Quality Control Inspector (Chemistry)

Yoh Idibu

Saint Paul (MN)

Sur place

USD 36 000 - 39 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Medical benefits
Health Savings Account (HSA)
Life & Disability Insurance
EAP (Employee Assistance Program)
401K Retirement Savings Plan
Direct Deposit & weekly payroll
Referral bonuses
Training opportunities

Résumé du poste

Yoh is seeking a Quality Control Inspector (Chemistry) for a medical device manufacturer in St. Paul, MN. You will perform QC inspections, lab testing, and product acceptance for sterile and non-sterile devices, ensuring compliance with specifications and regulatory standards.

Responsibilities include reviewing records, preparing sterilization documentation, environmental monitoring, and coordinating MRB activities. Requires STEM degree and 3+ years in QC/inspection with MS Office proficiency.

Qualifications

  • Associate degree or higher in STEM required.
  • 3+ years of quality control/inspection in medical device manufacturing.
  • Experience preparing technical reports and documentation using MS Office.
  • Able to interpret blueprints, specs and procedures.
  • Working knowledge of analytical chemistry.

Responsabilités

  • Perform QC inspections (incoming, in-process, final) to verify specs.
  • Document inspection and testing results with high detail.
  • Review records, sterile processing docs, test results for compliance.
  • Collect and submit samples to labs and manage documentation.

Connaissances

Blueprint reading
Attention to detail
Communication skills
Analytical chemistry

Formation

Associate degree or higher in STEM
3+ years QC/inspection in medical device
MS Office documentation

Outils

Gauges
Micrometers
Calipers
Indicators
Comparators
Microscopes

Description du poste

Yoh is hiring a Quality Control Inspector (Chemistry) for our medical device manufacturing client in St. Paul, MN. In this role, you will be responsible for performing quality control inspections, laboratory testing, and product acceptance activities for sterile and non-sterile medical devices. The Quality Control Inspector (Chemistry) will ensure products meet approved specifications, procedures, customer requirements, and applicable regulatory standards while supporting manufacturing, laboratory, and quality operations.

Industry: Medical Device Manufacturing

Location: St. Paul, MN

Job Functions
  • Perform incoming, in-process, final, and finished product QC inspections to verify conformance to specifications, customer requirements, and quality system requirements.
  • Perform accurate measurements and document inspection and testing results with a high level of attention to detail.
  • Ensure inspections and testing activities are completed in accordance with production schedules and established priorities.
  • Review manufacturing records, sterile processing documentation, test results, certifications, labeling, and related paperwork for compliance with specifications and quality system requirements.
  • Support Warehouse associates to ensure materials are properly handled and stored according to specifications and quality system requirements.
  • Collect, prepare, and submit samples to internal and external laboratories.
  • Prepare sterilization documentation and analyze sterilization and biological indicator results.
  • Perform UV-Vis, FTIR, and basic wet chemistry testing and analyze results against established specifications.
  • Prepare and mix chemical formulations for Production and Manufacturing use.
  • Perform environmental monitoring activities, including temperature and humidity monitoring and controlled environment testing.
  • Identify, document, segregate, and quarantine nonconforming materials to prevent unintended use.
  • Assist with investigations involving products or processes suspected of being nonconforming.
  • Coordinate Material Review Board activities and support timely disposition of nonconforming materials.
  • Communicate with applicable stakeholders regarding materials awaiting MRB review, action, or disposition.
  • Maintain controlled access to QA Hold and Quarantine areas.
  • Inspect returned goods and ensure nonconforming materials are appropriately segregated.
  • Maintain the equipment calibration program to ensure production, test, and measurement equipment is calibrated by required due dates.
  • Verify equipment is appropriately identified with calibration status and remove equipment from service when calibration is expired or out of specification.
  • Verify preventive maintenance and equipment qualification activities are completed as required.
  • Assist with maintaining Quality Assurance work instructions in accordance with current regulations, standards, and quality system requirements.
Education
  • Licensure and/or Experience· Associate degree or higher in a STEM-related discipline required.
  • 3+ years of experience in quality control and inspection within a medical device manufacturing environment.
  • Experience preparing technical reports, analyses, and documentation using Microsoft Office.
  • Ability to interpret blueprints, technical documentation, specifications, and procedures.
  • Working knowledge of analytical chemistry.
  • Applied knowledge of quality control, inspection methodologies, and test and measurement instrumentation.
  • Experience using measurement and inspection instruments including gauges, micrometers, calipers, indicators, comparators, and microscopes.
  • Strong attention to detail with the ability to produce precise measurements, documentation, and quality records.
  • Excellent written and verbal communication skills with the ability to communicate effectively with auditors, suppliers, management, and cross-functional teams.
  • Excellent hand-eye coordination and visual acuity, including color vision, close vision, and the ability to identify fine details under magnification.

Estimated Min Rate: $26.00

Estimated Max Rate: $28.00

What’s In It for You?
  • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
  • Health Savings Account (HSA) (for employees working 20+ hours per week)
  • Life & Disability Insurance (for employees working 20+ hours per week)
  • MetLife Voluntary Benefits
  • Employee Assistance Program (EAP)
  • 401K Retirement Savings Plan
  • Direct Deposit & weekly epayroll
  • Referral Bonus Programs
  • Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice.

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