QA Technician I – 2nd Shift Quality Expert

Perrigouk; Allegan Township (MI); On-site; USD 28,000 - 41,000; Full time

Job summary

Perrigo in Allegan Township, MI is seeking a QA Technician to respond to quality events, document actions, and determine immediate containment in a fast-paced, FDA-regulated setting.

You will review documentation, identify defects, and manage the rework process while auditing manufacturing and packaging for cGMP compliance. A high school diploma is required, with preference for advanced education; strong communication and analytical skills are essential.

Qualifications

• High school diploma or GED is required, with preference given to those with advanced education (2-year or 4-year degree, or progress toward a degree).
• A minimum of 2 years experience working in an FDA regulated industry is preferred; at least 6 months of experience is required.
• Must possess an understanding of and ability to apply cGMPs.
• Must have a working knowledge of SOPs and be able to provide clear direction and interpretation.
• Strong analytical skills are required.
• Excellent oral and written communication skills are essential, as are strong interpersonal skills.
• The ability to work independently against multiple deadlines is required.
• Must be able to understand equipment operation and manufacturing/packaging processes.

Responsibilities

• The QA Technician responds to quality events, completes related documentation, and determines immediate physical containment and remediation.
• They assist in identifying, assessing, and containing defects, and conducts ASP’s and manages the rework process including providing rework instructions.
• The QA Tech also reviews documentation as necessary and performs auditing of Perrigo manufacturing and packaging process to ensure that processes are in compliance with applicable cGMP requirements.

Job description

Perrigo in Allegan Township, MI is seeking a QA Technician to respond to quality events, document actions, and determine immediate containment in a fast-paced, FDA-regulated setting.

You will review documentation, identify defects, and manage the rework process while auditing manufacturing and packaging for cGMP compliance. A high school diploma is required, with preference for advanced education; strong communication and analytical skills are essential.