Roles owning submissions, agency interactions and regulatory strategy across FDA, EMA and other health authorities.
352 roles found · page 13 of 15
Medtronic · Lafayette, CO
AstraZeneca · Cambridge Kendall SQ, MA
Medtronic · Fridley, MN
Merck · North Wales (upper Gwynedd), PA +1 more
Cencora · Whitestown, IN
Thermo Fisher Scientific · Allentown, PA
Labcorp · Baltimore, MD
AstraZeneca · Gaithersburg, MD +1 more
AstraZeneca · Gaithersburg, MD +3 more
Neurocrine Biosciences · San Diego
Amgen · Cambridge Kendall SQ, MA
Gilead Sciences · Santa Monica, CA +1 more
Madrigal Pharmaceuticals · Waltham -, MA +1 more
Bristol Myers Squibb · New Brunswick, NJ +5 more
Johnson & Johnson · Spring House, PA +2 more
Globus Medical · Audubon, PA
Abbott · Plymouth, MN
Johnson & Johnson · Raritan, NJ
Edwards Lifesciences · Irvine, CA
Vertex Pharmaceuticals · Boston, MA
AstraZeneca · Gaithersburg, MD
Vertex Pharmaceuticals · Boston, MA
Zimmer Biomet · San Diego, CA
Abbott · Temecula, CA +1 more
Zimmer Biomet · Englewood, CO
Regulatory affairs is the interface between a company and the health authorities that decide whether its product reaches patients. The work spans strategy (what evidence a filing needs and when), operations (assembling and publishing submissions in eCTD format), and labelling and advertising review post-approval. Drug-side roles are framed around INDs, NDAs, BLAs and MAAs; device-side roles around 510(k), De Novo, PMA and EU MDR technical documentation — the two tracks are related but rarely interchangeable, so postings usually specify.
Roles in this area are also listed as regulatory affairs jobs, RA jobs, regulatory submissions jobs and regulatory strategy jobs.
Discover opportunities that align with your skills and goals.
A clean, modern experience that keeps you focused on what matters.
Transparent information and insights you can rely on.
Save, track, and apply with confidence — every step of the way.