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$142k - $238k
...industry.If you want to learn more about us, visit us at And for a full listing of open job opportunities go to The Position:The Certification Compliance Engineer serves as the technical authority for certification compliance on aircraft integration STC projects. Holding...SuggestedHourly payContract workFlexible hours$117.04k - $156k
...Purchasing lead for annual regulatory audits (e.g. FDA, TUV, ISO)• Identify potential supply chain risks and offers creative solutions... ...plus• Travel up to 10% of the time is required• APICS and ISM Certifications are preferredSalary range - $117,040.00 - $156,000.00 (...SuggestedFull time$147.54k - $182k
...evidence in a regulated product development environment (FDA QSR / ISO 13485 QMS preferred)Experience with CVE/NVD triage and... ...environments relevant to connected medical devicesRelevant security certification (e.g., CISSP, CISM, CEH, CompTIA Security+, or equivalent) is preferred...SuggestedFull time- ...international and local mandates like FDA regulations, ICG-GCP, and ISO 14155.Documentation and Execution:• Maintain integrated... ...investigator community relationships in aesthetics.• Industry certifications such as CCRP (Certified Clinical Research Professional) or ACRP...SuggestedTemporary workLocal areaFlexible hours
$155k - $170k
...The Opportunity As a modern technology consulting firm, ISO is at the forefront of change. We strengthen our clients with... ...college or university in a technology based field, or comparable certifications/education or equivalent field experience. Valid driver's license...SuggestedLocal areaRelocationNight shift- ...MDR) Risk Management: Conduct and update risk assessments per ISO 14971. Maintain and update: Risk Management Files (RMF). Hazard... .... Familiarity with post-market surveillance systems. Six Sigma / Quality certifications. Understanding of ultrasound imaging technology.Suggested
$94k - $150k
...understanding of relevant regulations and standards (FDA QSR, ISO 13485, ISO 14971, IEC 62304, and other applicable regulations and... ...in a science, engineering, or health-related discipline. RAPS certification is a plus.You must be able to successfully perform the following...SuggestedFull timeWork at officeImmediate startWork visaRelocation package3 days per week$109k - $150k
...participates in meetings. Summary of Education, Experience & Certification Bachelor’s degree in Business Administration, Legal Studies, Public... ...with contract management systems. Industry knowledge of ISO 9001 initiatives and processes preferred. Strong familiarity with...SuggestedPermanent employmentContract workShift work$120k - $170k
...unable to meet this requirement, we kindly ask that you do not apply. The Opportunity As a modern technology consulting firm, ISO is at the forefront of change. We strengthen our clients with technology solutions that help them boost performance, streamlines...SuggestedLocal areaRelocationNight shiftISOutsource
Bothell, WA23 days ago- ...Demonstrate attention to detail and strong record keeping skills, preferably in a regulated manufacturing environment (FDA cGMP/QSR or ISO experience is a plus). Possess good manual dexterity, eyesight, and ability to use a microscope for assembly tasks. Are...SuggestedTemporary workLocal areaMonday to FridayDay shift
Kelly Services
Bothell, WA9 days ago $100k - $150k
...Working knowledge of regulatory frameworks (PCI-DSS, HIPAA, SOC 2, ISO 27001). Strong scripting skills (Python, Bash) and Terraform... ...Preferred Qualifications Oracle Cloud Security Professional certification. CISSP, CCSP, or equivalent industry security certifications...SuggestedFull timeH1bLocal areaImmediate startRemote workVisa sponsorship- ...verification and validation. Worked a live FDA 483 or warning letter remediation and can describe what you personally closed. Fluent in ISO 14971, ISO 13485, and 21 CFR 820.30 Decompose requirements, author DFMEA and Usability FMEA, and design verification protocols...Suggested3 days per week
- ...quality into product design. Responsibilities: Design Control: Ensure compliance with Design Control requirements (21 CFR Part 820 / ISO 13485) throughout product lifecycle. Participate in design planning, design reviews, and design verification/validation activities. (...Suggested
$115k - $182k
...regulated industry (medical devices desirable, along with knowledge of Product Lifecycle Management, FDA Quality System Regulations and ISO 13485).Practical CAD experience, Creo preferred.You have a Bachelor’s degree—in Mechanical Engineering is preferred.You must be able...SuggestedFull timeWork at officeImmediate startWork visaRelocation package3 days per week$149.06k - $184.72k
...with Systems Engineering standards such as INCOSE • Experience with Medical Device Development and Risk Management standards such as ISO 13485 and ISO 14971 is preferred• Ability to define project goals and delivery dates to meet deadlines in a fast-paced environment• Ability...SuggestedFull time$30.61 - $37.09 per hour
...be able to stand/walk for extended periods of time Must be able to work in a cleanroom environment and perform aseptic processing in ISO 5 biosafety cabinets (as assigned), which require gowning and personal protective equipment (PPE), including by not limited to:...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaImmediate startRemote workFlexible hoursShift workNight shiftWeekend workAfternoon shift- ...~0-2 years of experience in quality control or quality assurance roles ~ Knowledge of quality standards and methodologies (e.g., ISO 9001, Six Sigma, GMP) ~ Proficiency in inspection tools and measurement techniques ~ Strong attention to detail and analytical skills...Weekly payTemporary workFlexible hours
$22 per hour
...Demonstrate attention to detail and strong record keeping skills, preferably in a regulated manufacturing environment (FDA cGMP/QSR or ISO experience is a plus). Possess good manual dexterity, eyesight, and ability to use a microscope for assembly tasks. Are...Hourly payTemporary workMonday to FridayShift workDay shift$155.55k - $221.12k
...Skilled at developing applications on a variety of levels including bare metal systems, RTOS and embedded Linux• Working knowledge of ISO 13485, ISO 14971 and IEC 62304 standards and applying this to medical device development• Proven mastery of software engineering best...Full timeTemporary work- ...management, and manufacturing transfer. Working knowledge of medical device regulations and standards, including FDA 21 CFR Part 820, ISO 13485, ISO 14971, and applicable international regulatory requirements. Experience supporting risk management activities, including...
$95k - $120k
...disciplined in following established procedures/processes Must have technical writing skills to develop qualification plans and reports ISO, FDA or other regulated industry training and experience is highly desired Ability to interface with oversea manufacturers when...$30.61 - $37.09 per hour
...be able to stand/walk for extended periods of time Must be able to work in a cleanroom environment and perform aseptic processing in ISO 5 biosafety cabinets (as assigned), which require gowning and personal protective equipment (PPE), including by not limited to:...Immediate startShift workNight shiftWeekend workAfternoon shift$149k - $237k
...dentistry space highly preferred.Your skills include a strong of relevant standards and regulations for the medical device industry (ISO, IEC, etc.). You have strong knowledge and understanding of Health Hazard Evaluations, Issue Impact Assessments, and Risk-Benefit Analyses...Full timeWork at officeImmediate startWork visaRelocation package3 days per week- ...credit analysis, reward program, payment clearing & settlement, payment processing, IMPS Payment Services, reconciliation solution, ISO Messaging & POS semi‑ and fully‑integrated solutions. Utilizing mandates and switch specifications from domestic and international payment...Work experience placementLocal areaRemote work3 days per week
- ...product documentation. Develop verification and validation test protocols where evidence is missing, ensuring compliance with FDA and ISO design control requirements. Prepare and structure remediated documentation for migration from legacy systems (e.g., Windchill) into...
$134k - $186k
...Engineering, Science or equivalent. ASQ CQE, CRE, CQM or related certifications are a plus. ~5+ years of relevant experience in the field... ...Management and FMEA. ~ Preferred experience with EU-MDR, 21CFR820, ISO 13485, ISO 14971/TS 24971, IEC 60601, IEC 62366, IEC 62304,...Full timeWork at officeImmediate startRemote workWork visaRelocation package3 days per week- ...oriented with excellent time-management abilities. Working knowledge of laboratory equipment and regulatory requirements (e.g., GLP, GMP, ISO). Experience with working in a database tool: Computerized Maintenance Management System (CMMS) Effective communicator, both...Daily paidContract workWork at officeLocal area
$175k - $195k
...communication, and cross-functional collaboration skills.Experience operating in an ISO-13485 / FDA environment or similar regulated industry preferred.Oracle experience is a plus.Preferred Certifications:APICS CPIM, CSCP, or similar supply chain certification.Skills/Abilities:...Contract work$115k - $158k
...material declarations, supplier disclosures, SDS, and environmental certificates.Integration with Medical Device Regulatory & QMSCollaborate with Regulatory Affairs and Quality to ensure alignment with ISO 13485, design controls, and change management processes.Support...$119.1k - $186.3k
...to its principal business.Requisition SummaryPACCAR's Corporate Emission Compliance team is looking for an Emissions Compliance Certification Manager to provide leadership in executing PACCAR's emissions compliance strategy across engine and vehicle programs.Job Functions...Temporary work
