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...Job Description - Regulatory Affairs Coordinator I (3285805)
Regulatory Affairs Coordinator I - ( 3285805 )
The Alzheimers Clinical and Translational Research Unit (ACTRU) is a unique group at Massachusetts General Hospital focused on early-stage interventional...
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...Regulatory Affairs Specialist
Location: Marlborough, Massachusetts
Do you have a proven track record of working with Regulations and the implementation of labeling for Medical Device UDI project? Do you want to work on a fantastic team as they undergo the changes...
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...medicines to patients through looking at and treating disease in a revolutionary way?
What if you could be the first hire in Regulatory Affairs with the opportunity to build a strategy and your team as we expand our clinical pipeline?
What this position is all about:...
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3 days per week
...and procedures, to ensure the rapid and successful development and registration of products while maintaining compliance with all regulatory requirements and commitments. Evaluates proposed regulations and advises on impact of such regulations on the company; may...
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...employees are recognized and career growth is supported.
To continue our success, we currently have an exciting opportunity for a Regulatory Affairs Specialist. This role is responsible for ensuring the regulatory compliance of all food products, including innovation...
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...in which human potential is no longer hindered by the burden of disease.
Description:
Reporting to the Sr. Director of Regulatory Affairs and Policy, this role will support and lead activities within the Regulatory group to advance development of the assets in Wave...
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...have you in front of a live recruiter.
The Opportunity
Description
We're looking for an Associate Director of Regulatory Affairs , working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States .
Works...
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Job TitlePrincipal Regulatory Affairs SpecialistJob DescriptionPrincipal Regulatory Affairs Specialist- Software & Artificial Intelligence (U.S. Hub Based)The Principal Regulatory Affairs Specialist- SW & AI will shape, lead and execute innovative regulatory strategies...
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...Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory Affairs Specialist. Remote work options may be considered on a case-by-case basis and if approved by the Company
Abiomed, part of Johnson & Johnson MedTech, is a leading provider of...
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...renewal activities for IL-labeled products. Related duties include participation on design and risk management teams, initiation of regulatory plans for both new products and significant product modifications, documentation of regulatory impact from device modifications,...
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...The Director of Regulatory & Quality Affairs will be a critical team member supporting MDC's regulatory and quality affairs business and support client RA/QA strategy and regulatory submissions. The primary role and responsibilities include managing RA/QA business and...
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...Title:
Director, Global Regulatory Affairs, Oncology
Company:
Ipsen Bioscience, Inc.
Job Description:
Director, Global Regulatory Affairs, Oncology
Summary / purpose of the position
To be accountable for the strategy, tactics and implementation of...
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...make investments in Endoscopy treatments, both within established product lines as well as in future pipelines.
The Senior Regulatory Affairs Specialist will provide regulatory support on a range of Endoscopy devices and activities which include new product...
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...Responsibilities:
Prepares regulatory strategies and maintains submissions for U.S. and International markets, including but... ...Minimum 5 years of experience in medical device Regulatory Affairs with RAC certification or 3 years of experience w/o certification...
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...Senior Director, Regulatory Affairs
Dragonfly Therapeutics is seeking a Senior Director, reporting directly to the Senior Vice President, Head of Regulatory Affairs, to join the regulatory team within our Regulatory Affairs organization. The primary responsibility...
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...Nova Biomedical is hiring a Regulatory Affairs Specialist (Level II or Senior Level) in our Waltham, MA facility (Hybrid) to focus on assuring company compliance to US 510k, Health Canada Licensing, International Device Submissions, Licensing and Registration requirements...
...boundaries of what is possible in order to bring life-changing therapies to patients worldwide.
Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program leadership and develop CMC regulatory strategy for global vaccine programs in...
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...have you in front of a live recruiter.
The Opportunity
Description
We're looking for an Associate Director Regulatory Affairs CMC , working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States .
Leads development...
...Description:
The Regulatory Affairs Specialist is responsible for identifying, evaluating, and ensuring compliance with all applicable laws, regulations, and standards. The Regulatory Affairs Specialist shall also conduct reviews of all and all future target markets...
...#ForeverCaring and you will do the same.
Job Summary:
The primary responsibilities of the position are to drive improvements in regulatory affairs processes, systems and infrastructure whilst supporting regulatory strategy and registration across global markets across the...
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