Regulatory Affairs Specialist
Indotronix International Corporation
Schedule - Monday - Friday work hours typically 8:00 am and 5:00 pm
As a Regulatory Affairs & Product Stewardship Associate within the Filtration & Separation business, you will support regulatory and product stewardship activities for a diverse portfolio of filtration, purification, bioprocessing, and life sciences products. This position plays a critical role in helping ensure products remain compliant, safe, and sustainable throughout their lifecycle while supporting business growth, innovation, and customer success. You will also play a key role in maintaining accurate, complete, and reliable product composition information used to support regulatory compliance, product stewardship, customer requirements, and product lifecycle management. The role combines regulatory and product stewardship knowledge with strong data management discipline.Key Responsibilities
Product Stewardship
• Support product stewardship activities throughout the entire product lifecycle
• Assist in conducting product hazard, exposure, and risk assessments
• Maintain product composition records, including material, substance, component, and related product attributes, in accordance with established business and regulatory requirements.
• Coordinate creation, update, review, approval, and retirement of composition records throughout the product lifecycle.
• Partner with Product Stewardship, Regulatory, R&D, Engineering, Quality, Operations, Supply Chain, and other functions to obtain and validate source information.
• Assist in developing mitigation strategies that balance regulatory compliance, customer expectations, and business objectives
• Support responsible chemical management and sustainable product design initiatives Regulatory Strategy & Compliance
• Support regulatory guidance activities throughout product development, change management, and product discontinuation activities
• Assist in ensuring compliance with applicable global chemical, environmental, product safety, and industry-specific regulations
• Assist with regulatory submissions, product registrations, declarations of conformity, and compliance documentation where applicable Global Regulatory Compliance
Develop knowledge and support compliance with applicable regulations including, but not limited to:
• TSCA
• REACH and UK REACH
• GHS and CLP
• RoHS
• Proposition 65
• PFAS regulations
• Food Contact regulations
• Biocide regulations
• Chemical inventory requirements
• Hazard Communication standards
• FDA and USP requirements, where applicable Cross-Functional Collaboration
Partner closely with:
• Research & Development
• Quality
• Manufacturing
• Operations
• Environmental Health & Safety
• Supply Chain
• Procurement
• Marketing
• Legal
to support regulatory compliance while supporting business objectives and operational excellence. Customer & Commercial Support
• Assist in responding to customer regulatory inquiries
• Support preparation of compliance letters, declarations, certificates, and technical documentation Minimum Qualifications
• Bachelor's degree in Chemistry, Chemical Engineering, Biology, Toxicology, Environmental Science, Materials Science, Life Sciences, Engineering, or another related scientific discipline
• 3-5 years of experience in Regulatory Affairs, Product Stewardship, Environmental Health & Safety, Product Compliance, Quality, or related technical functions (internships and co-op experience may be considered)
• Experience working with structured product, material, chemical, or composition data in enterprise systems.
• Demonstrated interest in regulatory compliance programs
• Ability to work effectively 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 or coursework related to filtration, purification, laboratory, bioprocessing, diagnostics, medical device, pharmaceutical, or chemical products
• Basic knowledge of global chemical regulations including TSCA, REACH, GHS, CLP, RoHS, PFAS, Food Contact, and Hazard Communication requirements
• Exposure to 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 Competencies
Successful candidates demonstrate:
• Strong scientific and technical aptitude
• Excellent problem-solving and analytical skills
• Customer-focused approach
• Ability to collaborate effectively across global organizations
• Strong relationship-building skills
• Effective communication with technical and non-technical audiences
• Continuous learning mindset
• Ability to balance compliance, innovation, and business objectives
Physical Requirements
Primarily office-based with occasional laboratory or manufacturing environment interaction. Occasional domestic and international travel (0-20%) may be required.
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Regulatory Affairs Specialist in Saint Paul, MN vacancy
$38 - $56 per hour
...LHH Recruitment Solutions is seeking a Regulatory Affairs Specialist for a minimum 6-month remote contract opportunity. This position is open to candidates residing in California who have prior experience in the medical device industry. The ideal candidate will have a...SuggestedHourly payContract workLocal areaImmediate startRemote workMonday to Friday$60.8k - $91.2k
...Associate Regulatory Affairs Specialist The Cardiac Ablation team within the Electrophysiology Therapies operating unit is focused on disrupting the Electrophysiology (EP) market to be the number one arrhythmia care, cardiac mapping, and ablation solutions provider...SuggestedH1bWork at officeLocal areaImmediate startFlexible hours- ...QMS Consulting seeks a Regulatory Specialist with direct experience drafting federal rules for the a federal agriculture agency. The specialist will serve as a rulemaking subject matter lead for up to three proposed-rule efforts. Working with QMS analysts and federal...SuggestedPermanent employment
$60.8k - $91.2k
...we work together to engineer the extraordinary. This position will be based in Mounds View, MN. The ** Associate Regulatory Affairs Specialist** will work under the guidance of their manager and more senior regulatory specialists to provide support for the products...SuggestedFull timeH1bWork at officeLocal areaImmediate startFlexible hours- ...flexible on work hours, Hybrid on site Key Responsibilities Regulatory Strategy & Compliance • Develop and execute global... ...Product Introduction (NPI) • Participate as the Regulatory Affairs and Product Stewardship representative on global product development...SuggestedMonday to FridayFlexible hours
$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 contractorsWork experience placementWorldwideShift work$157.6k - $236.4k
...building a career grounded in purpose, growth, and impact.A Day in the LifeThe Sr. Principal Regulatory Strategy Specialist is an individual contributor within Global Regulatory Affairs responsible for supporting and partnering with Regulatory teams across the organization...Full timeH1bWork at officeLocal areaImmediate startFlexible hours$120k - $180k
...Lafayette, CO or Mounds View, MN and supports Robotics Surgery Technologies (RST) in the Surgical Operating Unit.The Principal Regulatory Affairs Specialist (Pr. RAS) provides regulatory leadership and strategic direction for the consumable product [CB2.1]portfolio within RST....Full timeH1bWork at officeLocal areaImmediate startFlexible hours- ...areas, extending our products into new geographies and high-growth adjacent markets.Under minimal supervision, the Senior Regulatory Affairs Specialist will plan, manage and implement regulatory submissions to the U.S. Food and Drug Administration (FDA), European Union...Hourly payWork experience placementWork at officeLocal areaRelocationRelocation packageShift work3 days per week
- ...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
- ...Senior Regulatory Affairs Specialist At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the...Work at officeLocal area3 days per week
$120k - $180k
...Lafayette, CO or Mounds View, MN and supports Robotics Surgery Technologies (RST) in the Surgical Operating Unit.The Principal Regulatory Affairs Specialist (Pr. RAS) provides regulatory leadership and strategic direction for the consumable product (CB2.1)portfolio within RST....Full timeH1bWork at officeLocal areaImmediate startFlexible hours$120k - $180k
...Principal Regulatory Affairs SpecialistCareers that change lives start here. Medtronic is a global leader in healthcare technology with a... ...the Surgical Operating Unit. The Principal Regulatory Affairs Specialist (Pr. RAS) provides regulatory leadership and strategic direction...H1bWork at officeLocal areaImmediate startFlexible hours$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 officeLocal areaImmediate startFlexible hours- Job-ID32758545Reference26-01317Remote50% Remote 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...Remote work
- ...and efficiently.Responsibilities:• Coordinate HR compliance activities and project timelines to support organizational policy and regulatory requirements.• Review, organize, and maintain employment documentation to help ensure accurate and timely recordkeeping.• Monitor...Contract 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
$62k - $83k
...Compliance Specialist Job Locations US-MN-Eagan ID 2026-10863 Department Enterprise Risk Management... ...programs by managing day-to-day compliance activities, maintaining regulatory and program documentation, analyzing safety performance, and...Work at office$58k - $65k
...! Position Summary: The Compliance Coordinator supports the agency in assigned areas of compliance to ensure all licensing and regulatory agency monitoring and reporting requirements are satisfied. Schedule/Location/Pay: Full-time, hybrid opportunity with frequent...Full timeHome officeShift work$31.73 - $38.46 per hour
...application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Compliance Specialist Full Time 30-40 Professional Saint Paul, MN, US Salary Range: $31.73 To $38.46 Hourly Purpose: The Compliance Specialist is...Hourly payFull timeWork at officeLocal area1 day per week$28 - $32 per hour
...Job Title: Regulatory Compliance SpecialistJob Description This role involves preparing global Safety Data Sheets (SDS) and chemical labels, supporting employees and customers on regulatory and hazard communications. You will work under experienced leadership to ensure...Contract workTemporary workMonday to Friday$60k - $90k
Job Description At Norton Rose Fulbright, people thrive because of a shared commitment to quality, unity and integrity. The highly regarded law firm consistently receives recognition from Great Place to Work and Top Workplaces, two companies that specialize in assessing...Full timeFor contractorsWork at officeRemote workWorldwideFlexible hours- ...the right things and do things right The primary purpose of this job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory approvals within the United States and International markets and ensure compliance...Full timeImmediate start
$120k - $180k
...the LifeLOCATION: Onsite at a US-based Medtronic facility. Preference for the person to work EST hours. The Medtronic Global Regulatory Affairs team is looking for a highly motivated and skilled individual to join our Clinical Research, Medical Science, and Regulatory...Full timeH1bWork at officeLocal areaImmediate startFlexible hoursShift work$70k - $90k
Safety Program Coordinator-Bilingual English-Spanish Village Green Landscapes is a locally owned and operated full-scale landscape company serving the Twin Cities metro area with office locations in Saint Paul, New Brighton, Brooklyn Park, and Savage. We provide...Full timeContract workWork at office$74.4k - $111.6k
...control conditions, and other nervous system disorders. The Regulatory Affairs function partners with product development, quality, clinical... ...four days per week in the office. The Regulatory Affairs Specialist supports regulatory strategy, submissions, approvals, and...Full timeH1bWork at officeLocal areaImmediate startFlexible hours- ...Position Summary: The Senior Regulatory Specialist works with Quality Assurance and R&D Teams to ensure product safety and the quality of all products. This position will ensure regulatory compliance with regulatory bodies, customers and QualiTech and Ellison. Focus...Hourly payLocal areaFlexible hours
$18 - $20 per hour
...Our client, a leading organization in the manufacturing and industrial sector, is seeking a Regulatory Specialist I to join their team. As a Regulatory Specialist , you will be part of the Regulatory Support Department supporting the Product Steward team. The ideal candidate...Weekly payContract workTemporary workFlexible hours- ...focus is to revolutionize the standard of care in neuromodulation to positively impact patient’s lives. As a Principal Regulatory Affairs Specialist, you will provide Regulatory Affairs support for product development, sustaining engineering projects and compliance...
- ...relationships with officials and community partners. The position requires a bachelor’s degree in a related field, experience in legislative affairs, and strong communication skills. On-site work in Saint Paul, MN with a comprehensive benefits package. #J-18808-Ljbffr...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Specialist. Be the first to apply!
Related searches
- regulatory officer Saint Paul, MN
- regulatory affairs specialist Saint Paul, MN
- aml compliance analyst Saint Paul, MN
- medicare compliance specialist Saint Paul, MN
- compliance analyst Saint Paul, MN
- regulatory specialist Saint Paul, MN
- regulatory compliance analyst Saint Paul, MN
- cybersecurity policy and compliance analyst Saint Paul, MN
- research compliance officer Saint Paul, MN
- compliance consultant Saint Paul, MN



