Prin Regulatory Affairs Spec - Core Surgical innovations Medtronic PlcPrin Regulatory Affairs Spec - Core Surgical innovationsMounds View, MNResponsibilities include participating on product development teams, developing global regulatory strategies, preparing US and international regulatory submissions, supporting pre and post market regulatory compliance activities and evaluating proposed product changes for regulatory impact and preparing necessary documentation. If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Sr Regulatory Affairs Spec Medtronic PlcSr Regulatory Affairs SpecMounds View, MNThis role will partner closely with Geography Regulatory Affairs to support international submissions, government queries, registration documentation, product approval and clearance activities, product demand and release planning, and post-market regulatory compliance to help ensure continued product availability worldwide. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
Prin Regulatory Affairs Spec Medtronic PlcPrin Regulatory Affairs SpecMounds View, MNIf you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
Senior Regulatory Affairs Spec Medtronic PlcSenior Regulatory Affairs SpecMounds View, MNThe Senior Regulatory Affairs Specialist develops strategies for worldwide product registration with global regulatory agencies to introduce Diagnostic products, Programmers and Programming Software and accessories for Pacemakers and Defibrillators, Patient Monitors, and Software as a Medical Device to market, provides advice on regulatory requirements, prepares worldwide submissions and negotiates their approval. If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Senior Regulatory Affairs Spec MedtronicSenior Regulatory Affairs SpecMounds View, MinnesotaThe Senior Regulatory Affairs Specialist develops strategies for worldwide product registration with global regulatory agencies to introduce Diagnostic products, Programmers and Programming Software and accessories for Pacemakers and Defibrillators, Patient Monitors, and Software as a Medical Device to market, provides advice on regulatory requirements, prepares worldwide submissions and negotiates their approval. If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Director of Regulatory Affairs - RespirTech (Plymouth, MN) PhilipsDirector of Regulatory Affairs - RespirTech (Plymouth, MN)Plymouth, MN$171,000–$273,000 / yearYou're the right fit if: You've acquired 10+ years of experience working in Regulatory Affairs and/or Quality/Quality Operations within the FDA regulated Medical Device industry, including 3+ years of experience and a strong track record in successfully leading/managing Regulatory Affairs and/or Quality teams. Your role: Lead Regulatory Affairs strategy end-to-end execution (product inception through lifecycle management), driving innovation, actively providing value-added regulatory affairs input and deliverables for new 510k product introductions and product changes.
Director Of Regulatory Affairs - Respirtech (Plymouth, MN) PhilipsDirector Of Regulatory Affairs - Respirtech (Plymouth, MN)Plymouth, MN$171,000–$273,000 / yearYou're the right fit if: You've acquired 10+ years of experience working in Regulatory Affairs and/or Quality/Quality Operations within the FDA regulated Medical Device industry, including 3+ years of experience and a strong track record in successfully leading/managing Regulatory Affairs and/or Quality teams. Your role: Lead Regulatory Affairs strategy end-to-end execution (product inception through lifecycle management), driving innovation, actively providing value-added regulatory affairs input and deliverables for new 510k product introductions and product changes.
NewDirector Of Regulatory Affairs - Remote UnitedHealth Group Inc.Director Of Regulatory Affairs - RemoteEden Prairie, MNRemote$134,600–$230,800 / yearWorking closely with their team, legal and compliance colleagues, and business stakeholders, the Director of Regulatory Affairs will lead or support a wide range of regulatory activities, including regulatory assessments for new product/therapies and changes to existing products and the development and the execution of regulatory plans/strategies as required. The Director of Regulatory Affairs will be a member of the Legal Team responsible for providing the enterprise with strategic counsel and support on regulatory and quality matters related to medical devices, including software and algorithms, and other digital health technologies.
Manager, Regulatory & Payer Operations Support Coloplast CorpManager, Regulatory & Payer Operations SupportMinneapolis, MN$95,898–$143,847 / yearOur attention to detail, unmatched customer service, and dedication to helping our customers live happier, healthier lives are just a few of the many reasons we are one of the fastest growing catheter and ostomy supply companies in the nation! In coordination with other teams, will ensure proper staffing at all office locations and will ensure that offices are staffed during periods of PTO and staff development.
Manager, Regulatory & Payer Operations Support ColoplastManager, Regulatory & Payer Operations SupportMinneapolis, MN$95,898–$143,847 / yearOur attention to detail, unmatched customer service, and dedication to helping our customers live happier, healthier lives are just a few of the many reasons we are one of the fastest growing catheter and ostomy supply companies in the nation! In coordination with other teams, will ensure proper staffing at all office locations and will ensure that offices are staffed during periods of PTO and staff development.
Associate Director, Regulatory Affairs - Pulsed Field Ablation (PFA) Boston Scientific CorpAssociate Director, Regulatory Affairs - Pulsed Field Ablation (PFA)Arden Hills, MNThe Associate Director, Regulatory Affairs - Pulsed Field Ablation (PFA) is responsible for leading global regulatory strategy and execution for Boston Scientific's Pulsed Field Ablation portfolio, the company's most strategically critical and fastest-growing segment within Electrophysiology. In this role, you will provide strategic regulatory leadership and serve as the primary regulatory point of contact for PFA strategy, escalations, and program-level decision-making across new products, sustaining activities, global expansion, and compliance initiatives.
NewSenior Program Lead Regulatory Affairs 6010-Biosense Webster Legal EntitySenior Program Lead Regulatory AffairsPlymouth, MinnesotaAnalytical Reasoning, Business Writing, Coaching, Collaboration, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic Thinking . Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
NewSENIOR PROGRAM LEAD REGULATORY AFFAIRS Johnson & JohnsonSENIOR PROGRAM LEAD REGULATORY AFFAIRSPlymouth, MN$109,000–$174,800 / yearRequired Skills: Preferred Skills: Analytical Reasoning, Business Writing, Coaching, Collaboration, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic Thinking. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
NewSenior Program Lead Regulatory Affairs Johnson & JohnsonSenior Program Lead Regulatory AffairsPlymouth, MinnesotaAnalytical Reasoning, Business Writing, Coaching, Collaboration, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic Thinking . Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Senior Regulatory Affairs Manager Medtronic PlcSenior Regulatory Affairs ManagerMinneapolis, MNThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
NewSenior Regulatory Affairs Manager MedtronicSenior Regulatory Affairs ManagerMinneapolis, MinnesotaThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Regulatory Affairs Manager - International Compliance Operations – Structural Heart (on-site) AbbottRegulatory Affairs Manager - International Compliance Operations – Structural Heart (on-site)Saint Paul, MinnesotaOur portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. The candidate will leverage expertise in scientific, regulatory, and business considerations to ensure products developed, manufactured, or distributed comply with all applicable regulations.
Regulatory Affairs, Sr Manager - Obesity And Related Conditions Amgen Inc.Regulatory Affairs, Sr Manager - Obesity And Related ConditionsWashington, MNIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.
Senior Environmental Regulatory Permitting Manager - FERC Stantec IncSenior Environmental Regulatory Permitting Manager - FERCMinneapolis, MNProvide technical leadership and project management for oil & gas midstream permitting projects (FERC-regulated natural gas or liquids pipeline projects) and energy transition projects throughout the US. Primary Location: United States | IL | Chicago Organization: 1937 EnvSvcs-US Great Lakes East-Chicago IL Employee Status: Regular Business Justification: New Position Travel: No Schedule: Full time Job Posting: 21/04/2026 02:04:51 Req ID: 1005490.
Staff Global Regulatory GPO DanaherStaff Global Regulatory GPOChaska, MinnesotaRemoteBachelor’s degree in applicable fields (such as biological sciences, biomedical engineering, or chemistry) with 9+ years of related work experience OR Master's degree in applicable field with 7+ years of related work experience OR Doctoral degree in applicable field with 4+ years of related work experience. The Staff Global Regulatory Affairs ensures that Beckman Coulter products, processes, and documentation adhere to global premarket regulations for registration lifecycle management, global labeling requirements and marketing material review and approval procedures.
Regulatory Compliance Analyst - Pharmacy Licensing Rose InternationalRegulatory Compliance Analyst - Pharmacy LicensingEden Prairie, Minnesota$27.50 / hourTemporary
Regulatory Affairs Manager - International Compliance Operations - Structural Heart (on-site) Abbott LaboratoriesRegulatory Affairs Manager - International Compliance Operations - Structural Heart (on-site)New Brighton, MN$99,300–$198,700 / yearOur portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. The candidate will leverage expertise in scientific, regulatory, and business considerations to ensure products developed, manufactured, or distributed comply with all applicable regulations.
Commercial & Healthcare Regulatory Counsel Alto IncCommercial & Healthcare Regulatory CounselMNRemote$135,000–$185,000 / yearPhysical requirements for this role include the ability to work at a computer terminal with monitor, keyboard and mouse for extended periods of time, stoop, bend, and reach for equipment and supplies, make frequent repetitive motions required to operate a computer that include the wrists, hands and fingers, and lift, carry, push, pull, and move light objects up to 20 pounds. Issue-spot and provide practical guidance on applicable laws and regulations, such as the Anti-Kickback Statute (AKS), Stark Law, False Claims Act, FDA/DEA requirements relevant to pharmacy and telehealth operations, state pharmacy/professional licensing, PBM contracting/network participation, and HIPAA/HITECH.
Sr. Manager, Food Safety, Quality & Regulatory (FSQR) JonnyPopsSr. Manager, Food Safety, Quality & Regulatory (FSQR)Plymouth, MNFull timeOversee the interpretation and communication of environmental and finished product testing data, guiding teams in identifying risk trends, prioritizing corrective actions, and implementing proactive interventions to safeguard product quality and food safety. This role partners closely with plant QA teams, R&D, Supply Chain, Procurement, and external stakeholders to ensure that systemic risks are identified, trends are understood, and resources are focused where they will have the greatest impact on food safety and product quality.
Entry Level Chemical Regulatory Analyst Pace Analytical ServicesEntry Level Chemical Regulatory AnalystMinneapolis, MinnesotaThis position is part of a global team that provides a full spectrum of chemical substance regulatory support to business groups and functional areas from all divisions in the company including technical, R&D, marketing, product stewardship, and sales teams. Candidate will analyze customer products to maintain regulatory compliance, and complete data gaps for compliance in this intermediate to upper-intermediate scientific, non-laboratory position.
Director, Regulatory Operations Keros TherapeuticsDirector, Regulatory OperationsLexington, MN$206,000–$227,000 / yearWith a focus on developing differentiated product candidates that are designed to alter TGF- signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. Primary Responsibilities: Oversee all Regulatory Operations deliverables, including management of Health Authority correspondence/submission archives, business administration of the Veeva Vault Regulatory Information Management system, submission management, and training of associated business processes.
Senior Consultant - MedTech Regulatory Implementation Veeva Systems IncSenior Consultant - MedTech Regulatory ImplementationMinneapolis, MNRemote$80,000–$200,000 / yearThe MedTech Regulatory consultant will work closely with Professional Services teams to ensure delivery success across the end-to-end regulatory process, covering both data and documentation related workstreams. Veeva is looking for an experienced consultant to lead MedTech Regulatory Information Management (RIM) implementations at Veeva's MedTech customers globally.
Regulatory Solutions Advisor 3ERegulatory Solutions AdvisorWashington, MNPartnering closely with Sales, you'll deliver impactful, scalable solutions, including 3E's growing AI-powered capabilities, that help clients achieve their business goals while advancing a safer, more sustainable world. Impactful Work: Help customers solve complex regulatory challenges while contributing to safer products, workplaces, and supply chains across the globe.
Director, Quality & Regulatory- Mergers & Acquisitions (M&A) PhilipsDirector, Quality & Regulatory- Mergers & Acquisitions (M&A)Plymouth, MN$181,000–$288,000 / yearEnsure successful transition and exit of transition services, including full transfer of Q&R responsibilities and retirement of TSLA obligations prior to completion of Day 2. You're the right fit if: You have a minimum of 15+ years' experience in FDA regulated global medical device environments (Class III products/devices preferred) with demonstrated experience/expertise in cross-functional Program leadership/management, focused on Quality/regulatory compliance, change management and M&A within global/matrixed medical device organizations. The Director, Quality & Regulatory M&A is an enterprise Q&R leader for M&A activities and primary interface to deal teams, providing end-to-end leadership across the transaction lifecycle, with a focus on complex divestitures, carve-outs, and separations.
Hardgoods Regulatory Engineering Risk and Compliance Supervisor 3M CoHardgoods Regulatory Engineering Risk and Compliance SupervisorMaplewood, MN$145,676–$178,049 / yearStrong project management skills and proven ability to work independently, manage multiple global projects, have a thirst for learning, and drive for tangible results in a fast-paced, cross-functional environment. Five (5) years combined experience in Product Compliance, Product Stewardship, Sustainability, Materials science, Quality, or related Regulatory Affairs role in a private, public, government or military environment.
Hardgoods Regulatory Engineering Risk And Compliance Supervisor 3M CompaniesHardgoods Regulatory Engineering Risk And Compliance SupervisorMaplewood, MN$145,676–$178,049 / yearStrong project management skills and proven ability to work independently, manage multiple global projects, have a thirst for learning, and drive for tangible results in a fast-paced, cross-functional environment. Five (5) years combined experience in Product Compliance, Product Stewardship, Sustainability, Materials science, Quality, or related Regulatory Affairs role in a private, public, government or military environment.
Sr Prin Clinical Research Specialist- Post Market Surveillance and Evidence MedtronicSr Prin Clinical Research Specialist- Post Market Surveillance and EvidenceMounds View, MinnesotaThe role functions in a strategic advisory capacity, helping teams understand how to identify and leverage different RWD sets for regulatory purposes, evaluate potential RWE approaches, assess available data sources, and identify opportunities where real world evidence may complement traditional clinical evidence. Partners with PACS therapy teams, Regulatory Affairs leadership, HEOR leadership, and operating unit clinical teams to evaluate opportunities where real world data and real-world evidence may address regulatory questions or complement traditional clinical trial evidence.
Labeling Specialist Actalent IncLabeling SpecialistMaple Grove, MN$40–$60 / hourThe Labeling Specialist ensures all labels meet regulatory, quality, and packaging requirements throughout the label lifecycle, while collaborating with cross-functional teams in a fast-paced, growth-oriented medical device organization. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
Clinical Affairs Specialist, Interventional Coronary (REMOTE) Teleflex IncClinical Affairs Specialist, Interventional Coronary (REMOTE)Minneapolis, MN$92,800–$139,200 / yearOur portfolio includes a broad range of clinically relevant products, such as the GuideLiner and Turnpike Catheters; the Orsiro Mission Drug-Eluting Stent; the PK Papyrus Covered Coronary Stent; the Ringer Perfusion Balloon Catheter; the Pulsar -18 T3 Self-Expanding Stent; Passeo Balloon Catheters; and the OnControl Powered Bone Access System. Collaborate cross-functionally with Marketing, Sales, Engineering, and other internal teams on strategic initiatives and product-related activities, applying critical thinking and clinical judgment to evaluate information, address challenges, and support informed decision-making within established.
NewClinical Affairs Specialist, Interventional Oncology (REMOTE) Teleflex IncClinical Affairs Specialist, Interventional Oncology (REMOTE)Minneapolis, MN$110,000–$120,000 / yearOur portfolio includes a broad range of clinically relevant products, such as the GuideLiner and Turnpike Catheters; the Orsiro Mission Drug-Eluting Stent; the PK Papyrus Covered Coronary Stent; the Ringer Perfusion Balloon Catheter; the Pulsar -18 T3 Self-Expanding Stent; Passeo Balloon Catheters; and the OnControl Powered Bone Access System. Collaborate cross-functionally with Marketing, Sales, Engineering, and other internal teams on strategic initiatives and product-related activities, applying critical thinking and clinical judgment to evaluate information, address challenges, and support informed decision-making within established company policies and practices.
Labeling Specialist Teleflex IncLabeling SpecialistMaple Grove, MN$69,700–$89,600 / yearThe pay range for this position at commencement of employment is expected to be between ($69,700-$89,600) however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Additionally, they will apply advanced project management expertise, deliver labeling process training, and collaborate across internal functions and external agencies to ensure regulatory compliance to support business objectives.
NewLabeling Specification Specialist Actalent IncLabeling Specification SpecialistMounds View, MN$30–$38 / hourAs a Labeling Specification Specialist, you"ll play a critical role in creating and managing product labeling, packaging artwork, and specifications that support global product launches and ongoing product lifecycle management. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Sr Prin Clinical Research Specialist- Post Market Surveillance and Evidence Medtronic PlcSr Prin Clinical Research Specialist- Post Market Surveillance and EvidenceMounds View, MNThe role functions in a strategic advisory capacity, helping teams understand how to identify and leverage different RWD sets for regulatory purposes, evaluate potential RWE approaches, assess available data sources, and identify opportunities where real world evidence may complement traditional clinical evidence. Partners with PACS therapy teams, Regulatory Affairs leadership, HEOR leadership, and operating unit clinical teams to evaluate opportunities where real world data and real-world evidence may address regulatory questions or complement traditional clinical trial evidence.
Senior HR Service Delivery Specialist - HR Compliance Specialist Wolters Kluwer N.V.Senior HR Service Delivery Specialist - HR Compliance SpecialistMinneapolis, MN$71,300–$124,500 / yearWhile the position does not have direct people management responsibilities, it requires strong project leadership, influence, stakeholder management, and accountability for delivering compliance-focused outcomes across the enterprise. This role helps mitigate organizational risk, strengthens operational controls, and promotes consistent application of employment-related policies and practices across a multi-state organization.
NewQuality Systems Specialist Actus NutritionQuality Systems SpecialistEden Prairie, MNTrack quality documents requests in HubSpot, report monthly metrics, and work with corporate quality managers to complete requests and responses on time. Essential Responsibilities: Support Food Safety, Quality Assurance, and Regulatory Affairs teams by coordinating meetings, and managing corporate Quality Assurance SOPs.
NewQuality Systems Specialist Milk SpecialtiesQuality Systems SpecialistEden Prairie, MNTrack quality documents requests in HubSpot, report monthly metrics, and work with corporate quality managers to complete requests and responses on time. Essential Responsibilities: Support Food Safety, Quality Assurance, and Regulatory Affairs teams by coordinating meetings, and managing corporate Quality Assurance SOPs.
Senior Sales Specialist - Infectious Disease Diagnostics - Urgent Care - Abbott LaboratoriesSenior Sales Specialist - Infectious Disease Diagnostics - Urgent Care -Minneapolis, MN$78,000–$156,000 / yearThe Senior Specialist - Urgent Care will be responsible to analyze, profile, and develop strategic relationships with targeted urgent care accounts while partnering with distribution channel partners and internal Abbott divisions to prioritize and qualify customers in order to penetrate and close new business opportunities to achieve the financial goals for the business. Build and maintain strong relationships with executive-level customers, key opinion leaders, distributors, and industry partners to drive customer retention, competitive conversions, and advocacy for Abbott products and solutions.
Sr. Principal Clinical Research Specialist Integrated Resources, IncSr. Principal Clinical Research SpecialistMounds View, MNSummary: Our CER-OMA team supports our clinical-regulatory filings for all pre-market and post-market technologies across all geographies and support our global medical affairs operations with real-time scientific use-case assessments and dissemination. Required Knowledge and Experience: Requires mastery level knowledge of specialty area and working knowledge of several other areas, typically obtained through advanced education combined with experience.
Clinical Strategy Specialist Artech LLCClinical Strategy SpecialistMaple Plain, TNThe Global Clinical Strategy Lead for Orthopedics and Robotics is responsible for developing and executing global clinical and economic evidence generation strategies to support new product introduction, expand adoption, and ensure continued regulatory approval and market access. This role works across the full product lifecycle, partnering closely with cross-functional teams including R&D, clinical operations, regulatory affairs, HEOR, medical affairs, and marketing to align evidence strategies with business and regulatory needs.
NewQuality Systems Specialist Milk Specialties CompanyQuality Systems SpecialistEden Prairie, MN$70,000–$80,000 / yearPart timeTrack quality documents requests in HubSpot, report monthly metrics, and work with corporate quality managers to complete requests and responses on time. The Quality Systems Specialist supports administrative tasks, document maintenance, communication, regulatory program, and quality assurance audit support.
Sr. Sales Specialist, Govt. HighQ & Partnership Sales Thomson ReutersSr. Sales Specialist, Govt. HighQ & Partnership SalesEagan, District of ColumbiaRemoteFinally, Thomson Reuters offers the following additional benefits: optional hospital, accident and sickness insurance paid 100% by the employee; optional life and AD&D insurance paid 100% by the employee; Flexible Spending and Health Savings Accounts; fitness reimbursement; access to Employee Assistance Program; Group Legal Identity Theft Protection benefit paid 100% by employee; access to 529 Plan; commuter benefits; Adoption & Surrogacy Assistance; Tuition Reimbursement; and access to Employee Stock Purchase Plan. Serve as the subject matter expert and primary sales driver for HighQ within the Government segment, articulating its value as a platform that eliminates barriers to service delivery, minimizes administrative burden, and reduces overhead costs by streamlining document sharing, task allocation, and data transparency — while seamlessly integrating to lessen the risk of missing vital information.
NewQuality Systems Specialist Actalent IncQuality Systems SpecialistLakeville, MN$25–$31.73 / hourThis role provides operational and systems support across certifications, regulatory registrations, digital platforms, and KPI tracking, ensuring that documentation and resources are accurate, up-to-date, and easily accessible to relevant stakeholders. The role reports into the Quality Management Systems function and partners closely with the QMS team, including another team member in a similar function, while supporting broader Quality & Food Safety initiatives across the organization.
AML/BSA Specialist eTeam Inc.AML/BSA SpecialistMinneapolis, MN$28–$31.07 / hourThis role supports Financial Crimes Controls by analyzing reporting data, managing review and remediation cases, coordinating with internal partners to resolve data defects, and maintaining required documentation and evidence to demonstrate control execution. The Payments Financial Crimes Operations Analyst is responsible for researching, remediating, actioning, and reporting on customer and account records routed to an in process compliance queue.
Cleaning Validation Specialist Karwell TechnologiesCleaning Validation SpecialistSt. Paul, MNOur client, a leading biologics manufacturing company, is seeking an experienced Cleaning Validation Specialist to support cleaning validation activities for equipment upgrade projects within a cGMP manufacturing environment. The ideal candidate will have hands-on pharmaceutical or biotechnology cleaning validation experience, strong technical writing skills, and the ability to work collaboratively with cross-functional teams.
Tissue Specialist I eTeam Inc.Tissue Specialist IPlymouth, MNThis role requires exceptional attention to detail, strong fine motor skills, and the ability to perform intricate sewing tasks using suture and needle under a microscope. " Utilize small hand tools, calibrated instruments, measuring equipment, microscopes, and test fixtures.