QC Inspector - 2nd Shift

Innovative Health • Scottsdale, AZ

1d

About The Position

Innovative Health is seeking a QC Inspector to join its Operations team. The role performs sampling, inspection, and testing of incoming materials; in-process and final inspection of reprocessed devices and their packaging; pre- and post-sterilization batch inspection; and review of Batch History Records (BHRs). The QC Inspector follows and enforces established procedures and policies to meet quality requirements in a regulated medical device company.

The regular second-shift schedule is Monday through Friday, 2:00 p.m. to 10:00 p.m., with the opportunity for weekend overtime. Training takes place on first shift, 6:00 a.m. to 2:30 p.m., for approximately two months.

Requirements

• High school diploma or equivalent.
• Good written and verbal English communication skills.
• Good arithmetic skills.
• High attention to detail, including completing tasks and cross-referencing information in several locations.
• Ability to multitask and prioritize in a fast-paced environment, with flexibility to manage numerous projects simultaneously.
• General proficiency in Microsoft Word and other applications, including Excel, PowerPoint, Adobe Acrobat, and Visio.
• Ability to understand instructions and information rapidly and apply them with little supervision; self-motivated and able to work as a self-starter.
• Strong verbal, written, organizational, time-management, and interpersonal skills.

Nice To Haves

• 1–2 years of Quality Inspection experience.
• Mechanical aptitude and working knowledge of measuring instruments.
• Experience with 21 CFR 820, Quality Systems Regulation, and ISO 13485.
• Experience using J.D. Edwards ERP software.

Responsibilities

• Inspect purchased components, reprocessed devices and packaging, sterilization records, and Batch History Records according to controlled procedures and predetermined acceptance criteria.
• Accurately document inspection and testing results.
• Participate in creating and revising inspection-function procedures.
• Ensure product and materials are appropriately labeled, stored, and handled throughout the manufacturing facility to prevent mix-ups.
• Maintain orderly quarantine areas and fulfill scrapping requests made by the Materials Review Board (MRB).
• Update material status in the ERP system after completing Quality activities.
• Ensure line clearance and material reconciliation activities are conducted according to company procedures.
• Assist with nonconforming product investigations, CAPAs, and customer complaints.
• Perform other reasonable duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED