Job Title: Associate Principal Scientist, Regulatory Affairs. R&D sciences discipline (engineering, chemistry, biological sciences, pharmacy, veterinary, regulatory). Required: minimum of 2 years auth...

Job Title: Associate Principal Scientist, Regulatory Affairs. R&D sciences discipline (engineering, chemistry, biological sciences, pharmacy, veterinary, regulatory). Required: minimum of 2 years auth...

Job Title: Associate Principal Scientist, Regulatory Affairs. R&D sciences discipline (engineering, chemistry, biological sciences, pharmacy, veterinary, regulatory). Required: minimum of 2 years auth...

Job Title: Associate Principal Scientist, Regulatory Affairs. R&D sciences discipline (engineering, chemistry, biological sciences, pharmacy, veterinary, regulatory). Required: minimum of 2 years auth...

Position requires a Bachelor's degree in a science or chemistry-related field, coursework or certification in Cosmetic or Drug Regulatory Affairs. Canada Chemical regulatory oversight and review.

Provide regulatory support for new product registrations, Certificates of Free Sale, labeling compliance, SDS authoring, PIF preparation per various international specific country registration require...

Position requires a Bachelor's degree in a science or chemistry-related field, coursework or certification in Cosmetic or Drug Regulatory Affairs. Canada Chemical regulatory oversight and review.

The Labeling Specialist supports the development of labeling activities for all regulatory submissions. Effective collaboration with Regulatory Affairs, CMR, Supply Chain, and HQ colleagues regarding ...

The Labeling Specialist supports the development of labeling activities for all regulatory submissions. Effective collaboration with Regulatory Affairs, CMR, Supply Chain, and HQ colleagues regarding ...

The requirement is for 3 Regulatory Affairs Specialist. Facilitate worldwide product registration activities by compiling appropriate dossiers, submissions and responses to regulatory bodies. Maintain...

The requirement is for 3 Regulatory Affairs Specialist. Facilitate worldwide product registration activities by compiling appropriate dossiers, submissions and responses to regulatory bodies. Maintain...

The Regulatory Affairs Specialist will support the Director of Regulatory Affairs and collaborate with various departments to complete international product registrations (Canada, Southeast Asia, Midd...

The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regula...

The Regulatory Affairs Specialist coordinates, facilitates, and reports on post-market regulatory programs. Implements regulatory activities such as obtaining global regulatory clearances and/or appro...

The Regulatory Affairs Specialist coordinates, facilitates, and reports on post-market regulatory programs. Implements regulatory activities such as obtaining global regulatory clearances and/or appro...

Provide consultation and advice to regulatory specialists regarding change control and product development. Contribute to continuous improvement initiatives within the regulatory affairs function. Abi...

Provide consultation and advice to regulatory specialists regarding change control and product development. Contribute to continuous improvement initiatives within the regulatory affairs function. Abi...

The Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...

The Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Monitor and submit applicable reports and ensure appropriate responses are submitted to regulatory authorities. ...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Provide regulatory input for responsible countries/region for product lifecycle planning. Provide strategic inpu...

Regulatory Affairs or equivalent industry experience is required. Knowledge in relevant Regulatory Affairs areas. Maintains advanced and current knowledge of relevant regulations, policies, and guidel...

This position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulat...

Eligibilities & qualifications.

The Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. Assisting in gatherin...

The Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. OTC regulatory experi...

Prepare new/revised label packaging for regulatory submissions to the USDA and maintain regulatory documents to ensure site compliance. Support regulatory filing submissions with the USDA for both dom...

Prepare new/revised label packaging for regulatory submissions to the USDA and maintain regulatory documents to ensure site compliance. Support regulatory filing submissions with the USDA for both dom...

Regulatory Affairs Specialist Project Lead I (Scientific). At least - years of relevant pharmaceutical/biotechnology experience in R&D, including at least years of relevant Regulatory Affairs experien...

Regulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...

Regulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...

Provide guidance to the company and subsidiaries to perform actions in order to maintain regulatory compliance for various facilities. Develop appropriate awareness and training programs for TSMs cons...

Provide guidance to the company and subsidiaries to perform actions in order to maintain regulatory compliance for various facilities. Develop appropriate awareness and training programs for TSMs cons...

This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Stra...

Regulatory expert support IVDR teams, implements regulatory strategies for IVDR activities; provides regulatory leadership; collaborates with the regulatory staff from other business units, companies,...

Regulatory expert support IVDR teams, implements regulatory strategies for IVDR activities; provides regulatory leadership; collaborates with the regulatory staff from other business units, companies,...

Analyzes and communicate the adequacy of proposed regulatory pathways and strategy for initial product designs and recommend changes or refinements based on initial regulatory outcomes. Write and revi...

Analyzes and communicate the adequacy of proposed regulatory pathways and strategy for initial product designs and recommend changes or refinements based on initial regulatory outcomes. Write and revi...