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. The Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceut...

Job Title: Associate Principal Scientist, Regulatory Affairs. The Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceut...

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.

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.

Effective collaboration with Regulatory Affairs, CMR, Supply Chain, and HQ colleagues regarding labeling compliance to accomplish company goals. This individual works cross-functionally with internal ...

Effective collaboration with Regulatory Affairs, CMR, Supply Chain, and HQ colleagues regarding labeling compliance to accomplish company goals. This individual works cross-functionally with internal ...

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...

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

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...

Support daily Regulatory Affairs function eg; compliance to CFR ,, ISO requirements, Company policies, operating procedures, processes, promotional task assignments into windchill and assigned trainin...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Compile, prepare, and review regulatory submission to US and EU. Provide strategic input and technical guidance ...

Regulatory Affairs or equivalent industry experience is required. Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of client's prod...

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...

Hiring - Senior Regulatory Affairs Specialist. Assess applicable change requests for regulatory impact and follow-up on related regulatory action items. Support marketing, R&D and Lonza BU in ad hoc p...

Eligibilities & qualifications.

Must make a proactive contribution to the overall Regulatory affairs department growth. Determine appropriate regulatory requirements and strategies for new product development projects including both...

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...

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...

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 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...

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,...

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. Reviews and as...

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. Reviews and as...