Regulatory Affairs Specialist
Russell Tobin
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. You will maintain electronic records, support UDI activities, and assist with compliance tasks. Notary duties may be required; 12-month assignment with competitive hourly pay on W2. #J-18808-Ljbffr
- Regulatory Affairs Specialist III - Maplewood, MN (Hybrid) Contract Duration: 18 months (possible extension). Pay Rate Range: $45.00/hr - $55.00/hr on W2. Work Authorization: Only U.S. Citizen or Green Card holder. About VARITE VARITE is an American‑headquartered life...SuggestedContract work
- 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...Suggested
- 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...Suggested
- ...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...Suggested
- ...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...Suggested
- Medtronic plc busca un Especialista en Asuntos Regulatorios para desarrollar estrategias de registro mundial y apoyar la presentación de expedientes ante agencias regulatorias como FDA y EU MDR. Se requiere experiencia en dispositivos médicos, conocimientos de normativas...
$74.4k - $111.6k
...engineer the extraordinary. In collaboration with leading clinicians, researchers, and scientists worldwide, Role Overview The Regulatory Affairs Specialist develops strategies for worldwide product registration with Medtronic Geography Regulatory partners and global...H1bWork at officeLocal areaWorldwideFlexible hours- ...Job Title: Regulatory Affairs Specialist III Location: Maplewood, MN Duration: 18 Months+ Pay: $50/hr. on W2 Description : When you're part of ***, you'll do challenging work while collaborating with a team that values performance, quality, innovation,...Monday to FridayFlexible hours
$120k - $180k
...support worldwide. This individual will also perform other regulatory duties.As one of three comprehensive portfolios at Medtronic... ...there.We are looking for a passionate Principal Regulatory Affairs Specialist with experience developing global regulatory strategies and...Full timeH1bWork at officeLocal areaImmediate startWorldwideRelocationFlexible hours$120k - $180k
...performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary. The Principal Regulatory Affairs Specialist will play a key role in launching new products and sustaining the Pain Interventions product portfolio. As a core member...Full timeH1bWork at officeLocal areaImmediate startWorldwideFlexible hours$50 per hour
...Regulatory Affairs Specialist III Our client, a leading organization in the life sciences and healthcare industry, is seeking a Regulatory Affairs Specialist III to join their team. As a Regulatory Affairs Specialist III, you will be part of the Regulatory Affairs &...Weekly payTemporary workFlexible hours$60k - $120k
...Regulatory Operations Specialist I Abbott 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...For contractorsWork experience placementWorldwideShift work$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...H1bWork at officeLocal areaImmediate startFlexible hours$74.4k - $111.6k
...Regulatory Affairs Specialist Medtronic's Access and Instruments Operating Unit develops technologies that support surgical access and enable precise, efficient procedures across a range of care settings. The portfolio includes products and solutions designed to help...Local areaFlexible hours- 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
- Our client, a leader in the healthcare industry, is seeking a Regulatory Affairs Specialist to join their team. As a Regulatory Affairs Specialist, you will be part of the Regulatory Affairs Department supporting global post-market compliance activities. The ideal candidate...Weekly payTemporary workFlexible hours
- The Regulatory Affairs Specialist will play a key role in supporting regulatory strategy and compliance throughout the product lifecycle. Reporting to the Global Product Director, this individual will partner closely with Engineering, Quality, Operations, Manufacturing,...InternshipWork at office
$85k - $104k
...policies. ESSENTIAL FUNCTIONS OF THE POSITION: Support global regulatory pre-market applications for geographies included but not... ...applicable regulations (Change Control) Work with Regulatory Affairs staff, engineers and technical experts to resolve potential regulatory...Contract workTemporary workFor contractorsFor subcontractorWork at officeLocal areaRemote workWorldwide- ...Senior Regulatory Affairs Specialist Location: Saint Paul, MN 55112 Duration: 6 Months Work Arrangement: 100% Onsite Position Overview Submission Readiness & Execution. Provide Regulatory Affairs support for multiple global submissions by coordinating submission readiness...Temporary workWork at officeFlexible hours
- ...Medtronic Regulatory Affairs Specialists lead worldwide product registrations with Geography Regulatory partners and global agencies. They provide expert advice, prepare submissions, support approvals, and assist with license maintenance, including annual reports and...Worldwide
$113.03k - $165.77k
...right Responsibilities Adheres to Integer's Core Beliefs and all safety and quality requirements. Develops US and International regulatory strategies for product submissions, identifying needs for bench, animal and clinical testing. Provides strategic input. Participates...Immediate start- ...Abbott's Electrophysiology business in Plymouth, Minnesota, seeks a regulatory affairs specialist to prepare documentation for regulatory submissions in heart disease treatment. The role involves collaborating with teams, ensuring compliance with FDA standards, and supporting...
- ...Medtronic is seeking a Senior Regulatory Affairs Specialist to lead worldwide product registration strategies and regulatory submissions for Medtronic Pelvic Health. The role partners with geography teams, engineers, and regulatory staff to ensure timely approvals and...Worldwide
- ...Attorney Search in Minneapolis seeks an associate or senior attorney with 5–10 years of energy transactional experience to join the Regulatory Affairs group. The role focuses on Power Purchase Agreements, Interconnection Agreements, Large Load matters, electric service...
- ...A leading contract research organization is looking for a Senior Regulatory Affairs Manager in Minneapolis, MN. The role involves managing regulatory submissions, ensuring compliance with FDA regulations, and providing guidance during product development. Candidates should...Contract work
$131k - $143k
...collaborative, purpose-driven environment where experienced regulatory professionals can influence global product strategy, partner... ...technologies to market. About the Role The Principal Regulatory Affairs Specialist develops and executes regulatory strategies for medical...- IT Compliance Analyst Location: Little Canada MN Contract: 12+ months contract to hire Pay range: $36 - $38/hr on W2 Our Fortune 500 client (One of the world's largest Medical Device companies) is looking for hardworking, motivated talent to join their innovative team....Contract work
$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$22 - $25 per hour
...Credentialing Specialist Hot Job Hybrid • Midwest Physicians Services - MPS - Roseville, MN 55113 Overview Salary Range $22.00 - $25.00 Hourly Position Type Full Time Job Shift Day Education Level High School Category Business Office, Administration, Credentialing...Hourly payFull timeWork at officeRemote workMonday to FridayShift work$94k - $150k
...Senior Regulatory Affairs Specialist 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 documents for...Full timeWork at officeImmediate startWork visaRelocation package3 days per week
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