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...'re currently seeking a dynamic and experienced Project Manager (Medical Device Regulatory). The role can be offered as a full time or part time opportunity... ...and meeting project deadlines.
Evaluate and authorize changes affecting project scope, budget, or timeline.
Lead...
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...Aesthetics on LinkedIn.
Job Description
Description
The Manager Regulatory Affairs represents US regulatory affairs for device... ...with the commercial needs.
+ Communicates planned/approved changes with operations, commercial, medical affairs, and marketing....
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...superior customer experience. We’re actively seeking a talented Change Consultant to join our Enterprise Change Enablement team in... ...sponsors.
Influence the implementation of the full change management strategy and plans.
Partner with Internal...
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...Ekman Associates, Inc. is a management consulting firm that specializes in developing business, digital, and technology strategy, delivering... ...for a Workday migration initiative focusing on communication, change management and training.
Key Skills:
•Workday Experience -...
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Manager, Regulatory Affairs - Biosense Webster, Inc. - (***) ***-****W
Description
Biosense Webster, part of the Johnson & Johnson MedTech family, is currently recruiting for a
Manager, Regulatory Affairs
.
This role will work a Flex/Hybrid schedule and must be located within...
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...Aesthetics on LinkedIn.
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Description
The Sr Manager Regulatory Affairs represents US regulatory affairs for device... ...aligned with the commercial needs.
Communicates planned/approved changes with operations, commercial, medical affairs, and marketing....
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...procedures (SOPs) are adhered to; recommends changes to workflow.
Creates and updates SOPs... ...business needs require at direction of management.
Education and Experience:... ...Reports.
Knowledge of US and international regulatory requirements pertaining to medical devices...
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...Description:
Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessment in Have working knowledge in US and EU medical device submissions Have experience supporting internal and external inspections Work cross-functionally and in a matrixed...
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...Job Title: Regulatory Affairs Specialist
Job Responsibilities:
This position is responsible for providing guidance... ...process for all marketed devices and implementation of changes to risk management process as needed.
Monitors proposed and current US...
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...every unique eye.
OVERVIEW:
Reporting to the SVP, Clinical and Regulatory Affairs, the Director, Regulatory Affairs will collaborate in... ...individual innovation and creativity.
•Solid project management skills to handle multiple projects and set/manage timelines with...
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$100k - $140k
...If you are a Regulatory Affairs professional with a track record in Medical Devices, please read on!
Job Title: Regulatory Manager
Location: Laguna Hills, CA
Salary: $100-140k... ...and Design History Files.
- Review changes to Existing Products, SOPs, DOPs, Test...
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...multiple regions across the U.S. Our diverse management team has many decades of experience in... ...to join our team as Senior Manager of Regulatory Compliance to support NERC and regional... ...organization is proactively addressing any changes or updates. Additionally, the manager...
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...Job Description
Job Description REMOTE – Regulatory Project Manager
Part-time - 15 hrs / week
Location; Remote, US
JOB DESCRIPTION
We are looking for an experienced Regulatory Project Manager to support the execution of regulatory strategies within...
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...Regulatory Affairs Specialist Career Opportunity Job Title Regulatory Affairs Specialist FLSA Salaried Exempt Department Regulatory... ...process for all marketed devices and implementation of changes to risk management process as needed. Monitors proposed and current US and EU...
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...are seeking an experienced Director of Regulatory Affairs to join our team at SpyGlass Pharma... ..., participating in discussions with management and providing strategic regulatory guidance... ...).
Stay abreast of regulatory trends, changes, and requirements in the pharmaceutical...
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...medical device company, has an immediate opening for a Senior Regulatory Affairs Specialist responsible for implementing regulatory strategies... ...relationship skills including negotiating and relationship management
Ability to apply sound judgment when making decisions and...
Immediate start
Home office
...and organized leader to guide and develop global clinical and regulatory activities for pre- and post-approval pediatric cardiovascular... ...regulatory guidelines, leading all regulatory submissions, and managing resources to execute clinical trials. This candidate will work...
Work experience placement
...equivalent practical experience.
2 years of experience in consumer electronics field or equivalent and 5 years of experience in regulatory compliance design, testing and certifications.
Experience with safety certification (e.g. IEC 60950-1)
Experience with safety hazard...
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We're looking for a Regulatory Affairs Associate , working in Biotechnology/Medical Devices industry in 100 Abbott Park Road... ...study protocols/reports.
Review and approval of manufacturing changes for Class III implantable medical devices.
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...Reporting to the SVP, Clinical and Regulatory Affairs, the Director, Regulatory Compliance... ...through the review and assessment of product changes for impact on regulatory filings... ..., QA, QC and R&D departments and senior management as required.
•Maintain/submit facility...
Worldwide