Regulatory Affairs Specialist II - Electrophysiology Devices
$61.3k - $122.7kAbbott
A healthcare company is seeking a passionate Regulatory Affairs Specialist II to join their team in Plymouth, MN. In this role, you will handle regulatory submissions for Electrophysiology devices, ensuring compliance with FDA and international standards. Candidates should have a Bachelor's degree and 2-3 years of experience in a regulated industry, preferably in regulatory affairs. The position offers competitive pay ranging from $61,300.00 to $122,700.00, based on experience and location. #J-18808-Ljbffr Abbott
$61.3k - $122.7k
A global healthcare leader is seeking a Regulatory Affairs Specialist II to join their Electrophysiology team in Plymouth, MN. The role involves preparing regulatory submissions for heart disease treatment devices, reviewing documentation, and ensuring compliance with FDA...Suggested$61.3k - $122.7k
...and products in diagnostics, medical devices, nutritionals and branded generic... ...executives, and scientists.In Abbott’s Electrophysiology (EP) business, we’re advancing the... ...a passionate, experienced **Regulatory Affairs Specialist II** to join our team on-site in Plymouth...SuggestedFor contractorsWorldwideShift work$78k - $156k
...products in diagnostics, medical devices, nutritionals and branded... .... In Abbott's Electrophysiology (EP) business, we're advancing... ..., experienced Senior Regulatory Affairs Specialist to join our team on-site... ...Advanced level degree ~ Class II or Class III medical...SuggestedFor contractorsWorldwideShift work- Job Details Job Title: Regulatory Affairs Specialist II Education: Bachelor\'s Degree Location: Minneapolis, MN 55401 US (Primary) Career Level:... ...experience. 3-5 years\' experience in regulated medical device industry highly preferred. Knowledge of global Class I,...SuggestedFull timeWork at office
- ...Distribution, and Operational Excellence team, the Trade Compliance Specialist II supports compliant, accurate, and timely international... ...domestic and international rules governing shipment of medical devices, medical measuring systems, and medical disposable products....SuggestedWork at officeFlexible hours
- A leading life sciences company seeks an Advanced Regulatory Affairs Specialist to assist in regulatory submissions and ensure compliance with applicable medical device regulations. The ideal candidate will have a Bachelor's degree with relevant experience, attention to...Full time
$68.3k - $88.77k
## Quality Systems Compliance Specialist IIApplyremote type:... ...Systems Compliance Specialist II* is responsible for maintaining... ...supplier audits* Assists with regulatory submissions, registrations and... ...regulatory compliance in the medical device or related regulated field*...Work experience placement$73.6k - $110.4k
...compassionate world. A Day in the Life REGULATORY AFFAIRS SPECIALIST Onsite At Medtronic, we bring bold... ...reviewing labeling and changes to existing devices and documentation. Provide feedback... ...industry, including exposure to Class II and/or Class III medical devices (510(...Local areaWorldwideFlexible hours- ...leading global healthcare technology company is seeking a Regulatory Affairs Specialist in Minneapolis, MN to manage regulatory submissions for medical devices. The candidate should have experience in Class II and III devices and a strong understanding of FDA and EU regulations...
- A global medical technology company in Plymouth, Minnesota is looking for a Trade Compliance Specialist II. This role involves ensuring compliance with U.S. and international Customs regulations for the movement of goods. Candidates should have a Bachelor's degree and 5...Work at office
$74.4k - $111.6k
## Regulatory Affairs Specialist -NeuroApplyremote type: Onsitelocations: Minneapolis, Minnesota, United States... ...labeling and changes to existing devices and documentation.* Provide feedback and... ...industry, including exposure to Class II and/or Class III medical devices (510(...H1bLocal areaWorldwideFlexible hours- ...Senior Regulatory Affairs Specialist Work mode: Hybrid Onsite Location(s): Marlborough, MA, US, 01752 Additional Location(s): US-CA-Irvine; US... ...work mode) supporting our rapidly growing active implantable device portfolio. This role will be responsible for Regulatory...Hourly payWork at officeLocal areaRelocationShift work3 days per week
$94k - $150k
...Senior Regulatory Affairs Specialist, Ultrasound The Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and... ...Technical Files, Declarations of Conformity, and Medical Device Licenses—for various global markets. Support cross-functional...Full timeWork at officeLocal areaWork visaRelocation package3 days per week$110k - $160k
...SYSTEMS Inspire is the first of its kind medical device designed to make a difference in the lives of those living... ..., come be a part of our great team! The Senior Regulatory Affairs Specialist will lead and execute regulatory strategy for an implantable...Work experience placementLocal areaFlexible hours$113.03k - $165.77k
...job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory approvals... ...Minimum Experience: 7+ years of US and International medical device regulatory submission/approval experience, to include FDA, MDD,...Immediate start$62.3k - $102.35k
...$62,300.00 - $102,350.00 Position Summary Responsible for regulatory affairs activities to assist in regulatory submission, annual reports... ...registrations, and listings. Assure compliance with applicable medical device regulations per jurisdiction, guidance, and standards. Assist...Temporary workInternshipWorldwideFlexible hours- The University of Minnesota is hiring a Regulatory Specialist 1 or 2 in Saint Paul, MN. This full-time position involves managing regulatory documentation for clinical trials, ensuring compliance with federal regulations, and collaborating with research teams. The role...Full timeWork at office
$77.2k - $94.5k
The Regulatory Affairs Specialist is responsible for ensuring comprehensive compliance with regulatory requirements throughout the entire product... ...regulations Author global submissions for Class I-IV medical devices, and prescription drugs globally, which includes (but not...- Medtronic plc in Minneapolis is seeking a passionate Regulatory Affairs Specialist to support regulatory submissions for both the Americas and the... ...in a scientific discipline and at least 2 years of medical device regulatory experience. Join Medtronic to make a meaningful...
$92k - $138k
Job Overview Senior Regulatory Affairs Specialist (Global Markets - High Risk Devices) - Neuromodulation. The role develops global regulatory strategies and leads worldwide submissions for high‑risk medical devices. Responsibilities include managing strategy meetings, submissions...Temporary workWork at officeLocal areaWorldwideFlexible hours- ...biotechnology firm in Minneapolis is seeking a professional for a regulatory affairs role. The position involves assisting with regulatory... ...submissions, maintaining regulatory files, and compliance with medical device regulations. Candidates must possess a Bachelor's degree with...
$30 - $37 per hour
...Job Title: Regulatory Compliance Specialist Job Description This role supports the Regulatory Compliance team by assisting in maintaining... ...System (QMS) and meet regulatory requirements for medical devices. Responsibilities Maintain accurate and complete...Contract workTemporary workMonday to Friday$68k - $136k
...with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues... ..., and maintenance of the quality management system to ensure regulatory compliance and product quality. The position provides hands-on...For contractorsWork experience placementWorldwideShift work- ...UPON AWARDING OF GOVERNMENT CONTRACT******** Credentialing Specialists will provide credentialing service and support to operate IRS credentialing... ...online credentialing training and maintain compliance with PIV-II SmartID credential requirements. Knowledge of ICAM and...Full timeContract workTemporary workFor contractorsLocal areaRelocationShift workNight shiftWeekend work
$65k - $70k
...dedicated Affordable Housing Compliance Specialist. This role directly supports our mission... ...will consist of a thorough review of all regulatory compliance records in accordance with... ...standards Assists Compliance Specialist II & III with lease‑up activities of new sites...Temporary workWork at officeLocal areaRemote workShift work1 day per week- Senior Regulatory Affairs Associate - Medical Device We are partnering with an innovative medical device company seeking a Senior Regulatory Affairs Associate to support regulatory strategy and submissions for new and existing products. This individual will work closely...
- ...Job Description Job Description A medical device client is hiring a permeant Sr. Regulatory Specialist, onsite in Maple Grove, MN. This person will assist with medical writing (including preparation and/or finalization of test reports), regulatory filings, review...Work at office
- Job Title Regulatory Specialist 1 or 2 (Research Professional 1 or 2) Job Class: 8351RF or 8352RF... ...Research Professional 1 or 2 - Regulatory Affairs Specialist Working Title: Regulatory... ...New Drug (IND) and/or Investigational Device Exemption (IDE) applications. 2....Work experience placementInterim roleWork at officeLocal areaRemote workFlexible hours3 days per week
- ...specialize in developing at‑home therapy devices to treat lymphedema, chronic venous... ...respiratory illnesses. The Compliance Specialist is responsible for supporting the development... ...external and internal compliance, payer and regulatory audits, reviews, attestations and...Hourly pay
$102.1k
...our employees experience every day. The Principal Regulatory Affairs Specialist is responsible for planning, managing and implementing... ...regulatory strategies and prepare submissions for Class II medical devices. ● Create innovative regulatory pathways that support...Hourly payWork at officeLocal areaWorldwideShift work3 days per week
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