NewSenior Cyber Specialist – Digital Enablement Epitec, IncSenior Cyber Specialist – Digital EnablementLittle Canada, MNYou will partner closely with internal product owners, developers, engineers, security architects, and external collaborators to evaluate solutions, strengthen governance, and guide secure product development. You will evaluate the cybersecurity posture of new and existing product technologies, identify risks, recommend mitigation strategies, and ensure timely remediation and closure.
NewCybersecurity Specialist - Cyber Data Services Epitec, IncCybersecurity Specialist - Cyber Data ServicesLittle Canada, MN$50–$55 / hourIn this role, you will act as a trusted advisor to internal product, information technology, engineering, and security stakeholders, helping them successfully onboard, access, and operationalize cyber data for security analytics, detection, compliance, operational monitoring, and product security use cases. This role focuses on cyber data readiness, adoption, and use, and partners closely with detection engineering, event detection, and incident response teams by enabling high-quality, accessible, and well-governed data.
Principal Regulatory Affairs Specialist Elucent Medical IncPrincipal Regulatory Affairs SpecialistEden Prairie, MN$120,000–$135,000 / yearThe Principal Regulatory Affairs Specialist independently performs regulatory impact assessments for product design, manufacturing, labeling, software, process, supplier, and site changes; prepares technical documentation and regulatory submissions; supports implementation of regulatory pathways and strategies established by the Regulatory Affairs Director; and provides regulatory analysis to support product development, commercialization, change control, and post-market activities. Required: direct, hands-on experience preparing and supporting FDA 510(k)s for medical devices, including substantial equivalence documentation, submission compilation, FDA question responses, and clearance support.
NewPrincipal Regulatory Affairs Specialist Elucent MedicalPrincipal Regulatory Affairs SpecialistEden Prairie, MinnesotaThe Principal Regulatory Affairs Specialist independently performs regulatory impact assessments for product design, manufacturing, labeling, software, process, supplier, and site changes; prepares technical documentation and regulatory submissions; supports implementation of regulatory pathways and strategies established by the Regulatory Affairs Director; and provides regulatory analysis to support product development, commercialization, change control, and post-market activities. Required: direct, hands-on experience preparing and supporting FDA 510(k)s for medical devices, including substantial equivalence documentation, submission compilation, FDA question responses, and clearance support.
Advanced Regulatory Affairs Specialist Bio-TechneAdvanced Regulatory Affairs SpecialistMinneapolis, MinnesotaBy joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. This role operates with limited supervision and is responsible for ensuring compliant and efficient execution of regulatory deliverables across the product lifecycle.
International Regulatory Affairs Specialist Mclaughlin Gormley KingInternational Regulatory Affairs SpecialistBrooklyn Park, Minnesota$90,000–$100,000 / yearMGK has 100+ years' of experience focusing on sustainable & environmentally conscious ways to protect families and crops from pests around the world, using our synthetic and certified organic, botanically based pesticide products. This role requires close collaboration with sales and marketing to support compliant product strategies and effectively prioritize and manage related projects.
Principal Regulatory Affairs Specialist Medtronic PlcPrincipal Regulatory Affairs SpecialistMounds View, MNThis role is responsible for shaping and executing global regulatory strategies, with a strong focus on pre-market submissions and early engagement with the global regulatory partners and/or regulatory authorities, as appropriate, across the United States, European Union, China, Japan, and Australia. Strategic direction is expected to support a number of regulatory applications which may include, FDA Pre-submissions, PMDA consultations, original IDEs and PMAs, IDE and PMA Supplements/Reports, Shonin applications, China PTR submissions, and EU MDR Technical Documentation.
Regulatory Affairs Specialist Heraeus Holding GmbHRegulatory Affairs SpecialistFridley, MN$110,178–$120,000 / yearWhat We're Looking For: Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Pharmacy, Biology, or Chemistry and 5 years of experience as a Medical Device Regulatory Affairs Specialist, Medical Device Quality Engineer, or Medical Device Design Engineer. Alternatively, Master's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Pharmacy, Biology, or Chemistry 2 years of experience as a Medical Device Regulatory Affairs Specialist, Medical Device Quality Engineer, or Medical Device Design Engineer.
Regulatory Affairs Specialist II Stereotaxis IncRegulatory Affairs Specialist IIMinneapolis, MNPosition Summary: The Regulatory Affairs Specialist II provides hands-on regulatory affairs support for new product marketing approvals and renewals for existing products, including development of regulatory requirements/strategies and preparation of submissions. These innovations help physicians provide unsurpassed patient care with robotic precision and safety, improved lab efficiency and productivity, and enhanced integration of procedural information.
Regulatory Affairs Specialist Oxenham Group LLCRegulatory Affairs SpecialistEagan, MNThe Regulatory Affairs Specialist will maintain global registrations and technical documentation, support audits, manage product compliance throughout the lifecycle, and provide strategic regulatory input to cross-functional teams. Maintain and update European technical files, including risk assessments, usability reports, and clinical evaluations.
Regulatory Affairs Specialist Stryker CorpRegulatory Affairs SpecialistBloomington, MN$76,100–$126,900 / yearHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. Support change control activities within PLM systems, including coordinating documentation updates, routing change orders, and ensuring appropriate reviewers and approvers are assigned.
Senior Regulatory Affairs Specialist PhilipsSenior Regulatory Affairs SpecialistMN$99,000–$157,000 / yearThe actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity. • Lead global regulatory intelligence initiatives, contribute to regulatory and product registration strategies, and help implement global regulatory roadmaps based on the competitive landscape and marketing objectives.
NewRegulatory Affairs Specialist Medtronic PlcRegulatory Affairs SpecialistPlymouth, 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).
Principal Regulatory Affairs Specialist - Advertising & Promotion Boston Scientific CorpPrincipal Regulatory Affairs Specialist - Advertising & PromotionArden Hills, MNThe anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. As a key regulatory partner to the commercial organization, this role helps enable compliant and effective communications that support business objectives while protecting patients and the company.
Principal Regulatory Affairs Specialist - Advertising & Promotion (Ad Promo) Boston Scientific CorpPrincipal Regulatory Affairs Specialist - Advertising & Promotion (Ad Promo)Maple Grove, MNThe anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Your responsibilities will include: Review and provide regulatory feedback on advertising and promotional materials, including print, digital, web, email, social media, video, webinars, sales aids and training materials.
NewRegulatory Affairs Specialist -Neuro MedtronicRegulatory Affairs Specialist -NeuroMinneapolis, MinnesotaIf 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).
Regulatory Specialist 1 or 2 (Research Professional 1 or 2) University of MinnesotaRegulatory Specialist 1 or 2 (Research Professional 1 or 2)Minneapolis, MN$57,000–$61,000 / yearp>At the University of Minnesota, we are proud to be recognized by the Star Tribune as a Top Workplace for 2021, as well as by Forbes as Best Employers for Women and one of America's Best Employers (2015, 2018, 2019, 2023), Best Employer for Diversity (2019, 2020), Best Employer for New Grads (2018, 2019), and Best Employer by State (2019, 2022). Located at the heart of one of the nations most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.
Regulatory Affairs Specialist II - Electrophysiology (on-site) Abbott LaboratoriesRegulatory Affairs Specialist II - Electrophysiology (on-site)Plymouth, MN$61,300–$122,700 / 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. In Abbott's Electrophysiology (EP) business, we're advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.
Regulatory Affairs Specialist Patterson Companies IncRegulatory Affairs SpecialistSt Paul, MN$77,200–$100,333.33 / yearStrong verbal and written communications with ability to effectively communicate at specialist and line management levels in the organization; strong customer service-oriented skills. Ability to work effectively within a team and as an individual contributor in a fast-paced changing environment -- multi-tasks, prioritizes and meet deadlines in timely manner.
Principal Regulatory Affairs Specialist Boston Scientific CorpPrincipal Regulatory Affairs SpecialistMaple Grove, MNThe anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) see www.bscbenefitsconnect.comwill vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Represent the Regulatory Affairs function on cross-functional teams for new product development and sustaining activities, including manufacturing changes, site transfers and continuous improvement projects.
Advanced Regulatory Affairs Specialist Bio-Techne CorpAdvanced Regulatory Affairs SpecialistMinneapolis, MN$49,700–$81,650 / yearWhy Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics.
NewRegulatory Affairs Specialist Teleflex IncRegulatory Affairs SpecialistMaple Grove, MN$88,000–$130,000 / yearMust possess a basic understanding of product risk/benefit concepts, working knowledge of US and International regulations applicable to market authorization for Vascular products, good verbal communication, technical writing, intra- and interdepartmental communication, and collaboration skills. The pay range for this position at commencement of employment is expected to be between $88,000.00 - $130,000.00; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.
Regulatory Affairs Intelligence Specialist AbbottRegulatory Affairs Intelligence SpecialistSaint Paul, MinnesotaBachelors Degree (± 2 years) In science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields is preferred OR an equivalent combination of education and work experience . This position serves as the Medical Devices Regulatory Affairs (RA) Global Regulatory Compliance process lead; collaborates cross-functionally as needed and keeps MD RA informed of key global regulatory changes and status of assessment / implementation for compliance via the QMS Process.
Regulatory Affairs Specialist -Neuro Medtronic PlcRegulatory Affairs Specialist -NeuroMinneapolis, MNThis role involves: \n\n Providing expert advice on regulatory requirements \n \n\n Preparing submissions \n \n\n Supporting approval activities \n \n\n Assisting with license maintenance, including annual reports, renewals, design/manufacturing change notifications, QMS audits, and manufacturing site registrations \n \n\n \nA Day In The Life \n\n Team with business unit Regulatory Affairs Specialists (RAS) and international regulatory staff to provide regulatory support for new products/therapies and changes to existing products. Please note some of the above benefits may not apply to workers in Puerto Rico.\n \nFurther details are available at the link below:\n \nMedtronic benefits and compensation plans\n \nAbout Medtronic\n \nWe lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.\n \nOur Mission \u2014 to alleviate pain, restore health, and extend life \u2014 unites a global team of 95,000+ passionate people.
Senior Regulatory Affairs Specialist - Onsite Medtronic PlcSenior Regulatory Affairs Specialist - OnsiteMinneapolis, 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.
Senior Regulatory Affairs Specialist - Onsite MedtronicSenior Regulatory Affairs Specialist - OnsiteMinneapolis, MinnesotaIf 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 herea 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).
Product Regulatory Specialist Actalent IncProduct Regulatory SpecialistNew Hope, MN$38–$41 / hourThe environment provides exposure to a wide variety of products, regulations, and cross-functional partners, and is well-suited for someone who enjoys problem-solving, structured processes, and working across teams in a professional office setting. 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.
NewPrincipal Regulatory Affairs Specialist: Pelvic Health MedtronicPrincipal Regulatory Affairs Specialist: Pelvic HealthMinneapolis, MinnesotaPrefer a candidate located in the Minneapolis area or who can relocate there. We are looking for a passionate Principal Regulatory Affairs Specialist with experience developing global regulatory strategies and leading worldwide Clinical Trial Applications (CTAs) for our innovative, high-risk medical device portfolio. Designed to modulate nerve pathways and restore communication between the brain and pelvic floor, these programmable therapies deliver personalized treatment supported by strong clinical evidence and long-term outcomes—helping improve confidence, independence, and quality of life.
Product Regulatory Specialist (Hybrid) Actalent IncProduct Regulatory Specialist (Hybrid)New Hope, MN$38.46–$41.35 / hourWe 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. Collaborate closely with product development, supply chain, project management, marketing, and sales teams to ensure the global compliance of marketed lubricants.
Product Regulatory Specialist- Hybrid Actalent IncProduct Regulatory Specialist- HybridNew Hope, MN$38.46–$41.35 / hourWe 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. Collaborate closely with product development, supply chain, project management, marketing, and sales teams to ensure the global compliance of marketed lubricants.
NewRegulatory Specialist Pride GlobalRegulatory SpecialistMaplewood, MN$25–$27 / hourOnly 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. This role involves working with regulatory affairs personnel across 80+ countries who are responsible for registering or re-registering medical devices and pharmaceutical products locally.
Regulatory Affairs Specialist - Electrophysiology (on-site) Abbott LaboratoriesRegulatory Affairs Specialist - Electrophysiology (on-site)Plymouth, MN$50,700–$101,300 / yearSupports all business segment initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for regulatory registration, ensuring products and procedures comply with regulatory agency specifications.
NewRegulatory Specialist Pride Technologies LLCRegulatory SpecialistMaplewood, MN$25–$27 / hourOnly 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. Job Description: This role involves working with regulatory affairs personnel across 80+ countries who are responsible for registering or re-registering medical devices and pharmaceutical products locally.
Regulatory & Clinical Specialist LivaNova PlcRegulatory & Clinical SpecialistMinneapolis, MNRemote$85,000–$95,000 / yearManage the overall development and approval process for assigned documents (CEP, CER, etc.) within timelines, including documentation generation, initiation of the review process, discussions on proposed revisions, and document completion in collaboration with other team members. The Regulatory and Clinical Specialist is a liaison with the organization working with various groups to effectively communicate and collaborate on the deliverables and meet the project deadlines in line with the regulatory requirements.
Healthcare Regulatory Specialist- PACE Volunteers of America, Inc.Healthcare Regulatory Specialist- PACEEden Prairie, MNRemote$90,000–$100,000 / yearFull timeExperience: Requires a minimum of three (3) years of progressively responsible experience in healthcare compliance, regulatory oversight, auditing, or survey management, including direct responsibility for interpreting regulations, supporting audits or surveys, reviewing policies for regulatory alignment, and advising operational or clinical leaders on compliance requirements, preferably in senior care settings such as skilled nursing, assisted living, or PACE. •PACE Specialist: Serve as regulatory resource for participant rights, IDT processes, service authorization timeliness, homecare supervisory expectations, contracted provider compliance, grievances/ appeals, and adherence to the PACE three-way agreement.
Regulatory Affairs Intelligence Specialist Abbott LaboratoriesRegulatory Affairs Intelligence SpecialistMN$61,300–$122,700 / yearBachelors Degree (± 2 years) In science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields is preferred OR an equivalent combination of education and work experience. This position serves as the Medical Devices Regulatory Affairs (RA) Global Regulatory Compliance process lead; collaborates cross-functionally as needed and keeps MD RA informed of key global regulatory changes and status of assessment / implementation for compliance via the QMS Process.
NewRegulatory Documentation Specialist Volt Information Sciences IncRegulatory Documentation SpecialistMaplewood, MNWhy This Role is Exciting Work with teams from 80 countries - truly global exposure Build a strong career in Regulatory Affairs high-demand domain Gain hands-on experience in international compliance & documentation Get certified as a Notary company-supported Work in a collaborative learning-driven environmentWere Looking For Bachelors degree in Science or Engineering Strong attention to detail and organizational skills Good communication skills for global coordination Proficiency in Microsoft Office Excel Word Outlook Eagerness to learn and grow in a global corporate environmentPay Range 27 to 30.30 per hour. Come create your career with VoltRole Regulatory Documentation SpecialistLocation Maplewood MNExpected Duration 6 monthsKickstart or grow your career in global regulatory affairs Join a fast-paced collaborative environment where youll work with professionals across 80 countries and gain hands-on experience in the medical devices & pharmaceutical industry.
NewSr Regulatory Affairs Specialist - Global Markets Medtronic PlcSr Regulatory Affairs Specialist - Global MarketsMinneapolis, 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).
NewSr Regulatory Affairs Specialist - Global Markets MedtronicSr Regulatory Affairs Specialist - Global MarketsMinneapolis, MinnesotaIf 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).
Regulatory Specialist (Exempt) Government of the Virgin IslandsRegulatory Specialist (Exempt)Saint Croix, VIWork is performed in accordance with established policies but use of good judgement and independent decision-making is required in the application consulting, enforcement of rules and regulations/licensure laws. An employee in this class is responsible for ensuring compliance and recommending appropriate licensure and certification of childcare facilities.
Product Regulatory Specialist Lubrication Technologies IncProduct Regulatory SpecialistNew Hope, MN$75,000–$86,000 / yearAssists with ensuring products marketed meet regulatory requirements related to GHS, USMCA, Import/Export regulations, REACH and other regulatory entities as required. With a purpose to make tomorrow a little bit better than today for each other, our customers, and our communities, Ascentek provides an environment where you can love what you do and be your best every day.
Regulatory Compliance Specialist Pentair PlcRegulatory Compliance SpecialistNew Brighton, MN$61,200–$113,600 / yearFrom our residential water filtration to industrial water management to pool products and more, our 9,000 global employees serve customers in more than 150 countries, working to help create a better world for people and the planet through smart, sustainable water solutions. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, work location, and other relevant business or organizational needs.
NewPermitting & Regulatory Compliance Specialist II Core States GroupPermitting & Regulatory Compliance Specialist IIMNRemoteHEALTHCARE - Competitive health benefits including HSA with employer contribution, life insurance options, and supplemental coverage options, giving you the flexibility to select the coverage that best fits your needs and lifestyle. Core States Group designs, builds, and manages programs and projects across North America and has been recognized on top lists throughout the architecture, engineering, and construction (A/E/C) industry.
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).
AVP, Federal Regulatory Affairs Xcel Energy IncAVP, Federal Regulatory AffairsMinneapolis, MN$220,000–$278,900 / yearLead enterprise-wide engagement with Commercial Operations, Transmission, Integrated System Planning, Operating Companies, Legal, Regulatory, and other internal stakeholders on federal regulatory issues affecting transmission service, wholesale power transactions, organized wholesale market rules and trading strategies, generator interconnections, open access transmission policies, RTO participation, and transmission and wholesale business decisions. Provide strategic leadership and subject matter expertise on federal regulatory, wholesale market, transmission, reliability, tariff, and compliance matters before the Federal Energy Regulatory Commission (FERC), North American Electric Reliability Corporation (NERC), NERC Regional Entities, Regional Transmission Organizations (RTOs), and other regional organizations.
Senior Regulatory Affairs Spec Medtronic PlcSenior Regulatory Affairs SpecMNThe 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.
Principal Regulatory Affairs Spec ; Pelvic Health Medtronic PlcPrincipal Regulatory Affairs Spec ; Pelvic HealthMinneapolis, 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.