
Regulatory Operations Submissions - various levels - US or Canada (Talent Pool)
Houston, Texas
Parexel International Corporation
Attention Senior Submissions Specialists and Regulatory Operations Submissions Managers Drive Regulatory Excellence in a Growing FSP Partnership Due to our ongoing success, we expect to be growing our North American Regulatory Operations te...
28d
Job Type | Full Time |

Regulatory Operations Submissions - various levels - US or Canada (Talent Pool)
Providence, Rhode Island
Parexel International Corporation
Attention Senior Submissions Specialists and Regulatory Operations Submissions Managers Drive Regulatory Excellence in a Growing FSP Partnership Due to our ongoing success, we expect to be growing our North American Regulatory Operations te...
28d
Job Type | Full Time |

Regulatory Operations Submissions - various levels - US or Canada (Talent Pool)
Kennesaw, Georgia
Parexel International Corporation
Attention Senior Submissions Specialists and Regulatory Operations Submissions Managers Drive Regulatory Excellence in a Growing FSP Partnership Due to our ongoing success, we expect to be growing our North American Regulatory Operations te...
28d
Job Type | Full Time |

Regulatory Operations Submissions - various levels - US or Canada (Talent Pool)
Hackensack, New Jersey
Parexel International Corporation
Attention Senior Submissions Specialists and Regulatory Operations Submissions Managers Drive Regulatory Excellence in a Growing FSP Partnership Due to our ongoing success, we expect to be growing our North American Regulatory Operations te...
28d
Job Type | Full Time |

Senior Regulatory Affairs Quality Systems Specialist
Senior Regulatory Affairs Quality Systems Specialist Job Locations US-Remote Company Meridian Bioscience, Inc. Department Quality & Regulatory Affairs # of Openings 1 About Meridian Meridian Bioscience is a fully integrated life science com...
28d
Job Type | Full Time |

Pine Brook, New Jersey
Independently authors, compiles, reviews, and schedules high-quality regulatory submissions in adherence with standards that are fully compliant with FDA and ICH requirements within company timelines. Submissions will include: ANDAs, NDAs, ...
43m
Job Type | Full Time |

Associate/Sr. Associate Regulatory Operations, CMC
Pine Brook, New Jersey
This position is primarily responsible to plan, coordinate and prepare regulatory submissions in adherence with technical document standards that are fully compliant with FDA and ICH requirements. Serve as a primary publisher of US Regulato...
43m
Job Type | Full Time |

Senior Regulatory Affairs Specialist
Austin, Texas
Description Company Overview Headquartered in suburban Atlanta, Georgia, Artivion, Inc. specializes in developing innovative medical devices aimed at addressing challenging cardiac and vascular conditions. Our Austin facility houses a diver...
28d
Job Type | Full Time |