Packaging Equipment Operator | 401k + PTO + Benefits

Aveva Drug Delivery Systems; Town of Florida (NY); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Medical/Dental/Vision Insurance

401k with employer match

Paid Time Off

Paid Holidays

Job summary

Aveva Drug Delivery Systems is seeking a set-up mechanic to operate and troubleshoot packaging equipment, perform line set-ups and minor repairs in a regulatory-driven manufacturing environment. You will work under general supervision to support production schedules.

Typically 1–3 years of relevant experience in manufacturing, with a focus on cGMP practices, safety, and quality documentation. This role emphasizes teamwork, reliability, and adherence to procedures in a fast-paced facility.

Qualifications

• High school diploma or equivalent, with hands-on or vocational training preferred.
• 1–3 years of experience as a set-up mechanic in a manufacturing environment.
• Familiarity with cGMP, FDA and other regulatory requirements.
• Reading, writing and speaking English; able to follow written and oral instructions.

Responsibilities

• Operate packaging equipment per procedures and packaging schedule.
• Perform routine troubleshooting and minor repairs of packaging/processing equipment.
• Set up and change over packaging lines; monitor line performance and document batch records.
• Escalate downtime issues to leadership and coordinate with Engineering Technician as needed.
• Maintain clean, safe, and compliant work areas; adhere to safety rules and company policies.

Skills

Mechanical aptitude

Basic mathematics

Troubleshooting

Reading & writing English

Communication

Team collaboration

Education

High school diploma or equivalent

Tools

Packaging equipment

Die cutting/punching tooling

Job description

Aveva Drug Delivery Systems is seeking a set-up mechanic to operate and troubleshoot packaging equipment, perform line set-ups and minor repairs in a regulatory-driven manufacturing environment. You will work under general supervision to support production schedules.

Typically 1–3 years of relevant experience in manufacturing, with a focus on cGMP practices, safety, and quality documentation. This role emphasizes teamwork, reliability, and adherence to procedures in a fast-paced facility.