Commercial Tech 3 - Third Shift

Thermo Fisher Scientific•Allentown, PA

7d•Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: This position is located in Allentown, PA within the Pharma Services Group, Clinical Trials Division. Our team provides global commercial and clinical packaging and labeling services to pharmaceutical and biotech partners, ensuring patients receive the right therapies at the right time. How Will You Make an Impact?: You will ensure packaging operations are executed safely, accurately, and in compliance with cGMP standards. By supporting Engineering, Quality, and Production teams, you will help drive operational efficiency while maintaining the highest standards of quality and accountability. A Day in the Life: Support Engineering with equipment setup and configuration, especially during multiple or complex equipment changeovers. Support basic equipment troubleshooting Partner with the Room Leader to stage and verify components, initiate batches in the system, and confirm scan accuracy to ensure material traceability and compliance. Perform daily equipment challenges, quality shift inspections, AQL inspections, pallet inspections, accountability verifications, and assist with TOE log completion and verification.

Requirements

High school diploma or equivalent required.
Minimum of 2 years of work experience in a manufacturing, operations, production, lab setting, or related field
Strong attention to detail and ability to follow SOPs and batch documentation accurately.
Working mathematical skills including addition, subtraction, multiplication, division, fractions, and percentages.
Ability to interpret 2D diagrams and production documentation.
Strong communication skills and ability to work collaboratively with cross-functional teams (Engineering, QA, Room Leaders).
Basic computer proficiency for system batch entry and documentation tasks.
Ability to work in Primary, Secondary, Refrigerated (2–8°C), and Frozen (-20°C) environments.
Ability to stand and walk for extended periods (50–80% of shift).
Ability to lift and/or carry up to 50 pounds frequently.
Frequent bending, squatting, reaching, and repetitive hand movements requiring manual dexterity.
Ability to work in both hot and cold environments as required.
Must meet vision requirements including distance vision, color vision, depth perception, and ability to adjust focus.

Nice To Haves

Experience in a cGMP environment
Experience working in a clean room environment

Responsibilities

Support Engineering with equipment setup and settings to ensure proper equipment readiness and efficiency.
Stage and verify components alongside the Room Leader to support both legacy and updated documentation processes.
Start batches in the system in coordination with the Room Leader.
Verify material scans with the Room Leader to ensure traceability and accuracy.
Perform daily equipment challenges in partnership with Engineering.
Conduct quality shift inspections to ensure ongoing compliance with cGMP and internal quality standards.
Perform AQL (Acceptable Quality Level) inspections.
Pull samples in collaboration with QA for required testing and documentation.
Perform pallet inspections to ensure proper configuration and labeling.
Complete accountability verifications to ensure accurate reconciliation of materials.
Assist with production documentation log completion and verification, requiring strong mathematical skills and attention to detail.