Quality Inspector
Job in
Morrisville, Wake County, North Carolina, 27560, USA
Listed on 2026-08-01
Listing for:
SunTech Medical, Inc.
Full Time
position Listed on 2026-08-01
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Production QC/QA
Job Description & How to Apply Below
Summary The primary duties and responsibilities of the Quality Inspector are to help ensure the function, accuracy, and usability of components and parts by performing inspection activities according to documented processes and inspection plans.
Duties and Responsibilities The Inspector will be expected to work closely with members of the Quality team to:
Perform required inspection of incoming materials per standard operating procedures,Perform in-process inspections per standard operating procedures,Perform shipping audits per standard operating procedures,Be the primary communicator with other departments to resolve issues or gaps in inspection criteria or instructions,Generate Nonconformance reports to record and control failures from inspection activities.
Perform other inspections, audits, and duties as needed
Complete DHR audits to ensure released products are built according to released specifications
Complete verification checks for product and documentation from Nonconforming rework
Provide feedback to improve inspection plans based upon gaps identified
Quality Focus/Continuous Improvement Must maintain a quality first mindset and be process oriented.
Verbal and written communication must be appropriate for an audit.
Update and refine processes, procedures, and forms, practicing lean principles and implementing 6S.Identify improvement opportunities and participate in Kaizen events.
Active participant in QMS activities including complaint investigation, CAPA and regulatory compliance.
Must be detail oriented.
Qualifications,
Education and Experience An AA degree in a technical field or 1-3 years’ experience in inspection/quality related work in the medical device or other regulated field1-5 years’ experience in a manufacturing environment
Able to understand and follow component specifications, purchase and assembly drawings, test procedures, sampling plans and written instructions
Naturally curious and with strong ability to identify and resolve problems
Above average written and oral communication
Able to effectively and independently prioritize assignments & manage workload
Experience with Microsoft Office Suite
Experience with a medical device company is a plus
Physical Requirements:
Ability to visually inspect work and documentation with precision.
Stand for up to eight - ten hours per day, with the ability to move about, bend, stoop, use hands, and lift up to 35 pounds unassisted.
Possess fine motor skills for tasks requiring precision, such as assembling and handling small components.
If you are passionate about making a positive impact on people's lives, come grow with us!
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