Specialist - Regulatory Affairs - Plainsboro, United States - Novo Nordisk A/S

Specialist - Regulatory Affairs

3 weeks ago

**About the Department*** · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA ...

Regulatory Affairs Associate

4 days ago

Guerbet is a human-scale company that aims to become a new global leader in medical imaging. · Pioneer in contrast media with 90 years' experience, Guerbet is the only pharmaceutical group dedicated to medical imaging worldwide, with a presence in almost 80 countries via a networ ...

Manager Regulatory Affairs

1 week ago

**SUMMARY OF POSITION** · Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and submitting highest-quality regulatory submissions to the FDA within company timelines and in acco ...

Director Regulatory Affairs

1 week ago

SUMMARY OF POSITION · ORGANIZATION STRUCTURE · The Director, Regulatory Affairs reports into the VP, Regulatory Affairs and is based in Pine Brook, New Jersey. Manages team of 2-5 direct and indirect reports. · RESPONSIBILITIES · QUALIFICATIONS · - Advanced degree in a life scien ...

Manager - Regulatory Affairs - Therapeutic Area

2 days ago

**About the Department*** · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA ...

Regulatory Affairs Director

1 week ago

Are you a seasoned Regulatory Affairs professional with a passion for ensuring compliance and driving regulatory strategy in the medical device industry? · We're are on the look out for a dynamic Regulatory Affairs Director to lead regulatory initiatives for a one-of-a kind start ...

Specialist - Regulatory Affairs

2 weeks ago

About the DepartmentThe Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to prov ...

Specialist - Regulatory Affairs

3 weeks ago

About the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to ...

Specialist - Regulatory Affairs

2 weeks ago

About the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to ...

Director of Regulatory Affairs

4 weeks ago

Hybrid - 3 days a week in office - Princeton, NJ · The Associate Director of Regulatory Affairs Labeling will assist in the development of a cross-functional labeling strategy for products worldwide, including providing expert input on labeling requirements and strategic guidanc ...

Regulatory Affairs Associate

5 days ago

Apply now " · Date: Apr 30, 2024 · Location: · Princeton, NJ (USA), US · Job Type: Graduate · At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose. · We are a global leader in medical imaging, offering an extensive portfolio of p ...

director regulatory affairs

2 weeks ago

Job Description · Job DescriptionSUMMARY OF POSITION · The Director, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Clients s drug development programs, polici ...

Regulatory Affairs Associate

2 weeks ago

At Guerbet, we build lasting relationships so that to enable people to live better . This is · Our Purpose. · We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventio ...

director regulatory affairs

2 weeks ago

SUMMARY OF POSITION The Director, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Client's 's drug development programs, policies and procedures; ensuring a com ...

manager regulatory affairs

1 week ago

SUMMARY OF POSITION Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and submitting highest-quality regulatory submissions to the FDA within company timelines and in accordance ...

Regulatory Affairs Analyst

3 weeks ago

Regulatory Affairs Analyst (Master's or equiv. degree w/1 yr. exp.) Princeton, NJ. Exp. in: manage & coordinate regulatory affairs team; implement regulations for preparation & submission of regulatory documentation; risk management planning & traceability matrix; submitting docu ...

Regulatory Affairs Associate

5 days ago

Apply now " · Date: Apr 30, 2024 · Location: · Princeton, NJ (USA), US · Job Type: Graduate · At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose. · We are a global leader in medical imaging, offering an extensive portfolio of p ...

Regulatory Affairs Associate

2 weeks ago

At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose. · We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional ...

manager regulatory affairs

2 weeks ago

Job Description · Job Description · SUMMARY OF POSITION · Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and submitting highest-quality regulatory submissions to the FDA with ...

Senior Regulatory Affairs

4 days ago

Hi, · Welcome to Diverse Lynx We combine industry leading expertise and our personal dedication to help you find your next career opportunity. We are a Minority and Women Owned Business Enterprise (MWBE) certified by the State of New Jersey and Minority Business Enterprise (MBE) ...