

Regulatory Affairs Advertising & Promotion, Manager**. At least 5 years of previous industry experience; 2 in Regulatory Affairs or in a role closely associated with the interpretation of medical and ...

Regulatory Affairs Advertising & Promotion, Manager**. At least 5 years of previous industry experience; 2 in Regulatory Affairs or in a role closely associated with the interpretation of medical and ...

Provide expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and agency guidelines to assure compliance. With support from the Richardson quality team, ensure t...

Provide expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and agency guidelines to assure compliance. With support from the Richardson quality team, ensure t...

Our Senior Manager/Associate Director of Regulatory Affairs will work closely with our scientists, engineers, clinicians, quality professionals, and legal team to support our efforts to advance person...

Our Senior Manager/Associate Director of Regulatory Affairs will work closely with our scientists, engineers, clinicians, quality professionals, and legal team to support our efforts to advance person...

Serve as the principal regulatory affairs liaison to FDA and other health authorities for assigned Investigational New Drug (IND) and New Drug Applications (NDA) projects. Serve as the senior and prin...

Leverage your scientific and regulatory expertise to enable business growth (innovation, acquisitions) by collaborating on solutions to address regulatory and policy risks to grow and expand our curre...

Leverage your scientific and regulatory expertise to enable business growth (innovation, acquisitions) by collaborating on solutions to address regulatory and policy risks to grow and expand our curre...

Manager - Global Regulatory Affairs, you will be responsible for developing strategic global regulatory plans and preparing 510(k) submissions in support of new and existing marketing authorizations f...

Manager - Global Regulatory Affairs, you will be responsible for developing strategic global regulatory plans and preparing 510(k) submissions in support of new and existing marketing authorizations f...

The Manager, Regulatory Affairs - Licensing will be an active member of the Regulatory Affairs group within the Legal Department and will be responsible for assisting with regulatory compliance matter...

The Manager position in Regulatory Affairs contributes to the regulatory strategy for new and modified Sysmex medical device products. The Manager Regulatory Affairs is responsible for the preparation...

The Manager position in Regulatory Affairs contributes to the regulatory strategy for new and modified Sysmex medical device products. The Manager Regulatory Affairs is responsible for the preparation...

Regulatory Affairs Senior Manager is responsible for leading the regulatory strategy and managing the regulatory compliance in Personal Care and Cosmetics. Act as a regulatory representative with inte...

Regulatory Affairs Senior Manager is responsible for leading the regulatory strategy and managing the regulatory compliance in Personal Care and Cosmetics. Act as a regulatory representative with inte...

Perform change control assessment consistent with global regulatory guidance. Ensure global regulatory strategy and deliverables are aligned with project teams and business objectives. Communicate wit...