The Senior Regulatory Affairs Specialist sits within the Animal Health organisation and reports to the Regulatory Affairs Manager. The primary responsibility of the Senior Regulatory Affairs Specialis...

The Senior Regulatory Affairs Specialist sits within the Animal Health organisation and reports to the Regulatory Affairs Manager. The primary responsibility of the Senior Regulatory Affairs Specialis...

The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with globa...

The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with globa...

Technology Regulatory Affairs Specialist.

Technology Regulatory Affairs Specialist.

Sr Specialist, Regulatory Affairs CMC. Maintain regulatory information in accordance with processes and procedures to support regulatory compliance. Work independently and effectively with other funct...

Sr Specialist, Regulatory Affairs CMC. Maintain regulatory information in accordance with processes and procedures to support regulatory compliance. Work independently and effectively with other funct...

Sr Specialist, Regulatory Affairs CMC.

Sr Specialist, Regulatory Affairs CMC.

Quality and Regulatory Affairs Specialist. Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New Y...

Quality and Regulatory Affairs Specialist. Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New Y...

The Senior Regulatory Affairs Specialist is responsible for managing appropriate regulatory and technical information to ensure regulatory compliance and support product registrations globally. Assist...

The Senior Regulatory Affairs Specialist is responsible for managing appropriate regulatory and technical information to ensure regulatory compliance and support product registrations globally. Advise...

The Regulatory Affairs Specialist (F&B) will be responsible to independently provide Symrise Inc. The Regulatory Affairs Specialist may provide support to the retrieval of revenue paid for the use of ...

Monitor regulatory trends and FDA guidance updates, proactively integrating these insights into product evolution. Demonstrated expertise in FDA regulatory requirements and promotional content complia...

The Regulatory Affairs Specialist (F&B) will be responsible to independently provide Symrise Inc. The Regulatory Affairs Specialist may provide support to the retrieval of revenue paid for the use of ...

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...

Experience working on regulatory or governmental matters, directly or in a support role, with state energy regulators or legislators; a diversity of operational or staff position experience working fo...

Experience working on regulatory or governmental matters, directly or in a support role, with state energy regulators or legislators; a diversity of operational or staff position experience working fo...

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...

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...

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...

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

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Compile, prepare, and review regulatory submission to US and EU. Anticipate regulatory obstacles and emerging is...

Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within th...

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.

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. Ensuring outgoing Reg...

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...

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...