We are an innovative AI company transforming the Medical, Legal, and Regulatory (MLR) review process for the pharmaceutical industry. Leveraging cutting-edge technology, we automate and enhance conten...

Leveraging cutting-edge technology, we automate and enhance content review, compliance management, and strategic alignment of promotional materials, streamlining workflows to drive faster, more accura...

We are seeking a highly motivated individual to join our team as a Regulatory Affairs (RA) Specialist responsible for supporting the regulatory compliance of medical devices in the EMEA and LATAM regi...

Technology Regulatory Affairs Specialist.

Technology Regulatory Affairs Specialist.

We are seeking a highly motivated individual to join our team as a Regulatory Affairs (RA) Specialist responsible for supporting the regulatory compliance of medical devices in the EMEA and LATAM regi...

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

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...

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...

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...

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...

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...

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...

Our Senior Regulatory Affairs Specialist position is primarily focused on maintaining continued market access of our existing product portfolio, in addition to opportunities to provide regulatory supp...

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 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 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...

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) ...

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...

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. Practical experience in leading cross-functional teams on regulatory and compliance related projects. Compile, p...

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.

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. Assisting in gatherin...

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 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...

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...

At least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development. T...

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...