Pharma Packaging Technician - 2nd Shift

ALMAC Group; Lower Providence Township (PA); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

Medical, Vision & Dental

PTO 20 days + 12 holidays

Disability & Life Insurance

401(k) match

Professional development

Job summary

Almac Group is seeking a 2nd Shift Production Operator at our Audubon, PA location to perform packaging duties ensuring product quality for patient safety. Responsibilities include equipment setup and operation, documentation, and communication of issues within contained processing environments.

The role requires at least a high school diploma or GED with 1+ year machine/mechanical experience and 2+ years in operations, preferably in a pharmaceutical/GMP setting.

Qualifications

• High School Diploma or GED.
• Minimum one year Machine/Mechanical or related experience.
• Minimum two years Operations or related experience.
• Experience with Processing or mechanical equipment in a GMP environment.

Responsibilities

• Set up, operate, shut down, and clean all production equipment in a cgMP environment per SOPs.
• Complete all required documentation per SOPs with accurate information.
• Perform roll changes, clear jams, and minor troubleshooting on equipment.
• Ensure only validated equipment is used for production operations.
• Maintain log books per SOPs and ensure setup matches batch documentation.
• Communicate machine inefficiencies to Production Mechanic and work in contained processing operations.

Skills

Machine/Mechanical experience

Operations experience

Education

High School Diploma or GED

Job description

Almac Group is seeking a 2nd Shift Production Operator at our Audubon, PA location to perform packaging duties ensuring product quality for patient safety. Responsibilities include equipment setup and operation, documentation, and communication of issues within contained processing environments.

The role requires at least a high school diploma or GED with 1+ year machine/mechanical experience and 2+ years in operations, preferably in a pharmaceutical/GMP setting.