Quality Technician III

Ultralife Corporation; Village of Newark (NY); Vor Ort; USD 39.000 - 45.000; Vollzeit

Zusammenfassung

Ultralife Corporation in Newark, NY is seeking a Quality Technician III for on-site work. The role focuses on advanced inspection, testing, data analysis, and problem solving to maintain and improve product quality.

Candidates should have strong documentation, SPC usage, and cross-functional collaboration skills. Preferred candidates hold a Technical Diploma with 10+ years of relevant experience, solid GD&T knowledge, and exposure to CAPA/8D methods.

Qualifikationen

• At least 10+ years of relevant work experience is required.
• Excellent written, oral communication, organization and computer skills required.
• Quality-oriented mindset, adaptability, collaborative, service-oriented traits are required.
• Training related to lead auditor and ISO training class for ISO 13485 and 9001 preferred.
• NCMR, CAPA / 8D experience.
• Root Cause Problem Solving.
• Understands GD&T principles.
• CMM, Keyence Programming experience preferred.

Aufgaben

• Perform advanced inspections, measurements, and testing of incoming materials, in-process components, and finished products to verify compliance with drawings, specifications, procedures, and established quality requirements.
• Interpret engineering drawings, specifications, work instructions, inspection criteria, and other technical documentation to determine product acceptance.
• Identify, document, categorize, and communicate nonconforming material and product conditions; initiate or support nonconformance documentation and disposition activities in accordance with established procedures.
• Collect, analyze, and trend quality data to identify recurring defects, process variation, and opportunities for improvement.
• Apply statistical process control (SPC) techniques and other basic statistical methods to monitor process performance, identify trends, and support evaluation of process stability and capability.
• Support root-cause investigations, corrective and preventive actions (CAPA), and continuous improvement activities using structured problem-solving tools such as 5-Why, Fishbone, and other applicable methodologies.
• Perform or support product rework, verification, and reinspection activities in accordance with approved procedures and instructions.
• Collaborate with Quality, Engineering, Manufacturing, Supply Chain, and other cross-functional teams to investigate and resolve product and process quality issues.
• Support supplier quality activities, including inspection of supplier material, documentation of supplier-related nonconformances, and collection of objective evidence needed for supplier corrective actions.
• Support internal, customer, supplier, and regulatory audits by providing records, inspection documentation, and other objective evidence as requested.
• Create, update, and maintain quality records and inspection-related documentation, including inspection instructions, checklists, data collection records, defect reports, and quality reports.
• Support First Article Inspection (FAI), new product introduction (NPI), process qualification, and validation activities by performing inspections, measurements, testing, and documentation as required.
• Verify the proper use and condition of inspection and measurement equipment and ensure equipment used for product acceptance is within its required calibration status.
• Provide technical guidance, training, and mentoring to Quality Technicians, Inspectors, and production personnel regarding inspection methods, workmanship requirements, defect identification, and quality procedures.
• Participate in Material Review Board (MRB) and other quality review activities by providing inspection results, defect information, measurement data, and technical input as required.
• Identify and communicate opportunities to improve inspection methods, product quality, process controls, efficiency, and defect prevention.
• Maintain accurate and complete quality records in accordance with company procedures, applicable regulatory requirements, and the Quality Management System.
• Follow all applicable safety, quality, regulatory, and company policies and procedures and perform other quality-related duties as assigned.

Kenntnisse

Advanced inspection

Data analysis

Problem solving

Statistical process control

Communication

GD&T understanding

CMM programming

Keyence programming

Ausbildung

Technical Diploma

Tools

CMM

Keyence programming

Jobbeschreibung

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Technician III

UL 17100 - Newark Quality Old 11710 Full-time Regular Technical Newark, NY, US

2 days ago Requisition ID: 1520

Salary Range: $28.00 To $33.00 Hourly

This position is on-site in Newark, NY.

Job Summary:

The Quality Technician III is responsible for supporting and improving product and process quality through advanced inspection, testing, rework, data analysis, and problem-solving activities. This role supports the identification and resolution of quality issues, participates in continuous improvement initiatives, and collaborates with cross-functional teams to ensure products and processes meet established quality requirements and applicable standards.

Essential Functions*:

• Perform advanced inspections, measurements, and testing of incoming materials, in-process components, and finished products to verify compliance with drawings, specifications, procedures, and established quality requirements.
• Interpret engineering drawings, specifications, work instructions, inspection criteria, and other technical documentation to determine product acceptance.
• Identify, document, categorize, and communicate nonconforming material and product conditions; initiate or support nonconformance documentation and disposition activities in accordance with established procedures.
• Collect, analyze, and trend quality data to identify recurring defects, process variation, and opportunities for improvement.
• Apply statistical process control (SPC) techniques and other basic statistical methods to monitor process performance, identify trends, and support evaluation of process stability and capability.
• Support root-cause investigations, corrective and preventive actions (CAPA), and continuous improvement activities using structured problem-solving tools such as 5-Why, Fishbone, and other applicable methodologies.
• Perform or support product rework, verification, and reinspection activities in accordance with approved procedures and instructions.
• Collaborate with Quality, Engineering, Manufacturing, Supply Chain, and other cross-functional teams to investigate and resolve product and process quality issues.
• Support supplier quality activities, including inspection of supplier material, documentation of supplier-related nonconformances, and collection of objective evidence needed for supplier corrective actions.
• Support internal, customer, supplier, and regulatory audits by providing records, inspection documentation, and other objective evidence as requested.
• Create, update, and maintain quality records and inspection-related documentation, including inspection instructions, checklists, data collection records, defect reports, and quality reports.
• Support First Article Inspection (FAI), new product introduction (NPI), process qualification, and validation activities by performing inspections, measurements, testing, and documentation as required.
• Verify the proper use and condition of inspection and measurement equipment and ensure equipment used for product acceptance is within its required calibration status.
• Provide technical guidance, training, and mentoring to Quality Technicians, Inspectors, and production personnel regarding inspection methods, workmanship requirements, defect identification, and quality procedures.
• Participate in Material Review Board (MRB) and other quality review activities by providing inspection results, defect information, measurement data, and technical input as required.
• Identify and communicate opportunities to improve inspection methods, product quality, process controls, efficiency, and defect prevention.
• Maintain accurate and complete quality records in accordance with company procedures, applicable regulatory requirements, and the Quality Management System.
• Follow all applicable safety, quality, regulatory, and company policies and procedures and perform other quality-related duties as assigned.

Education / Training / Skills / Experience:

• Technical Diploma preferred
• At least 10+ years of relevant work experience is required
• Excellent written, oral communication, organization and computer skills required
• Quality-oriented mindset, adaptability, collaborative, service-oriented are also some of the required traits
• Training related to lead auditor and ISO training class for ISO 13485 and 9001 preferred
• NCMR, CAPA / 8D experience
• Root Cause Problem Solving
• Understands GD&T principles
• CMM, Keyence Programming experience preferred

Physical Requirements:

General office, lab and production environments with occasional lifting of up to 30 lbs.

*Employees must be able to perform the essential functions of the job with or without reasonable accommodation.

This job description is intended to convey information essential to understanding the scope of the position described above and it is not intended to be an exhaustive list of skills, efforts, duties, responsibilities or working conditions associated with the position.

Ultralife Corporation is an Equal Opportunity Employer, and as such affirms the right of every person to participate in all aspects of employment without regard to race, color, religion, sexual orientation, gender identity, national origin, citizenship, sex, age, veteran status, disability, genetic information, or any other protected characteristic. If you are interested in applying for employment and need special assistance or an accommodation to apply for a posted position, contact our Human Resources department via phone at 315- 332-7100.

The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs.