Average salary: $76,439 /yearly
More statsSearch Results: 2,895 vacancies
...workforce-led resource groups.
From discovery to delivery, come help us shape the future of medicine.
Description
The Regulatory Affairs Specialist reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate...
Suggested
Hourly pay
Holiday work
Part time
Local area
Flexible hours
...Job Description:
Principal Scientist- Scientific & Regulatory Affairs
The Principal Scientist provides regional scientific and regulatory expertise and leverages scientific networks to enable the development and execution of Mars Wrigley (MW) Scientific and Regulatory...
Suggested
Seasonal work
...Canada. Leading a small team, this is for somebody with prior Regulatory management experience and knowledge of IVD requirements.... ...regulatory standards.
Experience Required
~6 years' Regulatory Affairs experience within Medical Devices or IVDs, understanding FDA...
Suggested
3 days per week
...Are you a skilled Regulatory Affairs Manager with experience in combination products seeking your next career move in Chicago? We're excited to offer a direct placement opportunity for our client!
Responsibilities
Lead Quality and Regulatory Services Initiatives:...
Suggested
Permanent employment
Temporary work
Remote job
...devices for different application areas, from services, design to large scale manufacturing.
Job Description
Lead Quality and Regulatory Services Initiatives: Manage aspects of combination product programs and projects, coordinating with both internal teams and...
Suggested
Remote job
Worldwide
2 days per week
...The Regulatory Affairs Specialist will be the regulatory representative for assigned due diligences, under the direction of the Global Regulatory Strategy Lead (GRSL).
An external company and assets or individual assets alone can be the subject of due diligence....
Suggested
Contract work
...for more information, and follow on Twitter and LinkedIn.
Job Description
Opportunity at a Glance
The Senior Regulatory Affairs Analyst is responsible for interpreting statutes, regulations and administrative rules of various issuing bodies and...
Suggested
Holiday work
Full time
Flexible hours
...please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description
The Manager, Regulatory Affairs In Vitro Diagnostics and Companion Diagnostics works with internal and external partners to develop and implement global...
Suggested
Remote job
Holiday work
Temporary work
Local area
...LinkedIn.
Job Description
The Associate Director, RA Global Regulatory Strategy, US & Canada (Oncology) is responsible for the... ...regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial....
Suggested
Holiday work
Temporary work
Local area
...worked to support the passage of numerous bills that have benefitted close to 500 million people in developing countries. Political Affairs Internship: The role focuses on making poverty a focus of U.S., Canadian and U.K. foreign policy. This is a part-time 12-hours per...
Suggested
Part time
Internship
Remote job
...Overview
The Regulatory Publishing Specialist is responsible for the formatting, publishing (PDF), eCTD compilation, review, and dispatch... ...Specialist will work collaboratively with the Regulatory Affairs team along with project teams and other functional areas to ensure...
Suggested
Local area
Night shift
Weekend work
Afternoon shift
3 days per week
Position Title: Regulatory Affairs Specialist
Position Type: Regular - Full-Time
Position Location: Oakbrook Terrace
Requisition ID: 28326
The Regulatory Affairs Specialist is responsible for product composition and label regulatory...
Suggested
Full time
Work alone
...The Senior Manager, Regulatory Affairs Advertising & Promotion is responsible for directing the regulatory aspects of internal and external communications including advertising and promotional activities. They will coordinate the development and implementation of regulatory...
Suggested
Full time
Night shift
Weekend work
Afternoon shift
3 days per week
...Director, Regulatory Affairs
About the Company
Globally recognized biotechnology company
Industry
Biotechnology
Type
Privately Held
About the Role
The Director, Regulatory Affairs will be responsible for developing global regulatory strategies,...
Suggested
Remote job
...Senior Director, Regulatory Affairs
About the Company
International labelling organization based in Los Angeles
Industry
Retail
Type
Privately Held
About the Role
The Senior Director, Regulatory Affairs will be responsible for developing and managing...
Suggested
Remote job
Worldwide
...Job Description
Title: Regulatory Specialist
Location: Skokie, IL
Overview:
Sterling has helped build careers for thousands for professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company,...
Work experience placement
...by offering high quality confections and snacks while maintaining an unrelenting commitment to excellence.
ROLE SUMMARY
The Regulatory Specialist is responsible for supporting both internal partners and external customers as it pertains to regulatory functionality...
Full time
Work experience placement
Remote job
Shift work
Day shift
Job Type
Full-time
Description
Reporting to the Food Safety, Quality, and Regulatory Manager, the Regulatory Compliance Specialist is responsible for maintaining the effective and consistent operation, verification, and current compliance of our organization's...
Full time
...Job Description
This position reports directly to the Global Product Regulatory Compliance Program Manager and is responsible for ensuring that all John Crane products are compliant with applicable product regulatory compliance requirements. Additionally, this position...
Location: Chicago, IL Job Description:
Regulatory Affairs Managers handle all regulatory functions for a large portfolio of studies.Â
This includes Institutional Review Board (IRB) approval, all specialty subcommittee reviews, and FDA IND and IDE submission....