• Quality Technician

    Actalent (Cranberry, PA)


    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 solid understanding of medical device standards. You will work closely with Quality Engineers and Production teams to proactively identify compliance gaps, verify documentation, and support continuous improvement initiatives. This position plays a pivotal role on the floor in supporting daily operations and manufacturing execution.

    Responsibilities

    + Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like 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 reinforcing 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 in inspecting critical or high-precision components and/or 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

     

    This position is for the 2nd shift, working from 4:30pm to 3am.

     

    Job Type & Location

     

    This is a Permanent position based out of Cranberry, PA.

    Pay and Benefits

    The pay range for this position is $52000.00 - $66500.00/yr.

     

    All of Cadence’s medical plans offer:• Comprehensive, affordable coverage for a wide range of healthcare services.• Flexibility to see any provider you want, although you’ll savemoney when you stay in-network.• Free in-network preventive care, with services such as annualphysicals, recommended immunizations, well- woman andwell-child exams, flu shots, and routine cancer screeningscovered at 100%.• Prescription drug coverage is included with each medical plan.• Financial protection through annual out-of-pocket maximumsthat limit the amount you’ll pay each year.• Choice of five coverage levels: Employee Only, Employee +Spouse, Employee + Child, Employee + Children, or Family.

     

    Workplace Type

     

    This is a fully onsite position in Cranberry,PA.

     

    Application Deadline

     

    This position is anticipated to close on Dec 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.