Packing and Labeling Technician 3 - Third Shift

Thermo Fisher Scientific•Allentown, PA

1d•Onsite

About The Position

This position is located at our Allentown, PA site within the Clinical Trials Division. The facility supports global clinical supply chain services, including labeling, packaging, and distribution of investigational medicinal products in a cGMP-regulated environment. How Will You Make an Impact? The Technician III is responsible for executing advanced clinical labeling and packaging operations with minimal supervision, ensuring compliance with cGMP, SOPs, and regulatory requirements. This role supports high-quality, on-time delivery of clinical trial materials that directly impact patient safety and study success. A Day in the Life Set up, operate, and monitor labeling and packaging equipment while ensuring adherence to batch records, work instructions, and quality standards Perform and document line clearances, in-process checks, reconciliation activities, and batch record review to ensure compliance and inspection readiness Identify and troubleshoot process or equipment issues, escalate as needed, and contribute to continuous improvement initiatives and Right First Time execution

Requirements

High school diploma or equivalent required.
Minimum of 2 years of experience in manufacturing, operations, production, lab, or a related environment.
Solid understanding of cGMP requirements, GDP (Good Documentation Practices), and quality systems.
Ability to follow detailed instructions, execute batch records, and maintain accurate documentation with a high degree of accuracy.
Proficiency in operating and troubleshooting packaging/labeling equipment.
Strong organizational skills and ability to manage multiple tasks in a fast-paced environment.
Effective communication skills and ability to work collaboratively within a team.
Basic computer proficiency (e.g., MS Office, electronic batch systems, ERP systems).
Ability to stand for extended periods and perform repetitive motions.
Ability to lift, push, and pull materials up to 40 lbs with or without accommodation.

Nice To Haves

Experience in a cGMP-regulated environment
Experience working in a cleanroom environment
Experience with labeling and/or packaging operations in a pharmaceutical or clinical supply setting

Responsibilities

Execute advanced clinical labeling and packaging operations with minimal supervision.
Ensure compliance with cGMP, SOPs, and regulatory requirements.
Support high-quality, on-time delivery of clinical trial materials.
Set up, operate, and monitor labeling and packaging equipment.
Ensure adherence to batch records, work instructions, and quality standards.
Perform and document line clearances, in-process checks, reconciliation activities, and batch record review.
Identify and troubleshoot process or equipment issues.
Escalate issues as needed.
Contribute to continuous improvement initiatives and Right First Time execution.