Quality Control Technician

Nissha•Sandpoint, ID

9d•$20 - $22•Onsite

About The Position

Nissha Medical Technologies (NMT) is a global Contract Development and Manufacturing Organization (CDMO) where people, purpose, and technology come together to advance healthcare. Headquartered in the United States, NMT is the medical devices business unit and a wholly owned subsidiary of Nissha Co., Ltd., a publicly traded Japanese company based in Kyoto, Japan (TSE: 7915). Across our global organization, our teams collaborate to design and manufacture innovative medical devices and solutions that make a real difference in patients’ lives. We partner closely with our customers to solve complex challenges, move ideas forward, and support products from concept through commercialization. Our work spans patient monitoring, surgical and interventional solutions, precision components, and emerging technologies, all grounded in a strong culture of quality, accountability, and continuous improvement. At Nissha Medical Technologies, we believe our success is driven by our people. We foster an environment where curiosity is encouraged, teamwork is valued, and individuals are empowered to grow their skills and careers. If you’re motivated by meaningful work, collaboration, and the opportunity to help shape the future of healthcare, you’ll find a place to belong at NMT.

Requirements

Demonstrated understanding of cGMP and the importance of adherence to government and ISO requirements
Must have strong organizational, communication, and analytical skills
Ability to take accurate measurements and record data accurately
Comfortable and skilled at operating tools and equipment
Ability to maintain accuracy while under time constraints
Excellent interpersonal skills with ability to interact effectively with all employees in all departments
Strong written and verbal communication skills required
Detail oriented with attention to accuracy
Analytical skills with ability to understand problems and present effective recommendations for resolution
Ability to resolve problems by gathering necessary information in order to make an effective resolution
Organized with ability to multi-task and prioritize
Flexibility to adapt to frequent changes

Nice To Haves

High School diploma preferred
One year in a production environment preferred
Previous Quality Control experience desired
Proficiency in Microsoft Office Suite required with strong MS Excel experience desired

Responsibilities

Perform Incoming Inspections: take measurements, perform tests & record data.
Work closely with Production Department to understand manufacturing priorities.
Implement and ensure execution of all inspection activities.
Perform document reviews using current GDP.
Draft Non-Conformances and CAPA.
Perform tests and inspections on product as required and document results.
Responsible for assessing the quality of manufactured parts by conducting in-process inspections.
Perform First Part Checks, In-Process Inspections, Final Release, and ensure adherence to cGMP, FDA 21 CFR 820 and ISO 13485 standards.
Maintain cleanliness of QC Lab/Testing area.
Perform cleanliness inspection.
Conduct quality-related training in a timely manner.
Ensures company policies and procedures are followed to ensure conformance and consistency of products. Remains current on all company policies and procedures.
Abide by all safety and security rules set forth by the company and regulatory agencies.
Regular attendance is required.
Other duties as assigned.