Sr QC Technician

Thermo Fisher Scientific; North Great River (NY); On-site; USD 10,000 - 60,000; Full time

Job summary

A leading company is seeking a Sr QC Technician to ensure the quality and integrity of production processes. Responsibilities include monitoring inspections, documenting results, and maintaining safety standards. Join a collaborative environment with comprehensive benefits and opportunities for growth.

Benefits

Comprehensive benefits including medical, dental, vision

PTO

Tuition reimbursement

Qualifications

• Minimum 2 years experience in QA/QC or related field.
• Experience in a cGMP environment.

Responsibilities

• Operate and monitor automatic inspection equipment.
• Perform QC inspections, visually examining labels.
• Document inspection results and report non-conformities.

Skills

Problem Tracking

Troubleshooting

Teamwork

Education

High school diploma or equivalent

Job description

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Environmental Conditions

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

Work Schedule

Second Shift (Afternoons)

Location/Division Specific Information

Clinical Labeling Services, part of the Clinical Trials Division, located in Bohemia, NY, provides leading clinical label design, production, and management services for the pharmaceutical and biotechnology industry. Our advanced inspection software, full in-house print capabilities, and proprietary translation and regulatory approval system are designed to reduce overall clinical trial label cycle times.

Role Impact

The In Process Inspector ensures the quality and integrity of the production process by monitoring and inspecting manufacturing stages, using automatic equipment or visual inspection of labels. Their vigilance helps prevent defects, ensures product safety, and maintains process efficiency.

Typical Day

Shift Schedule: 2nd Shift 03:00pm - 11:30pm

• Operate and monitor automatic inspection equipment to assess label quality, set up, conduct routine checks, interpret results, and identify defects or change requests.
• Perform QC inspections, visually examining labels, verifying content, conducting counts, checking alignment, and assessing print quality to ensure standards are met.
• Document inspection results, report non-conformities, generate reports, and communicate findings to supervisors.

Qualifications

• High school diploma or equivalent
• Minimum of 2 years experience in QA/QC or related field
• Experience in a cGMP environment

Knowledge, Skills, and Abilities

• Understanding of automatic inspection equipment specific to pharmaceutical labeling
• Ability to follow pacing and maintain production flow
• Strong problem tracking and troubleshooting skills

Physical Requirements / Work Environment

• Fast-paced environment requiring teamwork

Compensation and Benefits

• Hourly pay rate: $25.00–$27.00
• Shift differential for second shift
• Performance-based bonuses and merit increases
• Comprehensive benefits including medical, dental, vision, PTO, holidays, retirement plans, tuition reimbursement, and more

Our mission is to enable our customers to make the world healthier, cleaner, and safer. Join us to make a positive impact globally and advance your career in a collaborative environment that values diversity and innovation.