Pay: $25.00/hr, paid weekly
Schedule: Mon–Thurs (7 AM–4 PM), Fri (7 AM–11 AM)
Location: Madison, WI 53718
Duration: 6 months
SummarySupport daily manufacturing, processing, and packaging of medical devices to ensure compliance with GMP, FDA regulations, and company quality standards.
Key Responsibilities- Perform one of the following quality functions:
• Inspect raw materials.
• Conduct in-process inspections.
• Review final documentation and packaging. - Assist with document control in the Madison facility.
- Complete documentation and labeling; ensure secure product storage and handling.
- Support investigations of nonconformance and assist with preventive actions.
- Review quarantined items for internal release.
Qualifications- High School diploma or GED.
- 1+ year experience in a regulated environment preferred.
- Familiarity with FDA QSR and ISO 13485 standards.
Skills & Competencies- Self-motivated, detail-oriented, and independent
- Comfortable using computer-based systems
- Strong teamwork and communication skills
Benefits (employee contribution):
- Health insurance
- Health savings account
- Dental insurance
- Vision insurance
- Flexible spending accounts
- Life insurance
- Retirement plan
All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.