Quality Operations Technician (Weekend 12 Hour Night Shift - Onsite)
About The Position
Join a fast-growing, innovation-driven organization as an Operations Quality Technician I, where you’ll play a key role in ensuring high-quality medical device manufacturing. In this hands-on role, you’ll perform inspections across incoming materials, in-process production, and final product release to ensure compliance with rigorous quality and regulatory standards. You’ll work in a cleanroom environment, utilize advanced measurement tools, and contribute to continuous improvement in a dynamic, fast-paced setting. This is an excellent opportunity for detail-oriented professionals who thrive in quality-driven environments and want to grow their careers while supporting cutting-edge manufacturing and product innovation. This is a weekend night shift position. Working hours are 6:00 pm - 6:30 am, Friday - Sunday. This position is eligible for additional shift differential pay. The Operations Quality Technician will be a critical contributor in a mission that truly represents a once-in-a-lifetime opportunity to join a company that is making significant investments in establishing US manufacturing, expanding internationally, and delivering a consistent cadence of product innovations to the market and investing in its people. The successful candidate will be responsible for ensuring our manufacturing site produces and distributes products which meet or exceed all established quality standards and will be responsible for ensuring our processes and procedures are compliant with corporate policies and federal law. The individual will be trained in performing Incoming, In-process inspections in the cleanroom, or assessing the final product’s efficacy prior to market release. In addition to those activities, this position may also be required to support production operations, metrology, microbiology, or other manufacturing functions as business needs arise. This position requires a strong attention to detail, problem solving skills, and willingness to work in a fast-paced manufacturing environment.
Requirements
- High School diploma
- 1 year of experience in manufacturing or a highly regulated environment.
- Excels at the organization and maintenance records accurately.
- Self-starter capable of dealing with a variety of tasks in a fast paced, multi-tasking environment.
- Must be proficient in English language to be able to read documentation, communicate, and write.
- Mathematics – Basic mathematics skills (adding, subtracting, multiplying, dividing)
- Autonomy - Capable of working independently with minimal instruction from their supervisor.
Nice To Haves
- Familiarity with measurement instrumentation such as micrometers, calipers, tensile testers, video microscopes, and optical gauging products preferred, not required.
- Experience working in a lab setting environment in the medical device industry preferred but not required.
- The ability to use stereoscopes and varying microscope setups preferred but not required.
Responsibilities
- Inspect and record results of work on Incoming raw material, In-process, or Lot Qualification at various stages of the production process, distribution process to determine and maintain the quality and reliability of our product.
- Assess and complete inspection reports and records including the entry of data into various electronic systems. (For example – Word, Excel, SAP, Electronic DHR systems, Oracle Agile, and others).
- Generate, review, and maintain quality records in support of the Quality System. (For example – device history records and training records)
- Ensure the equipment calibration status is within the timeframe of use.
- Assist the Quality Manager in notified body and regulatory authority audits and inspections.
- Works from specifications, work plans, procedures, and general instructions from either Quality Engineers, Quality Supervisor, or the Quality Manager.
- Required to maintain and enforce cGMPs.
- Safely follow standard operating procedures including but not limited to quality standards, material handling, and record keeping. Must follow all Good Manufacturing Practices (GMPs), Good Documentation Practices (GDPs), and Good Laboratory Practices (GLPs).
- Notifies Quality or Operations Leadership of any discrepancies to ensure quality standards and safety of operations are maintained at all times.
- Maintain a clean work environment suitable for medical device manufacturing and cleanroom production.
- Performs other duties as required
Benefits
- Medical, dental, and vision insurance
- 401(k) with company match
- Paid time off (PTO)
- Additional employee wellness programs
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
