The Principal Regulatory Specialist is responsible for carrying out Pre-Market and Post-Market regulatory activities in compliance with Digital Factory's Quality Management System for domestic and various international markets for SaMD products. Conceive of and Implement the Regulatory Strategy in ...
Press Tab to Move to Skip to Content LinkSelect how often (in days) to receive an alert: Create AlertPrincipal Regulatory Affairs Specialist - Endoscopy Onsite Location(s): Marlborough, MA, US, 01752Additional Locations: N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - Hi...
Principal Regulatory Affairs Specialist - EndoscopyAbout the role:At Boston Scientific, this is a place where you can find meaningful purpose, improving lives through your life's work. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new busine...
Principal Regulatory Affairs Specialist - Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on develo...
Principal Regulatory Affairs Specialist - Endoscopy. Principal Regulatory Affairs Specialist – Endoscopy . This role in Regulatory Affairs will be responsible fordeveloping regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contrac...
Regulatory Affairs (RA) Specialist?. Regulatory Affairs (RA) Specialist who wants to grow your skills and take the lead on U. You will report to the SVP, Global QA, RA & ESG and work closely with colleagues from R&D, Product Management & Marketing, QA&RA and other functions, to plan ...
The Specialist, I - Regulatory Affairs will support the maintenance of EU MDR technical documentation and conduct other elements of sustaining Regulatory Affairs including maintaining “state of the art”. In addition, this position will support the regulatory department by maintaining data within reg...
Regulatory Affairs (RA) Specialist?. Regulatory Affairs (RA) Specialist who wants to grow your skills and take the lead on U. You will report to the SVP, Global QA, RA & ESG and work closely with colleagues from R&D, Product Management & Marketing, QA&RA and other functions, to plan ...
Principal Regulatory Affairs Specialist – Endoscopy . This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on devel...
The Regulatory Affairs Specialist will work closely with the Director of Regulatory Affairs to obtain and maintain global regulatory approvals to allow IPG to market its state of the art devices worldwide. Regulatory affairs experience in generating applications and experience in collaboration with ...
The Specialist, I - Regulatory Affairs will support the maintenance of EU MDR technical documentation and conduct other elements of sustaining Regulatory Affairs including maintaining “state of the art”. In addition, this position will support the regulatory department by maintaining data within reg...
The newly founded LGBTQ Health Center of Excellence seeks a highly motivated individual to join the organization in the Senior Program Manager role to serve as the Executive Director. From academic faculty and trainees to research/program staff and administrative professionals, no matter the positio...
The Director of Quality Assurance and Regulatory Affairs (QA/RA) is responsible for ensuring that Precision Optics Corporation's products meet applicable regulatory requirements and quality standards. Responsible for all quality assurance and regulatory functions across POC's Portland & Gardner site...
Supports the Acquisition Program Manager (APM) in assessing what programs are within schedule and cost baselines. The NC3 Directorate's mission is to provide support to the Program Executive Office (PEO), the Deputy Director, Deputy AFPEO NC3, and staff for acquisition and administrative control of ...
We are seeking an experienced Regulatory Generalist to join our FSP team as a Senior Regulatory Affairs Associate / Regulatory Affairs Consultant to work closely with one large, dedicated client and provide operational support in the IND/NDA maintenance stage. Associate / Consultant will also provid...
Knowledge of support activities that assist the program manager in assessing what programs are within schedule and cost baselines, be able to recommend viable solutions to problems and the pursuit of alternative courses of action. The Air Force Program Execution Office for PEO Digital (AFPEO/HB) has...
ServiceMaster Dynamic Cleaning is seeking an experienced, motivated restoration project manager to oversee water, fire, and mold remediation jobs from start to finish. ...
Senior Mechanical Project Manager Position Summary. Provide overall project management and direction for mechanical construction projects of 10 million or more. Supervise Project Superintendent and other RH White employees and subcontractors assigned to the project. Plan, organize and staff key fiel...
Commercial Project Management of Ground Up and Fit-out projects. Manage 3-4 projects at a time with supervisors on each project. Visit project sites for troubleshooting and for the purposes of ensuring project quality. Construction Project Management. ...
Provides leadership to the Regulatory labeling team in the creation and maintenance of global product labeling components. Supply Chain, Operations, Commercial and Clinical, providing regulatory guidance to aid in the preparation and submission of global product labeling materials. Employs a current...
Preclinical, Clinical, Medical Affairs, Manufacturing and Quality Control, providing regulatory guidance to aid in preparing, reviewing, and approving of regulatory NDA/IND/CTA/IMPD submissions materials. Manages a range of concurrent regulatory projects, and issues, and responds timely to ensure re...
The Environmental Compliance Specialist is responsible for helping maintain a complex, multifaceted environmental compliance program at all company-owned and/or operated assets nationwide. Environmental Compliance Specialist. The Environmental Compliance Specialist must be a strategic thinker with a...
Preclinical, Clinical, Medical Affairs, Manufacturing and Quality Control, providing regulatory guidance to aid in preparing, reviewing, and approving of regulatory NDA/IND/CTA/IMPD submissions materials. Manages a range of concurrent regulatory projects, and issues, and responds timely to ensure re...
Provides leadership to the Regulatory labeling team in the creation and maintenance of global product labeling components. Supply Chain, Operations, Commercial and Clinical, providing regulatory guidance to aid in the preparation and submission of global product labeling materials. Employs a current...
As a Trade Compliance Analyst, you will play a key role in ensuring our company's compliance with global customs authorities and facilitating day-to-day trade compliance activities. Are you an enthusiastic professional looking to expand your experience or start a career in Trade and Compliance? Rand...