Description: Responsible for the strategy and execution of the site-specific aspects of the preparation of CMC post-market supplements and facility registrations Interfaces with site functions to coordinate preparation of regulatory filings, identification of issues and factors that may implicate a …read more
Regulatory Affairs Specialist III # JN -072021-67095
Description: Role Overview The Regulatory Affairs Sr Specialist develops and executes the regulatory submissions plans, ensuring deadlines are met and documents are properly formatted, complete, and in compliance with pharmaceutical/biologics regulatory requirements The Regulatory Affairs Manager will supervise direct reports …read more
Regulatory Specialist # JN -072021-66588
Job Description: Provide guidance and training to area personnel regarding regulatory compliance. Prepare and file FCC/FAA applications and supporting documentation concerning tower erection, modifications and antenna installations Review permits and documents to track compliance with regulations and company policy Review …read more
Manager, Regulatory Information Management # JN -062021-65819
Title: Manager, Regulatory Information Management Location: Cambridge, MA Job Type: Long Term Contract Job Description: Requires understanding the regulatory customer perspective, ability to translate to the data and the data model in the RIM Ecosystem. The role is expected to take direction from …read more
Regulatory Affairs Specialist IV #JN -052021-64303
Description: The Regulatory Affairs Specialist will develop and implement regulatory strategies, focused on Orthopedic products and on achieving compliance with the upcoming European Medical Device Regulation. The Regulatory Affairs Specialist will be responsible for providing regulatory input and strategic direction …read more
