Packaging / Labeling Tech 3 - 2nd & 3rd Shifts

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.

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.

Education:

High School Diploma OR GED Required

Experience:

Required: Minimum of 2 years of work experience in a manufacturing, operations, production, lab setting, or related field
Preferred: Experience in a cGMP environment
Preferred: Experience working in a clean room environment

Knowledge, Skills, Abilities:

• 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.

Physical Requirements / Work Environment:

• 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.

What We Offer:

Compensation

Competitive Pay
Performance Related Bonus where eligible
Annual merit performance-based increase

Excellent Benefits

Medical benefits
Paid Time Off / Annual Leave
Employee Referral Bonus
Career Advancement Opportunities