• Lead QC Technician - 2nd shift

    ThermoFisher Scientific (Allentown, PA)


    Work Schedule

     

    Second Shift (Afternoons)

     

    Environmental Conditions

     

    Adherence to all Good Manufacturing Practices (GMP) Safety Standards

    Job Description

    Quality Inspector – cGMP Operations

    **Location:** US -Allentown, PA

    **Company:** Thermo Fisher Scientific

     

    At Thermo Fisher Scientific, you’ll join a team of 100,000+ professionals united by a mission—to enable our customers to make the world healthier, cleaner, and safer. Those who are passionate about quality, excel in regulated environments, and seek to make a meaningful impact through their work are encouraged to apply.

    Position Summary

    The Quality Inspector supports cGMP manufacturing operations by performing material inspections, documentation reviews, and activities dedicated to meeting regulatory standards. This role ensures that materials, components, and processes meet quality and regulatory requirements while supporting continuous improvement across operations.

    Key Responsibilities

    + Apply current Good Manufacturing Practices (cGMP) across all tasks.

    + Perform specifications approvals, Incoming Inspections, and distribution shipment reviews.

    + Conduct material and process inspections, including sampling activities.

    + Review and approve Packaging Electronic Production Orders.

    + Support root cause investigations and continuous improvement initiatives.

    + Author, revise, and follow SOPs and Work Instructions; ensure accurate documentation.

    + Escalate potential quality or compliance issues to leadership.

    + Ensure timely issue resolution and implementation of corrective actions.

    + Maintain a safe, compliant, and efficient working environment.

    + Perform additional duties as assigned to support business needs.

    Qualifications

    + Associate degree **or** High School Diploma with 2 years of relevant experience.

    + Minimum 1 year of experience in a pharmaceutical or other regulated industry.

    + Familiarity with key Quality Systems (Change Control, Deviations, Complaints, Documentation Management).

    + Ability to read, understand, and follow SOPs and Work Instructions in a GMP setting.

    + Strong attention to detail and ability to work both independently and on cross-functional teams.

    + Willingness to work various shifts, including overtime, as business needs require.

    Work Environment & Physical Requirements

    + Extensive standing and walking on the packaging floor.

    + Ability to lift up to 25 lbs occasionally and 10 lbs regularly.

    + Work in refrigerated (2–8°C) and freezer (-20°C) environments with provided PPE.

    + Exposure to atmospheric conditions requiring specialized protective equipment.

    + Must meet visual acuity and color-vision standards for inspection of products, components, and labels.

     

    Why Thermo Fisher Scientific?

     

    + Meaningful work that directly impacts global health and safety.

    + Industry-leading career development and training opportunities.

    + Inclusive, diverse, and mission-driven culture.

    + Competitive benefits and growth pathways.

     

    Apply Today

     

    Be part of a team that’s making a difference.

     

    **Apply now:** http://jobs.thermofisher.com

     

    Thermo Fisher Scientific is an EEO/Affirmative Action Employer. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.

     

    Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.