Jobs and Careers

In Process Inspector 2 - Finishing Operations, 2nd Shift

Thermo Fisher Scientific

United Statesfull_timeVerifiedPosted 18 May 2026

💰 $52,000/yr($48,000/yr – $52,000/yr)

About the role

Work Schedule

Second Shift (Afternoons)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Warehouse, Will work with hazardous/toxic materials

Job Description

Shift Schedule: 2nd Shift 03:00pm - 11:30pm
Pay Range: $24-$26

The In Process Inspector role has a significant impact in ensuring the quality and integrity of the production process. Their responsibilities include monitoring and inspecting the various stages of manufacturing to identify any discrepancies while using automatic equipment or visually inspecting labels. Their vigilance and attention to detail play a crucial role in preventing defects, ensuring product safety, and maintaining overall process efficiency.

A Day in the Life:

Conducting inspections using automatic inspection equipment: Operates and monitors automatic inspection equipment to assess the quality and integrity of pharmaceutical labels during the manufacturing process including setting up the equipment, conducting routine checks, and interpreting the results to identify any defects or change requests from specifications. Ensures that labels meet the required standards for accuracy, legibility, and adherence to regulatory requirements
Performing QC inspections: Conducts Quality Control (QC) inspections at various stages of the manufacturing process including visually examining labels, verifying label content, conducting accurate counts, checking for proper alignment, and assessing print quality. Uses appropriate tools and techniques, to ensure that labels meet the necessary quality standards and complies with regulatory guidelines.
Documenting and reporting findings: Records all inspection results and documents any non-conformities or deviations identified during the inspections including generating detailed reports, maintaining inspection records, and communicating findings to area supervisor or manager. Effective documentation and reporting facilitate traceability, support corrective actions, and contribute to the overall quality assurance process.

Education:
High school diploma or equivalent required.

Experience:

Required: Minimum of 2 years of work experience in QA or QC or related field
Preferred: Experience in a cGMP environment or QA & QC

Knowledge, Skills, Abilities:

Knowledge of automatic inspection equipment: Possesses a solid understanding of the operation and uses automatic inspection equipment specific to pharmaceutical labeling manufacturing. Capable of setting up and calibrating equipment, interprets, and analyses inspection results, and troubleshoots any equipment-related issues. Familiarity with automatic inspection equipment and its capabilities is crucial for effective quality control.
Ability to follow pacing and maintain production flow: Possesses the ability to follow pacing and maintains the production flow including effectively managing their time, ensuring inspections are conducted in a timely manner, and keeping up with the production schedule. Maintains attention to detail to prevent any bottlenecks in the manufacturing process.
Problem tracking and troubleshooting skills: Possesses strong problem tracking and troubleshooting skills and the ability to identify and track issues or deviations during inspections. Investigates root causes, and propose appropriate corrective actions. Applies analytical thinking and problem-solving abilities to address quality-related problems promptly and effectively. Maintains quality standards, minimizes disruptions, and ensures smooth operations in pharmaceutical trial labeling manufacturing.

Physical Requirements / Work Environment