Evening Packaging QA Technician – cGMP & Audits

Biopharma Careers; Michigan; On-site; USD 25,000 - 39,000; Full time

Job summary

Perrigo is seeking a QA Technician for a 2nd shift (3 PM–11 PM). The role focuses on responding to quality events, containment, and remediation, with responsibilities including process auditing to ensure cGMP compliance and overseeing rework instructions.

The ideal candidate has a high school diploma or GED, 2+ years in an FDA-regulated environment, and strong analytical and communication skills. The position emphasizes independent work and adherence to SOPs.

Qualifications

• High school diploma or GED required; advanced education preferred.
• Minimum 2 years in an FDA-regulated industry preferred; at least 6 months required.
• Understanding and application of cGMPs.

Responsibilities

• Respond to quality events and determine immediate containment and remediation.
• Review documentation and audit Perrigo manufacturing and packaging processes for cGMP compliance.
• Manage rework process and provide rework instructions.

Skills

Quality assurance

cGMP

SOPs

Analytical skills

Communication

Education

High school diploma or GED

Progress toward degree

Tools

Equipment operation

Job description

Perrigo is seeking a QA Technician for a 2nd shift (3 PM–11 PM). The role focuses on responding to quality events, containment, and remediation, with responsibilities including process auditing to ensure cGMP compliance and overseeing rework instructions.

The ideal candidate has a high school diploma or GED, 2+ years in an FDA-regulated environment, and strong analytical and communication skills. The position emphasizes independent work and adherence to SOPs.