Regulatory Affairs Specialist III
Experis
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 & Product Stewardship department supporting cross‑functional teams. The ideal candidate will demonstrate strong scientific judgment, excellent communication skills, and a proactive approach to problem‑solving, which will align successfully in the organization. Job Title: Regulatory Affairs Specialist III Location: Maplewood, MN 55119 (Hybrid) Pay Range: $45-55/hr on W2 (No C2C) Job Type: 18-month Contract with potential for hire or extension Schedule: Monday-Friday 8am-5pm Central (flexible) Responsibilities Develop and implement global regulatory strategies supporting product commercialization and lifecycle management. Interpret emerging global regulations and communicate their impact to various stakeholders. Support regulatory submissions, product registrations, and compliance documentation processes. Lead product stewardship activities, including hazard, exposure, and risk assessments throughout the product lifecycle. Collaborate with R&D, Quality, Manufacturing, and other departments to ensure regulatory compliance and support new product development. Qualifications Bachelor’s degree in Chemistry, Biology, Chemical Engineering, or related scientific discipline. Minimum of five (5) years of experience supporting global regulatory compliance programs. Experience working with cross‑functional technical teams and managing multiple priorities. Strong understanding of global chemical and product safety regulations such as TSCA, REACH, GHS, RoHS, and FDA requirements. Excellent written and verbal communication skills, with the ability to influence and collaborate across diverse teams. Benefits Opportunity to work in a dynamic, innovative environment committed to making a positive impact on health and safety. Engage in meaningful projects that support sustainable product development and regulatory compliance. Collaborate with a diverse and talented team dedicated to continuous improvement and professional growth. Participate in industry‑leading initiatives and stay current with evolving global regulations. Be part of a company that values performance, quality, and innovation, fostering a supportive workplace culture. Consultant Benefits Medical and Prescription Drug Plans Dental Plan Vision Plan Health Savings Account Health Flexible Spending Account Dependent Care Flexible Spending Account Supplemental Life Insurance Short Term and Long Term Disability Insurance Business Travel Insurance 401(k) with Match Weekly Pay #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
$45 - $55 per hour
...sciences and filtration innovator in Maplewood, MN, for a high‑impact, 18‑month contract opportunity. We are seeking a Regulatory Affairs Specialist III to lead global compliance and product stewardship initiatives for a diverse portfolio of filtration, purification, and...SuggestedHourly payContract workTemporary workWork experience placement- ...Job Description Job Description Job Title: Regulatory Affairs Specialist III Location: Maplewood MN 55119 Duration: 18 months Virtual interview, Monday thru Friday, 8:00-5:00, Can be flexible on work hours, Hybrid on site When you're part of Thermo Fisher...SuggestedMonday to FridayFlexible hours
- ...Regulatory Affairs Specialist II - (RAS2.1) Company Description Stereotaxis is the global leader in innovative robotic technologies designed to enhance... ...highly preferred. Knowledge of global Class I, II and/or III hardware/software/sterile medical device requirements....SuggestedWork at office
$89.83k - $170.21k
...Actuarial Analyst III Location: This role requires associates to be in-office 1-2 days per week, fostering collaboration and... ...initiatives. Assists in training of actuarial trainees, analysts and specialists. Coordinates/directs special actuarial projects. Minimum...SuggestedTemporary workTraineeshipWork experience placementWork at officeLocal area2 days per week1 day per week- ...fully remote and hybrid career options; so, when you work for Northteq, you can work from anywhere! POSITION SUMMARY The Project Manager III is a mid-level role. You will lead Northteq teams through the implementation of our loan/lease origination software. In this role,...Permanent employmentFull timeCasual workWork at officeImmediate startRemote workMonday to Friday
$110.18k - $120k
...Regulatory Affairs Specialist – Fridley Position Summary The Regulatory Affairs Specialist is responsible for initiating global regulatory strategies for new products and post-market changes. They review post-market changes for devices currently marketed to determine regulatory...Full time- ...processes. 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 2...
- Job Duties Work Setup: Primarily onsite (flexibility for ~3 remote days/month) We’re looking for an experienced IT Project / Program Manager to lead cross-functional initiatives across business and technology teams. This role will drive delivery across multiple workstreams...Full timeFor contractorsRemote workShift work
$102.55k - $126.68k
...Financial Analyst III page is loaded## Financial Analyst IIIremote type: Hybridlocations: Minneapolis, MNtime type: Full timeposted on: Posted Yesterdayjob requisition id: JR103194**Your opportunity**:The Financial Analyst III is responsible for preparing, reviewing, consolidating...Work experience placementWork at office- Qualifications: Bachelor's degree in Computer Science, Information Systems, Business Administration, or other related field or equivalent work experience Typically requires 5 or more years of IT work experience, including a minimum of 2 years of demonstrated competency...For contractorsWork experience placement
- ...Senior Regulatory Affairs Specialist – Medical Devices About the Role We are seeking a Senior Regulatory Affairs Specialist to support global regulatory activities for medical devices. This role partners with cross‑functional teams to develop regulatory strategies, prepare...
$50 - $53 per hour
...Job Title: Senior Regulatory Affairs Specialist Location: 1225 Old Highway 8 NW, Saint Paul, MN 55112 Duration: 6 Months Work Arrangement: 100% Onsite Pay Range: $50 - $53 per hour (W2) We are seeking a Senior Regulatory Affairs Specialist to join one of our leading healthcare...Hourly payWork at office- ...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
- ...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...
$142.8k - $196.35k
...Principal Regulatory Affairs Specialist – Solventum Impact You’ll Make in this Role Serve as regulatory affairs lead on cross‑functional teams, owning product‑line regulatory submissions and registrations for the Dental Solutions business in global markets. Drive regulatory...Remote workWork visaFlexible hours$102.1k
...Principal Regulatory Affairs Specialist - Advertising & Promotion Onsite Location(s): Arden Hills, MN, US, 55112 Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you...Hourly payWork at officeLocal areaShift work3 days per week$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$25 - $27 per hour
...The Science Team at Russell Tobin and Associates is hiring a "Regulatory Specialist" for a top leading organization. Job Description This role involves working with regulatory affairs personnel across 80+ countries who are responsible for registering or re-registering...Contract workLocal area- IT Compliance Analyst Little Canada MN 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) in Little Canada MN is looking for hardworking, motivated talent...Contract work
$25 - $30 per hour
...Our client, a leader in the healthcare industry, is seeking a Regulatory Specialist to join their team. As a Regulatory Specialist, you will be part of the Regulatory Affairs department supporting global registration and re-registration processes for medical devices and...Weekly payTemporary workWork at officeLocal areaFlexible hours$87.03k - $138.97k
...BUSINESS SYSTEMS ANALYST III - CM WHAT IS THE OPPORTUNITY? Support the Capital Markets... ...the development, maintenance, training, regulatory compliance and support of all processes... ...in outside civic and community affairs, business and industry-related organizations...Work experience placementRemote work- ...We are looking to fill a Scientist II or III - Metrology Specialist position working as a full-time employee of Parexel FSP on long-term assignment... ...equipment during audits Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures...Full time
$70.1k - $87.6k
ABOUT THE ROLE This role is focused on providing project management assistance to a leadership team onsite at a project management office (PMO). This role may aid in mentoring our people, advancing the quality of our work, integrating our range of design services, managing...Contract workFor contractorsWork experience placementWork at officeFlexible hours$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- ...company strategic objectives. Responsibilities Identify opportunities to increase efficiency, improve service levels and to ensure regulatory compliance through enhanced operations Develop strategies to realize improvement opportunities, and ensure organizational...Full timePart timeWork at officeRemote workFlexible hours
$61.2k - $113.6k
...create a better world for people and the planet through smart, sustainable water solutions. We have an opportunity for a Regulatory Compliance Specialist to join our New Brighton, MN team. You will coordinate and perform third‑party listings for products produced...Full time$61.2k - $113.6k
...Job Overview Pentair is seeking a Regulatory Compliance Specialist in New Brighton, MN to coordinate third‑party product listings and ensure compliance with global regulations such as UL, CSA, and NSF. Responsibilities Coordinate and organize product regulatory test plans...Price workFull time- ...from regional & global functions: Data Providers/Approvers and Clients (Marketing/Business, Division, Plants, Requestors, Regulatory/Technical Affairs, Customer Service, Legal, R&D, Quality, etc.) # Identifies areas for service & quality improvements and leads or...Contract workLocal areaRemote work
- ...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
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