Regulatory Specialist
$27 - $40 per hourPRIDE Health
Pay rate: $27—40/Hr. (Based on Experience) Work Location On-site 4 days per week at Maplewood, MN. Position Summary: Job Description Primary Responsibilities (include but are not limited to the following): Interacting with global regulatory affairs personnel to facilitate registering or re-registering medical devices or cosmetics. Certificates may need to be notarized, apostilled, or authenticated. Individual may become a notary to carry out job duties. Support UDI database maintenance. Support regulatory trade compliance. Your Skills and Expertise Bachelor's degree or higher (completed and verified prior to start) from an accredited institution. 1–2 years of regulatory affairs experience in a private, public, government, or military environment. Additional Qualifications That Could Help You Succeed in This Role Certified Regulatory Affairs professional (RAC). Advanced degree in a scientific discipline. Experience with regulatory strategy. Experience with electronic systems (e.g., SAP, data acquisition systems, regulatory databases, UDI systems). Strong communication and collaboration skills. BENEFITS DISCLOSURE: Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - offer eligible employees comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors. Pride Global and its affiliates, including Russell Tobin, Pride Health, Pride Now, and Pride One, offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance and employee discounts with preferred vendors. Pride Global and its affiliates are an equal opportunity employer. We do not discriminate on the basis of the race, religious creed, color, national origin, ancestry, physical disability, mental disability, reproductive health decision making, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, age, sexual orientation, veteran or military status, or any other characteristic protected by applicable federal, state, or local law. Pride Global and its affiliates are a Fair Chance employer. We consider all qualified applicants, including those with criminal histories, in a manner consistent with applicable state and local Fair Chance laws and ordinances, including, the California Fair Chance Act and all applicable local Fair Chance ordinances. Accommodations We are committed to providing reasonable accommodations to applicants and employees with disabilities. If you require reasonable accommodation to participate in the application or interview process, or to perform the essential functions of this role, please contact us. Only applicable for San Francisco Candidates: Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of lactation accommodation rights, and this notice will automatically be given upon hiring, any inquiry of parental leave or lactation accommodation. #J-18808-Ljbffr
$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
- ...application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Regulatory Affairs Specialist Regular Full-Time Scanlan International, Inc., St. Paul, MN, US The Regulatory Affairs Specialist will assist in...SuggestedFull timeWork experience placementWork at officeWorldwide
- ...portfolio during new product introduction and change management processes. • Conduct evaluations of chemical formulations to support regulatory compliance determinations. • Administer regulatory label and claims review processes. • Review supplier documentation,...Suggested
$74.4k - $111.6k
...Regulatory Affairs Specialist Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first...SuggestedH1bLocal areaImmediate startRemote workWorldwideFlexible hours$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...Full timeH1bLocal areaImmediate startRemote workWorldwideFlexible hours- ...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
$80.9k - $127.05k
...US-Nationwide-FIELD Full time 20186058 What Regulatory Affairs contributes to Cardinal Health Regulatory provides regulatory... ...Mansfield, MA. Job Summary The Principal Regulatory Affairs Specialist supports the Medical Solutions Regulatory Affairs team by...Full timeTemporary workWork experience placementLocal areaImmediate startRemote workFlexible hours- ...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
$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 SpecialistThis 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 audits...Work at office
$70k - $110k
...Shift Type Job Title Regulatory Affairs Specialist II Education Bachelor's Degree Location Minneapolis, MN 55401 US (Primary) Career Level Experienced (Non-Manager) Category Regulatory and Compliance Date Needed By Job Type Full-time...Full timeWork at officeShift work- ...The Science Team at Pride Health is hiring a "Regulatory Specialist" for a top materials science company. Key Responsibilities Manage U.S. product registrations and maintain regulatory documentation for assigned products. Support registration and re-registration activities...
- ...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
- ...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 market entry. You will prepare, review, and submit documentation, interface with agencies, and support release processes while maintaining...
- ...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
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
$80k - $120k
...pay range $80,000.00/yr - $120,000.00/yr Under general supervision, the individual in this role assists with medical writing and regulatory documentation, including preparation and finalization of test reports, regulatory filings, and review of marketing materials. Responsibilities...Full timeWork at office- ...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 Specialist, Ultrasound The Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and authorities to secure timely product clearances. Responsibilities include coordinating and preparing regulatory submission...Full timeWork at officeLocal areaWork 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...
$53k - $66k
...have a minimum of 2 years on-site compliance processing required, COS/TCCS/AHM certification preferred! Job Summary A Compliance Specialist will be responsible for auditing property files, assisting and training property staff in all areas regarding compliance with...Full timeWork at office$80k - $120k
...A medical equipment company is seeking a Mid-Senior level Quality Assurance professional to assist with regulatory documentation and medical writing. The role involves reviewing engineering test reports, monitoring regulatory requirements, and ensuring compliance with...Full timeWork at office- ...Boston Scientific is seeking a Senior Regulatory Affairs Specialist to support regulatory submissions and ongoing compliance for our active implantable device portfolio in a hybrid work model. The role requires strong US, EU, and international regulatory experience to...
- ...standard of care in neuromodulation to positively impact patient’s lives. Reporting to the Sr. Director, Regulatory Affairs, the Senior Regulatory Affairs Specialist will provide input to global regulatory strategies and support submission activities for Saluda Medical’...
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