QA Inspector - Second Shift

Thermo Fisher Scientific•Allentown, PA

1d•Onsite

About The Position

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.

Requirements

High School Diploma OR GED Required
3+ years of relevant experience
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.
Must meet visual acuity and color-vision standards for inspection of products, components, and labels.

Nice To Haves

Minimum 1 year of experience in a pharmaceutical or other regulated industry preferred
Familiarity with key Quality Systems (Change Control, Deviations, Complaints, Documentation Management).

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 assigned to support business needs.