Regulatory Submissions Document Reviewer

March 7

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Bureau Veritas Group

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Bureau Veritas Group is a global leader in testing, inspection, and certification services. With a mission to shape a world of trust, the company serves 400,000 clients across 140 countries, ensuring that various industries meet quality, health, safety, and environmental standards. Bureau Veritas is committed to providing innovative services that enhance safety, improve efficiency, and support sustainable development.

SERVICES • TESTING • INSPECTION • CERTIFICATION • CLASSIFICATION

10,000+ employees

Founded 1828

📋 Compliance

🏢 Enterprise

📋 Description

• Responsible for reviewing nonclinical regulatory documents for various client departments. • Complete Quality Review to ensure consistency and accuracy within and across nonclinical regulatory submission documents. • Provide technical leadership, which could include project design and technical troubleshooting and support. • Communicate and work with PhD level scientists and review their reports for data conclusions and accuracy. • Perform annual review literature searches. • Assist in writing nonclinical sections in the regulatory documents. • Follow the guidelines set forth with clients and in the company Quality, Health, Safety and Environmental policies and procedures. • Comply with clients and company management systems in accordance with appropriate regulatory agencies. • Follow the guidelines set forth by clients in the company Quality Manual and Safety/Chemical Hygiene Plan. • Other duties as defined by Manager, department needs and workload.

🎯 Requirements

• PhD in Science - Biology, Microbiology or Neuroscience preferred. • Minimum of six (6) months related experience such as: • Providing technical consultation and data review • Completing document review, formatting standards, Quality Control, and editing • Developing training manuals, SOP’s and hands on teaching • An equivalent combination of education and experience may be accepted in lieu of above.