Quality Assurance Specialist

1 week ago

Orchard Park, New York, United States Viant, Inc. Full time
Job Summary

Viant, Inc. is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring the highest quality standards are met in our manufacturing process.

Key Responsibilities
  • Assist with first piece, in-process, and final inspection or test on a select group of parts and document results.
  • Indicate inspection status, maintain product traceability, and non-conforming material control.
  • Participate in internal audits, statistical process control, and assist control of process documentation, records, and equipment calibration.
Essential Duties and Responsibilities
  • Assist with required inspections, measurements, and testing of incoming parts, production first piece, in-process, and finished product per established criteria.
  • Record results on appropriate documentation. Communicate any discrepancies to the person(s) responsible for corrective/preventive action activity.
  • Assist with various dimensional inspections using specific dies, gages, microscopes, micrometers, and other dimensional inspection systems.
  • Indicate inspection status of parts with assigned labels and stamps.
  • Maintain product identification and traceability.
  • Control non-conforming product in accordance with documented procedures and verify timely corrective and preventative action.
  • Protect product during handling and storage in the performance of work.
  • Monitor factory environmental conditions, record data, and identify adverse conditions.
  • Assist with distribution and control of process documentation and quality records.
  • Assist with control of measuring and test equipment calibration.
  • Participate in internal quality audits to verify compliance with documented procedures and specifications, record results, and verify audit corrective action.
  • Assist with statistical methods of verifying and controlling process capability.
  • Provide information to production personnel on quality issues.
  • Comply with and reinforce the requirements of the Quality Manual and Standard Operating Procedures, ISO 13485, FDA Quality System Regulations, and other customer standards.
  • Follow Occupational Safety and Health regulations, including laser safety practices. Performs job duties with little or no supervision or assistance.
Environmental Working Conditions

Employee must comply with all safety policies and safe work procedures established by the company. Job tasks may also involve:

  • Using personal protective equipment such as safety glasses, goggles, gloves, and other equipment as established in company policies and safe work procedures.
  • Working near cutting & machining fluids, solvents, lubricants, and other hazardous chemicals using appropriate safety controls.
  • Lifting up to 50 pounds.
  • Frequent carrying, bending, standing, sitting, and repetitive motion.
Qualifications
  • Minimum 2 years' experience as an assembler or machine operator in a manufacturing or production environment with some inspection responsibilities required.
  • Prior medical device, aerospace, automotive, or regulated manufacturing environment preferred.
  • Progress towards certificate(s) of training related to this field of work (medical device industry or quality assurance) preferred.
  • Prior experience interpreting technical drawings & specifications required.
  • Proficiency in the use of measuring and test equipment preferred.
  • Demonstrate ability to check dimensions, surface relationships, finish material defects, and mechanical strength of product following appropriate training required.

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