Regulatory Submissions Manager jobs

Viewing 1 - 10 of 1,007 jobs

• Science Submission Manager (Scientific Writing)

  Medimmune - Maryland

  providers * Provides guidance to staff on regulatory submissions and development reports ~BSP Position: 3-4 years ... Masters degree in a scientific discipline is acceptable with 4-5 years of laboratory and/or regulatory writing work expe...

  8 days ago from BioSpace

• Quality Systems and Regulatory Affairs Manager

  Tp Orthodontics - Westville, IN

  lead Regulatory Affairs officer to manage compliance with regulatory requirements in a global market environment, ... with regulatory agencies including coordination of submissions for regulatory approvals to market (510K),...

  20 hours ago from CareerBuilder

• Research Regulatory Specialist

  Catholic Health Initiatives - Englewood, CO

  * Act as a liaison between the Clinical Project Manager, regulatory agencies, and the Investigators to seek protocol ... required regulatory files for all clinical trials to ensure regulatory compliance (CVs, licensure, research...

  24 days ago from MiracleWorkers.com

• Manager, Regulatory Affairs

  FPC of Mandeville - South Carolina

  edical device company is conducting a search for a Manager, Regulatory Affairs: Candidate will manage all company ... BS in Life Sciences, minumum 6 years regulatory experience within the medical device/pharmaceutical industry, with at le...

  30+ days ago from ResumeSpider

• Regulatory and Quality Affairs Specialist

  Young Innovations - Earth City, MO

  OverviewThe Regulatory and Quality Affairs Specialist is a key member on our integrated Quality and Regulatory Team and ... government bodies, and external certifications for CE marks-Regulatory research and review for new products/materials...

  8 days ago from CareerBuilder

• Manager, Regulatory Affairs

  Cameron Craig Group - Pittsburgh, PA

  Manager of Regulatory Affairs The ideal candidate will be responsible for managing a staff Regulatory Affairs Engineers ... oversee the preparation and submission of all regulatory submissions for device approvals and...

  30+ days ago from Cameron Craig Group

• Submission Writer / Senior Submission Writer

  Novartis Pharmaceuticals - East Hanover, NJ

  Act as liaison between clinical trial teams and document publishing and/or regulatory operations to ensure timely delive ... process. Experience coordinating writing activities for regulatory submissions. Good knowledge of regulatory...

  3 days ago from BioSpace

• DIRECTOR of Quality & Regulatory Affairs Medical Device FDA

  Safari Solutions On Behalf of Midmark - Dayton, OH

  Regulations) Preparation of documentation for 510 (k) regulatory submissions and approvals. Experience hiring, ... manager, management, , product testing, , R & D, FDA, regulatory affairs, veterinary, compliance, design control,...

  8 days ago from CareerBuilder

• Senior Regulatory Operations Specialist

  Ockham - King of Prussia, PA

  in the King of Prussia, PA area is looking for a Senior Regulatory Operations Specialist. This is a perm position. ... email and conference call interaction *Works with the manager to develop milestones and timelines, relays these...

  24 days ago from MiracleWorkers.com

• Senior Submission Writer / Expert Submission Writer

  Novartis Pharmaceuticals - East Hanover, NJ

  Act as liaison between clinical trial teams and document publishing and/or regulatory operations to ensure timely delive ... process. Experience coordinating writing activities for regulatory submissions. Good knowledge of regulatory...

  11 days ago from BioSpace