- System One (Florham Park, NJ)
- Job Title: Manager, Regulatory Operations Documentation Specialist - Contractor Location: Florham Park, New Jersey - hybrid 50% Type: Contract Compensation: ... - $85 hourly Overview This role will lead the Regulatory Operations - Documentation Specialist ...formatting, remediation and quality control (QC) of documentation for submissions to Health Authorities. It also includes the archiving… more
- Medtronic (Irvine, CA)
- …partners with the international regulatory affairs group to support regulatory submissions . Sustaining regulatory responsibilities include reviewing ... compassionate world. **A Day in the Life** The Sr Regulatory Affairs Specialist will play a key...the international regulatory affairs group to support regulatory submissions . Sustaining regulatory responsibilities… more
- BD (Becton, Dickinson and Company) (Covington, GA)
- … Affairs Specialist I is responsible for implementation of regulatory strategies including domestic and international submissions and other support ... Affairs Specialist I are responsible for implementation of regulatory strategies including domestic and international submissions and other support… more
- UPMC (Pittsburgh, PA)
- …of cancer. UPMC Hillman Cancer Center is currently hiring a regular full-time ** Regulatory Specialist ** to help support the Oncology Clinical Research Services ... trial activation process while working Monday through Friday daylight hours. The Regulatory Specialist 's purpose is to develop regulatory forms/documents… more
- Philips (Plymouth, MN)
- …submissions , Pre- Submissions , EU MDR Technical Documentation, and global regulatory submissions , ensuring robust compliance and strategic alignment. Drive ... Join RespirTech's team in Plymouth, MN as a Principal Regulatory Affairs Specialist , where you will develop...Pre- Submissions , EU MDR Technical Documentation, and global regulatory submissions /registrations. + You have expertise in… more
- J&J Family of Companies (Santa Clara, CA)
- …In collaboration with cross-functional team members, compile, prepare, review and submit high-quality regulatory submissions to authorities on time in US and EU. ... Description:** Johnson & Johnson is hiring for a **Sr Regulatory Affairs Specialist ** **- Shockwave** to join...Support international regulatory team with submissions to other geographies… more
- J&J Family of Companies (Santa Clara, CA)
- …In collaboration with cross-functional team members, compile, prepare, review and submit high-quality regulatory submissions to authorities on time in US and EU. ... Description:** Johnson & Johnson is hiring for a **Sr.** ** Regulatory Affairs Specialist (Remote) - Shockwave Medical**...Support international regulatory team with submissions to other geographies… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …compliance. They participate on cross-functional teams, lead the development of global regulatory strategies, author regulatory submissions , interact with ... Become a **maker of possible** with us. The Sr. Regulatory Affairs Specialist independently supports projects to...labeling in consideration of US, EU, and other global regulatory requirements. + Authors FDA submissions , EU… more
- Medtronic (Lafayette, CO)
- …requirements + Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and ... compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible...standards + Create or revise departmental procedures to improve operations or to reflect changing regulatory requirements… more
- Abbott (Santa Clara, CA)
- …clinical documentation for submission filing. + Compile, prepare, review and submit regulatory submissions to authorities. + Monitor impact of changing ... catheters and software, vessel closure devices and peripheral stents. This **Senior Regulatory Affairs Specialist ** position is an onsite opportunity working out… more
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