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Kelly Services
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Plymouth, Minnesota
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Job Title: Regulatory Affairs Specialist
Location: Plymouth, MN (Hybrid: 3 days onsite ... Regulatory Affairs Specialist to join our dynamic team in Plymouth, MN. This is a hybrid role, providing the
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Actalent
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Minneapolis, Minnesota
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Senior Regulatory Affairs Specialist
Job Duties:
Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements
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Boston Scientific
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Maple Grove, Minnesota
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Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II, LAAC - IC About the role: At ... Specialist II position (hybrid work mode) supporting our rapidly growing Left Atrial Appendage Closure (LAAC
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Boston Scientific
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Maple Grove, Minnesota
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Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II, LAAC - IC About the role: At ... Specialist II position (hybrid work mode) supporting our rapidly growing Left Atrial Appendage Closure (LAAC
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Boston Scientific
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Maple Grove, Minnesota
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Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II, LAAC - IC About the role: At ... Specialist II position (hybrid work mode) supporting our rapidly growing Left Atrial Appendage Closure (LAAC
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Boston Scientific
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Arden Hills, Minnesota
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supervision, the Regulatory Affairs Specialist II is responsible for planning, managing, and implementing ... is also responsible for ensuring continued compliance with regulatory agency approvals. Your
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Boston Scientific
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Maple Grove, Minnesota
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Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II About the role: At Boston ... will continue to make an investment in Peripheral Interventional treatments. The Specialist II is
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Actalent
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Saint Paul, Minnesota
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Job Title: Sr. Regulatory Affairs Specialist
Job Description
Responsibilities Include ... , compliance test requirements, and clarification/follow-up of submissions under review.
Provide technical
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Boston Scientific
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Maple Grove, Minnesota
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Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II About the role: At Boston ... will continue to make an investment in Peripheral Interventional treatments. The Specialist II is
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Boston Scientific
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Maple Grove, Minnesota
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Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II About the role: At Boston ... will continue to make an investment in Peripheral Interventional treatments. The Specialist II is
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Boston Scientific
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Maple Grove, Minnesota
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Recruiter: Spencer Gregory Hale Sr. Regulatory Affairs Specialist About the role: At Boston ... in Interventional treatments. The Senior Regulatory Affairs Specialist will provide regulatory
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ACIST Medical Systems
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Eden Prairie, Minnesota
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Regulatory Affairs Specialist II LinkedIn Twitter Email Message Share Why Join Bracco Medical ... Regulatory Affairs Specialist II completes regulatory submissions related to market expansions as well as
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Boston Scientific
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Arden Hills, Minnesota
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indications. With adequate supervision, the Regulatory Affairs Specialist II is responsible for planning ... world-wide product registrations. The position is also responsible for ensuring continued compliance
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Randstad US
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minneapolis, Minnesota
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regulatory affairs specialist ii.
minneapolis , minnesota
posted september 6, 2024 ... Affairs function eg; compliance to 21 CFR 820,807,803 ISO 13485 requirements, Company policies, operating
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Teleflex
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Maple Grove, Minnesota
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Regulatory Affairs Specialist
Date: Sep 14, 2024
Location: Maple Grove, MN ... .
Position Summary
The Regulatory Affairs Specialist will develop strategies, submissions, and
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Bio-Techne
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Minneapolis, Minnesota
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The Advanced Regulatory Affairs Specialist provides independent support to senior regulatory staff to ... handling and hazards, compliance, and proper use of equipment.
Performs additional duties as assigned
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Integer
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Plymouth, Minnesota
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States and International markets and ensure compliance with relevant US, EU, ISO standards and other ... . * Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance
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Teleflex
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Maple Grove, Minnesota
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Sr. Regulatory Affairs Specialist
Date: Sep 23, 2024
Location: Maple Grove ... program manager.
• Ensure compliance with design controls and good manufacturing practices.
• Apply
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Medtronic
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Minneapolis, Minnesota
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lifecycle. The Sr Principal Specialist has primary responsibility for compliance with US and EU regulatory ... and Class III medical devices. The Sr Principal Regulatory Affairs Specialist is responsible for
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Boston Scientific
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Arden Hills, Minnesota
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Recruiter: Spencer Gregory Hale Principal Regulatory Affairs Specialist About the role: The ... compliance in the areas of Medical Electrical Equipment, Material Controls, Supplier Quality, and others
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Inspire Medical Systems Inc.
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Golden Valley, Minnesota
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Specialist provides regulatory support for implantable neurostimulation therapy for the treatment of ... reviewers to answer questions. Review labeling and promotional material for regulatory compliance. Required
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Vital Images Inc
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Minnetonka, Minnesota
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further! We are looking for a savvy and passionate Senior Regulatory Affairs Specialist to join our team ... ensure compliance with U.S. requirements. Organizing pre-sub meetings with FDA. Generate and submit HIT
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Philips
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Plymouth, Minnesota
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The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive ... level
Provide guidance on global compliance such as CE Marking and product registrations, clinical
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Abbott
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Plymouth, Minnesota
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Senior Regulatory Affairs Specialist to join our team on-site in Plymouth, or St. Paul, MN. In this ... appropriate personnel.
Reviews device labeling for compliance with FDA submissions and applicable
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Abbott
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St. Paul, Minnesota
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Affairs Specialist** to join our team on-site in St. Paul, MN.This new team member will provide support ... . Participate in risk-benefit analysis for regulatory compliance.
Monitor impact of changing regulations on
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Medtronic
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Minneapolis, Minnesota
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The Senior Regulatory Affairs Specialist develops strategies for worldwide product registration ... specialist also assists with the license maintenance including renewals, design/manufacturing change
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US Electronics
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Minneapolis, Minnesota
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compliance & regulatory authorities. Skills required: EU MDR, ISO 13485, cGmp, IQ/OQ/PQ, MDSAP, 93/42 EEC
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Bausch + Lomb
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Saint Paul, Minnesota
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Authority queries throughout the product lifecycle. Responsible for regulatory compliance and change management. Responsible for regulatory compliance, regulatory intelligence surveillance and US regulatory
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