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Job Title: Quality TechnicianJob Description

The Quality Technician is responsible for performing detailed inspections and functional tests on critical components and finished medical devices. This role demands precision, consistency, and a strong understanding of medical device standards. The technician will closely collaborate with Quality Engineers and Production teams to identify compliance gaps, verify documentation, and support continuous improvement efforts. This position is active on the floor, supporting daily operations and manufacturing execution.

Responsibilities

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

+ 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 reinforce compliance with ISO and FDA regulations.

+ Ensure adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements.

+ Support nonconformance, CAPA, and Material Review Board activities.

Essential Skills

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

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

+ Familiarity with ISO standards 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.

Additional Skills & 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.

Work Environment

The work environment involves active participation on the manufacturing floor, with a focus on supporting daily operations and manufacturing execution. The role requires adherence to strict medical device standards and practices, including ISO and FDA regulations. Quality technicians will engage with various inspection tools and electronic platforms to ensure precision and compliance.

Pay and Benefits

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

Health InsuranceDental InsuranceVision InsuranceDisability Insurance (likely includes both short- and long-term)401(k) Retirement PlanVariable Compensation Plan (performance-based bonuses or incentives)

Workplace Type

This is a fully onsite position in Cranberry,PA.

Application Deadline

This position is anticipated to close on Aug 5, 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 [email protected] (%[email protected]) for other accommodation options.