Regulatory Affairs Specialist
Minnesota Jobs
Regulatory Affairs SpecialistMedtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a range of medical devices focusing on a diverse line of Sutures (absorbable/non-absorbable, coated/uncoated). Regulatory support will focus on sustaining globalization, international submissions, commercial support, manufacturing support, systems improvement, and other responsibilities aligned with global medical device regulations and the goals of the Wound Management business.Responsibilities may include the following and other duties may be assigned:Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and inspections.Leads or compiles all materials required in submissions, license renewal and annual registrations.Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance.Monitors and improves tracking / control systems.Keeps abreast of regulatory procedures and changes.May direct interaction with regulatory agencies on defined matters.Recommends strategies for earliest possible approvals of clinical trials applications.To be considered for this role, you must have:Bachelor's degree requiredMinimum of 2 years of relevant experience, or advanced degree with a minimum of 0 years of relevant experience.Preferred qualifications include:Experience with U.S. FDA and international regulatory requirements for medical devicesFamiliarity with EU MDR, MDD, ISO 13485, ISO 14971, and related standardsExperience supporting regulatory submissions, audits, or inspectionsStrong written and verbal communication skillsStrong organizational skills with the ability to manage multiple prioritiesExperience collaborating in a cross-functional, fast-paced environmentFamiliarity with medical device product development or lifecycle managementRAC certification or progress toward certificationExperience working with Notified Bodies or global regulatory agencies.Medtronic offers a competitive salary and flexible benefits package. A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
$60k - $120k
...Regulatory Operations Specialist IAbbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices...SuggestedFor contractorsWork experience placementWorldwideShift work- ...Socket.dev is seeking a Regulatory Affairs Specialist to support market authorizations and registrations for Scanlan products across worldwide markets. You will assist with design files, technical documentation, and product listings to ensure compliance and timely approvals...SuggestedWorldwide
$74.4k - $111.6k
...collaboration as we work together to engineer the extraordinary. This position will be based in Mounds View, MN. The Regulatory Affairs Specialist assists in the development of strategies for worldwide product registration with global regulatory agencies to...SuggestedH1bLocal areaImmediate startRemote workWorldwideFlexible hours- ...Regulatory Affairs Specialist The Regulatory Affairs Specialist will assist in maintaining market authorizations for Scanlan products, including design files, technical documentation, product registrations and listings. They will also assist with post-market surveillance...SuggestedWork experience placementWork at officeWorldwide
$74.4k - $111.6k
...collaboration as we work together to engineer the extraordinary.? This position will be based in Mounds View, MN. The Regulatory Affairs Specialist assists in the development of strategies for worldwide product registration with global regulatory agencies to...SuggestedFull timeH1bLocal areaImmediate startRemote workWorldwideFlexible hours- ...flexible on work hours, Hybrid on site Key Responsibilities Regulatory Strategy & Compliance • Develop and execute global... ...Product Introduction (NPI) • Participate as the Regulatory Affairs and Product Stewardship representative on global product development...Monday to FridayFlexible hours
$74.4k - $111.6k
...Regulatory Affairs SpecialistMedtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a range of medical devices focusing on a diverse line of Sutures (absorbable...H1bWork at officeLocal areaImmediate startFlexible hours- .... • Conduct evaluations of chemical formulations to support regulatory compliance determinations. • Administer regulatory label and... ...Policy: Skills and Requirements • 4+ years of Regulatory Affairs experience in a corporate environment • Bachelor's degree with...
- ...Regulatory Affairs Specialist This role is ideal for a regulatory professional with strong experience in FDA, Health Canada, and EU medical device requirements. The Regulatory Affairs Specialist will maintain global registrations and technical documentation, support...Work at office
- ...Senior Regulatory Affairs SpecialistWork mode: Hybrid Onsite Location(s): Marlborough, MA, US, 01752 Additional Location(s): US-CA-Irvine;... ...an enthusiastic individual for a Senior Regulatory Affairs Specialist position (hybrid work mode) supporting our rapidly growing active...Work at officeLocal areaRelocation3 days per week
- ...Principal Regulatory Affairs Specialist The Principal Regulatory Affairs Specialist is responsible for developing and implementing regulatory strategies across projects, processes, and/or products. This individual partners with internal stakeholders and external consultants...Worldwide
$80.9k - $127.05k
...US-Nationwide-FIELD Full time 20186058 What Regulatory Affairs contributes to Cardinal Health Regulatory provides regulatory affairs... ..., MA. Job Summary The Principal Regulatory Affairs Specialist supports the Medical Solutions Regulatory Affairs team by managing...Full timeTemporary workWork experience placementLocal areaImmediate startRemote workFlexible hours$107.2k - $160.8k
...font-size: 30px; font-weight: bold; width: 883px; left: 5px; height: 72px; padding-left: 17px; padding-top: 15px; } he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast’s quality system and...Work at officeLocal areaImmediate startFlexible hours- Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within the Interventional Cardiology and Vascular Therapies Division. This role is responsible for ensuring compliance with...
- ...Regulatory Affairs Specialist II - (RAS2.1) Company Description Stereotaxis is the global leader in innovative robotic technologies designed to enhance the treatment of arrhythmias and perform endovascular procedures. Its mission is the discovery, development and delivery...Work at office
- ...The Science Team at Pride Health is hiring a "Regulatory Specialist" for a top materials science company. Key Responsibilities Manage U.S. product... ...regulated products. Collaborate with global Regulatory Affairs teams to facilitate regulatory submissions and approvals. Prepare...
$85k - $95k
...Regulatory And Clinical SpecialistAs a global medtech company, we are driven by our Vision... ...course of lives.The Regulatory and Clinical Specialist will support the clinical evaluation... ...medical writing and medical device regulatory affairs or a Ph.D. with at least 3 years of...Remote workWorldwide- ...Abbott is seeking a Regulatory Affairs Specialist II to join our on-site team in Plymouth, MN. You will perform specialized analyses, prepare and review documentation for international regulatory submissions, primarily China, ensuring compliance with applicable regulations...
- ...Abbott is seeking an individual contributor to perform specialized regulatory work, ensuring products meet regulatory requirements for... ...role requires a Bachelor’s degree and experience in regulatory affairs, with strong communication and organizational skills in a fast...
- ...Pride Health’s Science Team is hiring a Regulatory Specialist for a top materials science company in Maplewood, MN. The role focuses on U.S. product registrations, regulatory documentation, and collaboration with global teams to ensure timely submissions and approvals....Hourly pay
- ...Incredible opportunity to shape global regulatory strategy and deliver breakthrough science while working from home! We’re looking for a seasoned Regulatory Project Manager who can turn strategy into action and thrive in fast-moving, innovative environments. In this...Work at officeRemote workWork from homeWorldwide
$37.91 - $56.39 per hour
This hybrid role supports DCYF compliance through advanced analytics, research design, and performance measurement. Responsibilities Independently lead the design, research, and oversight of the Compliance Division data strategy to identify and detect potential risk, fraud...Hourly payTemporary workRemote workMonday to FridayFlexible hoursShift workDay shift$35k - $48k
Junior Compliance Officer (Operations, Jr. Analyst)The MIL Corporation seeks a Junior Compliance Officer (Operations, Jr. Analyst) to support a federal law enforcement client with I-9 audit support services and worksite enforcement compliance activities. The role assists...Full timeContract workFor contractorsWork at officeRemote workWeekend work$35k - $48k
RPMGlobal is seeking a Junior Compliance Officer to aid in I-9 audit support for a federal law enforcement client in St. Paul, MN. Candidates will validate employment eligibility documentation and assist with various compliance activities. This is an on-site position requiring...- ...areas, extending our products into new geographies and high-growth adjacent markets.Under minimal supervision, the Senior Regulatory Affairs Specialist will plan, manage and implement regulatory submissions to the U.S. Food and Drug Administration (FDA), European Union...Hourly payWork experience placementWork at officeLocal areaRelocationRelocation packageShift work3 days per week
- Regulatory Affairs Consultant (Contract-to-Hire) We are seeking a Regulatory Affairs Consultant for a 6-month contract-to-hire opportunity supporting Class II medical devices, with a strong focus on SaMD. 6-month contract-to-hire 40 hours per week Hybrid: 2-3 days onsite...Contract work
- ...Abbott Laboratories in the United States seeks a Principal Regulatory Affairs Specialist to join Abbott’s Vascular Division on-site in St. Paul, MN. The role focuses on global regulatory submissions, ensuring product compliance and timely market approvals. As an experienced...
$94k - $150k
...Senior Regulatory Affairs SpecialistThe Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and authorities to secure timely product clearances. Responsibilities include coordinating and preparing regulatory submission documents for agencies...Full timeWork at officeImmediate startWork visaRelocation package3 days per week- ...focus is to revolutionize the standard of care in neuromodulation to positively impact patient’s lives. As a Principal Regulatory Affairs Specialist, you will provide Regulatory Affairs support for product development, sustaining engineering projects and compliance based...
$120.49k - $192.78k
...Principal Regulatory Affairs SpecialistJoin RespirTech's team in Plymouth, MN as a Principal Regulatory Affairs Specialist, where you will develop and execute global regulatory strategies for innovative airway clearance therapy devices, enhancing product development,...Full timeWork at officeImmediate startWork visaRelocation package3 days per week
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