Average salary: $73,394 /yearly
More stats ...with employees in multiple regions across the U.S. Our diverse management team has many decades of experience in the renewable energy,... ...and energetic candidates to join our team as Senior Manager of Regulatory Compliance to support NERC and regional Balancing Authority compliance...
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We'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. If you're a results-driven professional looking to make a meaningful impact every day, this is the place for...
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...a fast-growing commercial insurance company, has a need for a Manager, Managed Care Filings in one of our offices in FL, TX, NY, CA,... ...treatment services processed in UR.
* Serve as the liaison with regulatory and accrediting agencies for managed care UR filings.
*...
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...Job Description
Job Description Job Title: Regulatory Affairs AnalystLocation: 1125 Trenton-Harbourton Rd, Titusville, NJ 08560 920 Route 202 South, Raritan, NJ 08869, RemoteDuration: 12 MonthsSalary: $ 45/hr. (all inclusive) Job Type: W2, Temporary, Contract, Corp...
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...with a personal touch. For more information, visit Follow Allergan Aesthetics on LinkedIn.
Job Description
Description
The Sr Manager Regulatory Affairs represents US regulatory affairs for device development projects. Responsible for development, communication, and...
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...Regulatory Affairs Specialist Career Opportunity Job Title Regulatory Affairs Specialist FLSA Salaried Exempt Department Regulatory Reports... ...all marketed devices and implementation of changes to risk management process as needed. Monitors proposed and current US and EU...
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...to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex... ...and development issues
Advancing complex situations to management for guidance and training opportunities
You will prepare and...
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...duties and projects as business needs require at direction of management.
Education and Experience:
Bachelor's degree required.... ...Market Surveillance Reports.
Knowledge of US and international regulatory requirements pertaining to medical devices preferred....
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summary Looking for a Regulatory Associate within Manufacturing $18- $23 Monday through Friday 8am- 430pm JOB DUTIES AND RESPONSIBILITIES... ...skills with different computer software such as database management, spreadsheets, project management- including MS Word, Excel and...
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This is a rare opportunity to join the global regulatory team of an innovative, fast-paced, medical device company. The Company values... ...and ISO requirements as they apply.
May support some Quality Management Functions, as needed.
Qualifications & Skills: B.S. Degree in...
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...touch. For more information, visit Follow Allergan Aesthetics on LinkedIn.
Job Description
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The Manager Regulatory Affairs represents US regulatory affairs for device development projects. Executes US regulatory strategic plans and provides...
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Established aerospace manufacturing facility in Brea, CA is hiring an experienced Director of Regulatory Compliance to join their growing team.
In this role, you will oversee quality management, trade controls, ITAR compliance, and other government regulations. You will lead a...
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0-2 years of experience in regulatory affairs, and/or experience in QA, R&D, Manufacturing or Project Management within the IVD industry
Working knowledge of FDA, and CE marking requirements for IVD products is a plus
Able to work independently and with others
Able to work...
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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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...timeline.
Duties and Responsibilities:
1. Respond to regulator complaints accurately, thoroughly and timely. Identify potential regulatory risks while responding to complaints, formulate recommendations and escalate internally, as needed. Function as point of contact...
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...will be responsible for all international registration. They will come in as a level 3, so they need to have at least 5-7 years of regulatory experience. They will be supporting EUMDR and need to understand all standard regulatory documents such as CFG, CFS, and CEO....
Flexible hours
2 days per week
3 days per week
Description:
Key Responsibilities:
Create regulatory submissions (exercising judgment to protect proprietary information) for finalization... ...requirements and development issues, and/or reporting to management.
Participate in providing guidance and feedback to business unit...
...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...
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...Job Title: Regulatory Affairs Specialist
Job Responsibilities:
This position is responsible for providing guidance... ...for all marketed devices and implementation of changes to risk management process as needed.
Monitors proposed and current US and EU...
...registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.
Maintains company registrations and device listings in... ...duties and projects as business needs require at direction of management.
Education and Experience: Bachelor's degree in related field...
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