The Senior Regulatory Affairs Specialist is responsible for the successful implementation of regulatory goals and objectives. Accountable for creating a culture of continuous regulatory readiness thro...

Job Summary
Under general supervision, the Regulatory Specialist is responsible for planning and executing regulatory activities necessary to bring new Over-the-Counter (OTC) Drugs and Cosmetics to...

CooperSurgical is at the forefront of d Regulatory Affairs, Specialist, Regulatory, Healthcare, Manufacturing, Surgical.

The Senior Regulatory Affairs Specialist will work in BD Specimen Management providing regulatory leadership to cross-functional project teams from early development to new product launches in variou...

The Senior Regulatory Affairs Specialist will work in BD Specimen Management providing regulatory leadership to cross-functional project teams from early development to new product launches in variou...

Technology Regulatory Affairs Specialist. We are seeking a dynamic and detail-oriented Technology Regulatory Affairs Specialist. Our client, a major bank in New York City, is looking for talented Tech...

CooperSurgical is at the forefront of d Regulatory Affairs, Specialist, Regulatory, Healthcare, Manufacturing, Surgical.

We are seeking a dynamic and detail-oriented Technology Regulatory Affairs Specialist. Technology Regulatory Affairs Specialist. Our client, a major bank in New York City, is looking for talented Tech...

Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...

Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...

Job Title: Global Regulatory Affairs - CMC Specialist. R&D sciences discipline (engineering, chemistry, biological sciences, pharmacy, veterinary, regulatory). Required: minimum of 2 years authoring C...

Job Title: Global Regulatory Affairs - CMC Specialist. R&D sciences discipline (engineering, chemistry, biological sciences, pharmacy, veterinary, regulatory). Required: minimum of 2 years authoring C...

Job Title: Global Regulatory Affairs - CMC Specialist. Experience authoring technical reports and regulatory submissions, experience reviewing scientific information, with sound judgement and attentio...

Job Title: Global Regulatory Affairs - CMC Specialist. S with >10 years relevant industry experience in related R&D sciences discipline (engineering, chemistry, biological sciences, pharmacy, veterina...

The requirement is for 3 Regulatory Affairs Specialist. The candidates will work with client & Our client's teams to deliver best in-class solutions for regulatory submissions. Facilitate worldwide pr...

Job Title: Global Regulatory Affairs - CMC Specialist.

Job Title: Global Regulatory Affairs - CMC Specialist.

Regulatory Affairs Project management experience. Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects a...

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

Performs quality control, research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring that Good Clinical Practices (GCP) ...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Anticipate regulatory obstacles and emerging issues throughout the product submission. Provide regulatory input ...

Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of client's products and processes. Knowledge in relevant Regulatory Affairs areas...

Eligibilities & qualifications.

Working knowledge of relevant federal and state regulatory programs (e.

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. Assisting in gatherin...

Regulatory Affairs Specialist Project Lead I (Scientific). This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be res...

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). This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be res...

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...

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...