Quality Inspector – Drive Quality & Compliance in Manufacturing

Quality Inspector

About Us

Micropore Inc. is a specialty materials manufacturer that produces high-value life support adsorbents for military and medical applications. The company's CO₂ absorbents are on 80% of free-world submarines, and all new U.S. Navy SEAL combat diving rebreathers are integrating Micropore Absorbent Technology. The company's medical anesthesia product business is growing rapidly, and Micropore is expanding its team to support this growth.

Micropore's mission is to develop and manufacture products that make a difference in the lives of our customers, and our employees are our most valuable asset.

If you are looking to work with a great team in a fast-paced small company producing world-class products, and want to make an immediate impact, please submit your resume.

Position Summary

We are seeking a Quality Inspector to join our team and play a critical role in maintaining and improving our Quality Management System. Reporting to the Quality Manager but requires close collaboration with production, engineering, and regulatory teams, this position ensures compliance with ISO 9001:2015, ISO 13485:2016, Medical Device Single Audit Program (MDSAP), and CE standards for our medical device business. The Quality Inspector will conduct inspections, support audits, and work with internal teams and customers to uphold our high-quality standards.

Areas of Responsibility

• Ensure compliance with quality policies, regulatory requirements, and customer expectations.
• Support customer-facing quality programs, including customer audits and complaint resolution.
• Conduct inspection of incoming raw materials, verifying specifications through visual and measurement tests.
• Utilize standard measuring equipment such as calipers, micrometers, and height gauges.
• Collect, analyze, and present Statistical Process Control (SPC) data.
• Maintain accurate records of inspections, calibrations, and test results.
• Assist in defining and optimizing quality assurance procedures to improve efficiency while ensuring compliance.
• Provide internal auditing support for ISO 9001:2015 and ISO 13485:2016 standards.
• Communicate daily with the Quality Manager regarding progress, issues, and improvement opportunities.
• Train personnel on quality control procedures and best practices.
• Perform other related duties as assigned.
  
  

Capabilities And Skills

• 2 to 5 years of quality experience in the manufacturing sector.
• ISO 9001:2015 & ISO 13485:2016 internal auditor training is preferred.
• Proficient in Corrective and Preventive Actions (CAPA).
• Familiarity with international medical device standards such as MDSAP and CE (or willingness to learn).
• Strong technical and computer literacy, including proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook, SharePoint).
• Excellent communication, organizational, and interpersonal skills.
• Ability to work independently with minimal supervision and as part of a collaborative team.
• Flexible and open to change and constructive feedback.
• Must be able to lift up to 10-30 lbs. and stand/walk/work on the production floor for long periods.
• Must be a U.S. Citizen.
  
  

Job Type

• Full time, Hourly
• Pay: $18 to $24 per hour
• Expected Hours: 40 hours per week
  
  

Benefits

• 401(k) with company matching
• Medical, dental, and vision insurance
• STD and LTD insurance
• Life insurance
• Paid time off, 80 hours accrued bi-weekly
• Flexible spending account
  
  

Schedule

• 8-hour shift
• Monday to Friday
• Work Location: In-person
  
  

If you are looking for an opportunity to work with a great team in a dynamic environment, apply today!