Regulatory Affairs Specialist Responsible for ensuring that the organizations activities are conducted ethically and in compliance with relevant regulations, laws, and standards. Develops and implements regulatory strategies, procedures, and controls for new products and/or business activities
Regulatory CMC Manager Cell and Gene Therapy Updated: Today Location: Tlalnepantla, MEX, Mexico Job ID: -OTHLOC-7302-2DR Description Regulatory CMC Manager Cell and Gene Therapy Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer
Updated: TodayLocation: Tlalnepantla, MEX, MexicoJob ID: -OTHLOC- DRJob ResponsibilitiesGeneral Position SummaryThe Device CMC manager will support strategies for marketed and development products. This role contributes to the preparation and submission of regulatory CMC documentation for device part of
Description Regulatory Consultant CMC - Biologics Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Syneos Health, Inc. in Mexico is seeking a Device CMC Manager to support regulatory submissions for device components of combination products. You will guide cross‑functional teams to ensure global regulatory requirements are incorporated into development and commercial
About Freyr Freyr Solutions is a leading global Regulatory Solutions and Services company supporting Life Sciences organizations across pharmaceuticals, biologics, medical devices, and consumer healthcare industries. Freyr partners with global clients to deliver specialized regulatory, compliance,
Regulatory Affairs Officer, IQVIA BiotechServe as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing.Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level.Engage directly