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$77k - $92k
...balance multiple projects, demands and competing deadlines. Creates and maintains Design History files per internal company procedures, ISO 9001, ISO 13485 requirements and FDA Design Control (21 CFR 820) support as needed. Proactively manage changes in product and...SuggestedSummer workWork at officeErgotron
Eagan, MN25 days ago$142k - $167k
...Attend stakeholder meetings and provide real‑time legal insights. Support MISO’s involvement in FERC technical conferences and RTO‑ISO Council initiatives. Contribute to special projects, including Alternative Dispute Resolution and compliance filings. What We’re Looking...SuggestedFull time- ...and in a timely manner. Stay current with EPA and FDA Good Laboratory Practice Regulations (40 CFR Part 160 and 21 CFR Part 58) and ISO 17025 or other regulations as applicable. Proficiency with PC based software programs. Ability to write reports, business correspondence...Suggested
- ...testing, environmental monitoring, and method qualifications. This position plays a key role in executing testing within a cGLP and ISO 17025 environment, maintaining data integrity, and ensuring results are scientifically sound, timely, and defensible. The Principal Scientist...Suggested
$85.08k - $135.9k
...of reports as required, including departmental KPIs, safety and property damage incidents, and environmental reports. Participate in ISO 9001 internal audits. Handle internal UPS shipments and mail as needed. Coordinate plant supplies, carpet cleaning services, and...SuggestedTemporary workWork experience placementMonday to FridayFlexible hours$20 - $24 per hour
...precisely follow Standard Operating Procedures, global methods, local methods and published standard or compendia methods i.e. USP, ISO, ASTM. Understand and apply basic laboratory safety instructions, reagent handling precautions, and disposal of chemical waste according...SuggestedFull timeTemporary workWork at officeLocal areaMonday to Friday$100.36k - $150.8k
...for this role. Ability to travel up to 15% of the time. PREFERRED QUALIFICATIONS Medical Device experience. Working knowledge of ISO 13485 & ISO 9001. Knowledge of state‑of‑the‑art manufacturing technologies, including Manufacturing Execution Systems (MES) and automation...SuggestedMinimum wageLocal areaWorldwideVisa sponsorship- ...preferably SolidWorks) to create models, drawings, and layouts. - Ensure compliance with medical device regulations and quality systems (ISO, GMP, GLP). - Partner with Legal and IP teams to identify and support patent opportunities. - Drive innovation by integrating product...Suggested
$152k - $173k
...operations. What You’ll Bring 8+ years of real world/applied experience in the electric power industry, preferably with utilities, RTOs/ISOs, or control room grid operations. Proven experience applying electric power research in industry, academic, or lab settings with a...Suggested$80k
...experience or training desired in process modeling, process maturity models; quality improvement techniques such as 6 Sigma, Lean Sigma, or ISO 9000. Prior account management, sales, or sales support experience. Proficiency with Microsoft Products (Word, Excel, Access,...SuggestedFor contractorsWork at officeRemote workFlexible hours2 days per weekBlue Cross and Blue Shield of Minnesota
Eagan, MN14 hours agonew$115k - $134k
...engineering economics, economics, energy policy, or project management. Prior industry experience working for an Independent System Operator (ISO), Regional Transmission Operator (RTO), federal or state regulatory commission, Electric Reliability Organization (ERO), Regional...SuggestedLocal areaShift work$72.1k - $133.9k
...inventory control, and lifecycle tracking of equipment. Ensure adherence to security protocols and regulatory requirements (e.g., SOC 2, ISO 27001). Participate in capacity planning and contribute to strategic infrastructure decisions. Support audits and inspections while...SuggestedWork at officeLocal areaRemote workFlexible hours2 days per week3 days per week$99.4k - $184.6k
...Experience with virtualization technologies (VMware, Hyper‑V) and cloud infrastructure. Experience in managing audits and compliance (SOC, ISO, HIPAA, etc.). Strong knowledge with monitoring tools, DCIM platforms, and ticketing systems. Excellent analytical, problem‐solving...SuggestedWork at officeLocal areaFlexible hours2 days per week3 days per week- ...support where needed. Stay current with evolving global safety regulations, guidance, and standards; ensure compliance with FDA, EU MDR, ISO 14155, and other relevant frameworks. Documentation & Data Management Maintain accurate, complete, and confidential safety case...SuggestedTemporary workLocal areaFlexible hours
- ...Experience with virtualization technologies (VMware, Hyper-V) and cloud infrastructure. Experience in managing audits and compliance (SOC, ISO, HIPAA, etc.). Strong knowledge with monitoring tools, DCIM platforms, and ticketing systems. Excellent analytical, problem-solving...SuggestedWork at officeFlexible hours2 days per week3 days per week
- ...regulations and the principles of the EU Medical Device Directive (93/42/EEC) and Medical Device Regulation (2017/745), the FDA GMP, ISO-13485, Health Canada and their fundamental requirements.* Experience developing terminally sterilized medical devices, with an understanding...Hourly payWork at office
$72.1k - $133.9k
...provide recommendations for cost optimizations and efficiencies. Support, track, and manage security compliance (currently SOC2 type 2, ISO 27001, Cyber Essentials, Cyber Essentials Plus, and PCI SAQ‑D) and required processes for certifications. Keep current and comply...Casual workLocal areaRemote workFlexible hoursAfternoon shift- ...foodservice environments Familiarity with EOS, Lean Six Sigma or other Continuous Improvement methodologies Experience with SQF, BRC, or ISO 22000 certification programs Bilingual (English/Spanish) is a plus QA Certifications (Preferred) Certified Quality Auditor (CQA)...Work experience placementWork at officeLocal area
$72.28k - $105.04k
...tables, formulas, charting). Working knowledge of government and industry quality assurance codes and standards (e.g., 21 CFR 820, ISO 13485). Position requires up to 15 % travel. Preferred Requirements At least 2 years of industry experience in medical devices, drugs...Minimum wageWork experience placementLocal area$99.4k - $184.6k
...programs and resolving escalations with professionalism and urgency. Working knowledge of key frameworks and standards (e.g., SOC 2, ISO 27001, NIST, PCI, ITGC). Relevant industry certifications (e.g., CISSP, CISA, CISM, GSEC, ITIL) are highly desirable. Strategic,...Work at officeLocal areaFlexible hours2 days per week3 days per week- ...ISO 13485 Lead Auditor RQM+ is the MedTech CRO, accelerating innovation to patient impact. Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic...Contract work
- ...Quality Auditor ISO 9001 The Quality Assessments Division of Smithers seeks full-time Auditors to join our ISO Sector team. If you want to be a part of our mission to provide our clients with accurate data, on-time with high-touch, we'd love to have you on board....Full timeTemporary workWork experience placementFlexible hours
- ...Completing all opening and closing responsibilities as required. 9. Support operational activities such as floor sets, replenishment (ISOS), etc. 10. Participates in individual company trainings included but not limited to compliance, product, process, talent...Part timeSeasonal workWork at officeFlexible hoursNight shiftWeekend workAfternoon shift
- ISO 13485: 2016 Freelance Auditor - US Midwest 1 day ago Be among the first 25 applicants Medpoint is seeking certified ISO 13485: 2016l auditors to conduct contract supplier audits. Successful candidates will meet the following requirements: Experience auditing supply...Full timeContract workFor contractorsFreelance
$110k - $125k
...Senior Auditor, Certification Audits (IATF, ISO 16949) We are SGS the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices...Local areaImmediate startRemote workWeekend work- ...area It would be a plus if you also possess previous experience in: ~ Experience in a regulated industry preferred (e.g. FDA, ISO) Beckman Coulter Diagnostics, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs...Hourly payRemote workWork from homeFlexible hours
Beckman Coulter Diagnostics
Chaska, MN15 days ago $165k - $180k
...when dealing with engineered products. Experience managing production within a Quality Management System, holding certifications (QMAS, ISO, NadCap, IPC, etc.), and having a proven track record of leading Lean manufacturing improvements, implementing and sustaining 5S, Six...Temporary workImmediate startFlexible hoursAll Flex Solutions
Bloomington, MN10 days ago- ...or regulated product environment). Skills / Competencies In-depth knowledge of regulatory frameworks (e.g. FDA, Health Canada, ISO 13485, IEC standards, etc.). Strong technical writing skills, ability to compile regulatory dossiers. Excellent analytical and...Work at office
Orion Talent
Minneapolis, MN8 days ago - ...experience in Quality Engineering within aerospace, defense, or a regulated manufacturing environment ~ Working knowledge of AS9100 or ISO 9001 standards ~ Strong analytical, communication, and problem-solving skills ~ Ability to work independently and collaboratively...Weekend workAfternoon shift
Excelion Partners
Chaska, MN10 days ago $90k - $105k
...Monitor equipment and chart the course for continuous improvement of OEE and maintenance processes for compliance with Company, FDA, ISO, OSHA, and Good Manufacturing Practices (GMP) regulations. • Ensure completion of continuous improvement projects related to the automated...Beckman Coulter Diagnostics
Chaska, MN22 days ago
