2nd Shift Packaging & Visual Inspection Operator

Ferring Pharmaceuticals Inc.; Parsippany-Troy Hills (NJ); On-site; USD 43,000 - 55,000; Full time

Benefits offered by this job

Healthcare benefits

401(k) plan

Paid time off

Job summary

Ferring Pharmaceuticals Inc. in Parsippany, New Jersey, is seeking a Packaging & Visual Inspection Operator II for 2nd shift to ensure sterile product quality through packaging, labeling, and visual checks in a tightly regulated manufacturing environment.

You will follow approved procedures, document all activities, and collaborate with Operations and Quality teams to meet production goals, while maintaining data integrity and compliance with cGMP.

Qualifications

• High school diploma or equivalent required; degree preferred.
• Experience in pharmaceutical manufacturing or regulated environment preferred.
• Ability to read procedures and perform basic calculations.
• Basic computer skills and data entry.

Responsibilities

• Operate, monitor, clean, and change over packaging, labeling, and visual inspection equipment.
• Perform packaging and visual inspection activities following approved procedures and specifications.
• Identify defective or nonconforming products.
• Complete batch, inspection, equipment, and reconciliation records accurately.
• Follow SOPs, safety, gowning, data integrity, and quality requirements.
• Escalate quality concerns, defects, deviations, and equipment issues promptly.
• Maintain qualifications, training, and participate in continuous improvement.
• Work assigned shifts, overtime, weekends, or holidays when required.

Skills

Attention to detail

Teamwork

Basic math

Reading procedures

Written communication

Education

High school diploma or equivalent

Associate or bachelor's degree preferred

Job description

Ferring Pharmaceuticals Inc. in Parsippany, New Jersey, is seeking a Packaging & Visual Inspection Operator II for 2nd shift to ensure sterile product quality through packaging, labeling, and visual checks in a tightly regulated manufacturing environment.

You will follow approved procedures, document all activities, and collaborate with Operations and Quality teams to meet production goals, while maintaining data integrity and compliance with cGMP.