Description

- Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like calipers, micrometers, vision inspection equipment, gauges, etc.

- Conduct functional tests and verify conformance to detailed specifications and tolerances

- Interpret engineering drawings, specifications, and work instructions

- Record and maintain accurate inspection data, including lot history and traceability records

- Support lot release, material review, and root cause analysis for nonconforming parts

- Participate in audits and provide complete, well-organized inspection documentation

- Assist in implementing corrective actions and reinforcing compliance with ISO 13485 and FDA regulations

- Ensuring adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements

- Nonconformance, CAPA, and Material Review Board Support

Additional Skills & Qualifications

- Minimum 3–5 years of quality technical experience in the medical device industry required.

- Proven experience inspecting critical or high-precision components and/or devices.

- Familiarity with ISO 13485, and Good Documentation Practices (GDP).

- Proficiency with inspection equipment and interpreting engineering drawings and GD&T.

- Experience using Excel, electronic QMS platforms (e.g., Minitab, ETQ, Master Control), and document control systems.

- Excellent attention to detail, organization, and communication skills.

Preferred Qualifications:

- CQI or CQT certification

- Experience with cleanroom manufacturing in a medical device setting.

- Working knowledge of SPC and data analysis tools such as Minitab.

- Familiarity with Failure Investigation techniques.

Pay and Benefits

The pay range for this position is $52000.00 - $70000.00/yr.

Health Insurance
Dental Insurance
Vision Insurance
Disability Insurance (likely includes both short- and long-term)
401(k) Retirement Plan
Variable Compensation Plan (performance-based bonuses or incentives)

Workplace Type

This is a fully onsite position in Providence,RI.

Application Deadline

This position is anticipated to close on Aug 4, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.