Job Description

Work Schedule

Second Shift (Afternoons)

Environmental Conditions

Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Work Schedule

Standard (Mon-Fri) - Second Shift

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, some degrees of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Quality Inspector – cGMP Operations

Location: US -Allentown, PA
Company: Thermo Fisher Scientific

At Thermo Fisher Scientific, you’ll join a team of 67,000+ 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.

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 assigned to support business needs.

Qualifications

Education:

High School Diploma OR GED Required

Experience:

• 3+ years of relevant experience
• Minimum 1 year of experience in a pharmaceutical or other regulated industry preferred
• 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.