2nd Shift QA Technician – cGMP & Quality Assurance

Biopharma Careers; Michigan; On-site; USD 40,000 - 60,000; Full time

Job summary

Perrigo is seeking a QA Technician for 2nd shift to respond to quality events, document actions, and implement immediate containment and remediation. You will assist in identifying defects and manage rework instructions while adhering to cGMP requirements.

The role emphasizes strong analytical and communication skills, the ability to work independently against multiple deadlines, and familiarity with SOPs and manufacturing processes.

Qualifications

• High school diploma or GED required; advanced education preferred.
• Minimum 2 years in an FDA-regulated industry; at least 6 months preferred.
• Must understand and apply cGMPs.
• Working knowledge of SOPs; ability to give clear direction and interpretation.
• Strong analytical and communication skills are essential.
• Ability to work independently against multiple deadlines.
• Must understand equipment operation and manufacturing/packaging processes.

Responsibilities

• Respond to quality events and complete related documentation.
• Determine immediate containment and remediation actions.
• Identify, assess, and contain defects; provide rework instructions.
• Review documentation and audit Perrigo manufacturing/packaging for cGMP compliance.
• Support rework processes and ensure compliance with SOPs.

Skills

Analytical skills

Communication skills

Independent work

cGMP knowledge

SOPs familiarity

Equipment operation understanding

Education

High school diploma or GED

2-year or 4-year degree in progress

Pursuing higher education encouraged

Job description

Perrigo is seeking a QA Technician for 2nd shift to respond to quality events, document actions, and implement immediate containment and remediation. You will assist in identifying defects and manage rework instructions while adhering to cGMP requirements.

The role emphasizes strong analytical and communication skills, the ability to work independently against multiple deadlines, and familiarity with SOPs and manufacturing processes.