Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Regulatory Affairs Specialist III

Indotronix International Corporation

Monday thru Friday, 8:00-5:00, Can be flexible on work hours, Hybrid on site

Key Responsibilities
Regulatory Strategy & Compliance
• Develop and execute global regulatory strategies that support new product commercialization and lifecycle management.
• Interpret emerging global regulations and communicate regulatory impacts to business stakeholders.
• Provide regulatory guidance throughout product development, change management, and product discontinuation activities.
• Ensure compliance with applicable global chemical, environmental, product safety, and industry-specific regulations.
• Support regulatory submissions, product registrations, declarations of conformity, and compliance documentation where applicable.


Product Stewardship
• Lead product stewardship activities throughout the entire product lifecycle.
• Conduct product hazard, exposure, and risk assessments.
• Evaluate product composition for regulatory compliance and sustainability objectives.
• Partner with R&D and Product Management to identify regulatory risks early during product development.
• Develop mitigation strategies that balance regulatory compliance, customer expectations, and business objectives.
• Support responsible chemical management and sustainable product design initiatives.
Global Regulatory Compliance
Provide expertise in applicable regulations including, but not limited to:
• TSCA
• REACH and UK REACH
• GHS and CLP
• RoHS
• Proposition 65
• PFAS regulations
• Food Contact regulations
• Drinking Water regulations
• Biocide regulations
• Chemical inventory requirements
• Hazard Communication standards
• FDA and USP requirements, where applicable
New Product Introduction (NPI)
• Participate as the Regulatory Affairs and Product Stewardship representative on global product development teams.
• Support Stage Gate and design review processes.
• Review product claims, labels, instructions for use, technical literature, and marketing materials.
• Ensure regulatory requirements are incorporated into commercialization activities.
• Evaluate product changes for regulatory impact and coordinate required actions before implementation.
Cross-Functional Collaboration
Partner closely with:
• Research & Development
• Quality
• Manufacturing
• Operations
• Environmental Health & Safety
• Supply Chain
• Procurement
• Marketing
• Sales
• Legal
• Global Regulatory Affairs
to ensure regulatory compliance while supporting business objectives and operational excellence.
Customer & Commercial Support
• Respond to customer regulatory inquiries.
• Prepare compliance letters, declarations, certificates, and technical documentation.
• Support customer audits and regulatory assessments.
• Review customer questionnaires regarding product compliance and chemical content.
• Partner with Commercial teams to resolve customer regulatory concerns.
Regulatory Intelligence
• Monitor emerging global regulations affecting products and markets.
• Assess business impact and develop implementation strategies.
• Communicate regulatory changes to leadership and cross-functional teams.
• Participate in industry associations and professional organizations to maintain current regulatory knowledge.
Quality & Risk Management
• Support Quality Management Systems including ISO 9001 and ISO 13485 where applicable.
• Participate in product risk assessments and Failure Mode and Effects Analysis (FMEA) activities.
• Contribute to continuous improvement initiatives that strengthen compliance and operational effectiveness.
• Support internal and external audits.


Minimum Qualifications
• Bachelor's degree in Chemistry, Chemical Engineering, Biology, Toxicology, Environmental Science, Materials Science, Life Sciences, Engineering, or another related scientific discipline.
• Minimum five (5) years of experience in Regulatory Affairs, Product Stewardship, Environmental Health & Safety, Product Compliance, Quality, or related technical functions.
• Demonstrated experience supporting global regulatory compliance programs.
• Experience working in cross-functional technical teams.
• Excellent written and verbal communication skills.
• Strong analytical, organizational, and project management skills.
• Ability to manage multiple priorities within a fast-paced global environment.


Preferred Qualifications
• Experience supporting filtration, purification, laboratory, bioprocessing, diagnostics, medical device, pharmaceutical, or chemical products.
• Knowledge of global chemical regulations including TSCA, REACH, GHS, CLP, RoHS, PFAS, Food Contact, and Hazard Communication requirements.
• Experience supporting New Product Introduction (NPI) and product lifecycle management.
• Experience performing product risk assessments and lifecycle evaluations.
• Knowledge of ISO 9001, ISO 13485, and quality management systems.
• Experience preparing Safety Data Sheets (SDS), regulatory declarations, and customer compliance documentation.
• Regulatory Affairs Certification (RAC), Certified Hazardous Materials Manager (CHMM), or other applicable professional certifications.


Competencies
Successful candidates demonstrate:
• Strong scientific and technical judgment.
• Excellent problem-solving and risk assessment skills.
• Customer-focused decision making.
• Ability to influence without authority across global organizations.
• Strong collaboration and relationship-building skills.
• Effective communication with technical and non-technical audiences.
• Continuous improvement mindset.
• Ability to balance compliance, innovation, and business objectives.
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Regulatory Affairs Specialist III in Saint Paul, MN vacancy
  • $74.4k - $111.6k

     ...Regulatory Affairs SpecialistMedtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide...  ...satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.Physical Job RequirementsThe... 
    Suggested
    H1b
    Work at office
    Local area
    Immediate start
    Flexible hours

    Medtronic Plc

    Saint Paul, MN
    9 hours ago
  • $74.4k - $111.6k

     .... This position will be based in Mounds View, MN. The Regulatory Affairs Specialist assists in the development of strategies for worldwide product...  ...that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above... 
    Suggested
    H1b
    Local area
    Immediate start
    Remote work
    Worldwide
    Flexible hours

    Medtronic Plc

    Saint Paul, MN
    1 day ago
  • $74.4k - $111.6k

     ...This position will be based in Mounds View, MN. The Regulatory Affairs Specialist assists in the development of strategies for worldwide product...  ...that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above... 
    Suggested
    Full time
    H1b
    Local area
    Immediate start
    Remote work
    Worldwide
    Flexible hours

    Medtronic

    Saint Paul, MN
    3 days ago
  •  ...Senior Regulatory Affairs SpecialistWork mode: Hybrid Onsite Location(s): Marlborough, MA, US, 0...  ...individual for a Senior Regulatory Affairs Specialist position (hybrid work mode) supporting...  ...filings for new and modified Class III productsProvides technical reviews of test... 
    Suggested
    Work at office
    Local area
    Relocation
    3 days per week

    Boston Scientific

    Saint Paul, MN
    4 days ago
  •  ...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.... 
    Suggested
    Work at office

    Stereotaxis

    Minneapolis, MN
    4 days ago
  • $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... 
    For contractors
    Work experience placement
    Worldwide
    Shift work

    Abbott

    Saint Paul, MN
    8 hours ago
  •  ...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... 
    Worldwide

    Socket

    Saint Paul, MN
    23 hours ago
  • $85k - $95k

     ...Regulatory And Clinical SpecialistAs a global medtech company, we are...  ....The Regulatory and Clinical Specialist will support the clinical evaluation...  ...in medical device.Class III active-implantable experience...  ...medical device regulatory affairs or a Ph.D. with at least 3 years... 
    Remote work
    Worldwide

    LivaNova

    Minneapolis, MN
    3 days ago
  •  ...Regulatory Affairs SpecialistMedtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a range of medical devices focusing on a diverse line of Sutures (absorbable... 
    Flexible hours

    Minnesota Jobs

    Saint Paul, MN
    3 days ago
  •  .... • 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... 

    Insight Global

    Saint Paul, MN
    4 days ago
  •  ...Regulatory Affairs Specialist The Regulatory Affairs Specialist will assist in maintaining market authorizations for Scanlan products, including design files, technical documentation, product registrations and listings. They will also assist with post-market surveillance... 
    Work experience placement
    Work at office
    Worldwide

    Scanlan International, Inc.

    Saint Paul, MN
    1 day ago
  •  ...Regulatory Affairs Specialist This 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... 
    Work at office

    Oxenham Group

    Saint Paul, MN
    5 days ago
  •  ...growth adjacent markets.Under minimal supervision, the Senior Regulatory Affairs Specialist will plan, manage and implement regulatory submissions to...  ...medical device industry working with Class II and Class III medical devices. Proficiency with Microsoft Word, Excel and... 
    Hourly pay
    Work experience placement
    Work at office
    Local area
    Relocation
    Relocation package
    Shift work
    3 days per week

    Boston Scientific Corporation

    Arden Hills, MN
    8 hours ago
  •  ...We are looking to fill a Scientist II or III - Metrology Specialist position working as a full-time employee of Parexel FSP on long...  ...equipment during audits Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures... 
    Full time

    PAREXEL

    Saint Paul, MN
    2 days ago
  • $80.9k - $127.05k

     ...US-Nationwide-FIELD Full time 20186058 What Regulatory Affairs contributes to Cardinal Health Regulatory provides regulatory affairs...  ..., MA. Job Summary The Principal Regulatory Affairs Specialist supports the Medical Solutions Regulatory Affairs team by managing... 
    Full time
    Temporary work
    Work experience placement
    Local area
    Immediate start
    Remote work
    Flexible hours

    Cardinal Health

    Saint Paul, MN
    1 day ago
  •  ...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

    Braccomedtech

    Saint Paul, MN
    1 day ago
  •  ...impact patient’s lives. Reporting to the Sr. Director, Regulatory Affairs, the Senior Regulatory Affairs Specialist will provide input to global regulatory strategies...  ...Experience with Active Implantable and/or Class III medical devices Experience with Australian reimbursement... 

    Saluda Medical

    Minneapolis, MN
    1 day ago
  • $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 office
    Local area
    Immediate start
    Flexible hours

    Coloplast

    Minneapolis, MN
    8 hours ago
  • 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... 

    Katalyst Healthcares & Life Sciences

    Minneapolis, MN
    3 days ago
  • $107.7k - $131.3k

     ...based attack techniques. Experience in a regulated environment subject to requirements such as PCI DSS, SOX, or aviation-sector regulatory oversight. Experience supporting operational technology or specialized business systems in addition to corporate IT.... 
    Full time
    Part time
    Work at office
    Local area
    Visa sponsorship
    Shift work

    Allegiant

    Minneapolis, MN
    8 hours ago
  •  ...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... 
    Local area

    Javen Technologies

    Saint Paul, MN
    3 days ago
  •  ...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... 

    Russell Tobin

    Maplewood, MN
    5 days ago
  •  ...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, you... 
    Permanent employment
    Full time
    Casual work
    Work at office
    Immediate start
    Remote work
    Monday to Friday

    Northteq, Inc.

    Minneapolis, MN
    2 days ago
  •  ...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

    Russell Tobin

    Maplewood, MN
    5 days ago
  •  ...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

    Minneapolis, MN
    2 days ago
  • $105.63k - $130.49k

     ...level. We are more than products, we are a team of inspired people doing extraordinary things.YOUR OPPORTUNITYAs the Financial Analyst III/Sr. Financial Analyst you will support a growing custom manufacturing business by driving strategic financial analysis, operational... 
    Full time
    Work at office
    Worldwide

    Greenheck Group

    Minneapolis, MN
    2 days ago
  •  ...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... 

    RXinsider

    Minneapolis, MN
    4 days ago
  •  ...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 office
    Remote work
    Work from home
    Worldwide

    PAREXEL

    Saint Paul, MN
    5 days ago
  • $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 pay
    Temporary work
    Remote work
    Monday to Friday
    Flexible hours
    Shift work
    Day shift

    State of Minnesota

    Saint Paul, MN
    1 day ago
  • $35k - $48k

    Junior Compliance Officer (Operations, Jr. Analyst)The MIL Corporation seeks a Junior Compliance Officer (Operations, Jr. Analyst) to support a federal law enforcement client with I-9 audit support services and worksite enforcement compliance activities. The role assists...
    Full time
    Contract work
    For contractors
    Work at office
    Remote work
    Weekend work

    The MIL Corporation

    Saint Paul, MN
    5 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Regulatory Affairs Specialist III. Be the first to apply!