Evening QA Technician I - cGMP & Manufacturing

Perrigo Company plc; Michigan; On-site; USD 30,000 - 39,000; Full time

Benefits offered by this job

Total Rewards

Forbes recognition

Job summary

Perrigo Company plc is seeking a QA Technician for a 2nd shift (Mon-Fri, 3 PM–11 PM) to respond to quality events and ensure compliant manufacturing and packaging processes in Michigan. You will help contain defects, guide rework, and review documentation for cGMP compliance.

The ideal candidate has FDA-regulated industry experience, strong analytical and communication skills, and the ability to work independently under deadlines.

Qualifications

• Minimum 2 years in an FDA-regulated industry; at least 6 months required.
• Must understand and apply cGMPs.
• Working knowledge of SOPs with ability to interpret.
• Strong analytical skills and attention to detail.
• Excellent oral and written communication and interpersonal skills.
• Ability to meet multiple deadlines while working independently.
• Ability to understand equipment operation and manufacturing/packaging processes.

Responsibilities

• QA Technician responds to quality events, determines containment and remediation.
• Assist in identifying, assessing, and containing defects; provide rework instructions.
• Review documentation and audit Perrigo manufacturing/packaging for cGMP compliance.

Skills

Analytical skills

Oral and written communication

cGMPs knowledge

SOPs knowledge

Independent work under deadlines

Equipment operation understanding

Interpersonal skills

Education

High school diploma or GED

Job description

Perrigo Company plc is seeking a QA Technician for a 2nd shift (Mon-Fri, 3 PM–11 PM) to respond to quality events and ensure compliant manufacturing and packaging processes in Michigan. You will help contain defects, guide rework, and review documentation for cGMP compliance.

The ideal candidate has FDA-regulated industry experience, strong analytical and communication skills, and the ability to work independently under deadlines.