Spellman High Voltage Electronics Corporation, a family owned business for over 75 years, takes pride in powering progress in health, security and quality of life. We are key partners with the world's leading medical devices, semiconductor, scientific analytics and industrial systems manufacturers. When they want to push the limits of what's possible with high voltage applications, they turn to us to make it happen.
While Spellman is not a household name, our products are used to make and often power many of the most advanced technologies that make modern life possible. With design and manufacturing sites in North America, Europe and Asia, we have become the preferred provider of high voltage power solutions for OEMs pushing the boundaries of technology around the world by designing and producing the products they need to power progress.
What You Will Do
- Lead Material Review Board (MRB) activities - r eviewing , dispositioning , and resolving defects and nonconforming conditions in complex electrical, mechanical , and optical assemblies.
- Establish turnaround times, c oordinate meetings, and lead initiatives to ensure timely disposition of MRB materials. Escalate as required.
- Ensures compliance with existing MRB/Quality procedures and/or process control documentation, and train team members as necessary .
- Assist the QA/QC Engineer in conducting Good Practice Trainings, In-process Inspections, identifying defective works, conducting in-house testing, in-house Quality Assessment
- Lead a team of QA/QC Technicians and QC Inspector.
- Maintain and control QA/QC practices with regular checks and inspections ensuring correct operation and implementation of procedures.
- Able to follow material specification as instructed by QA/QC Engineers
- Assist in the development and monitoring of key quality goals & objectives for services and processes
- Ensure good performance by quality assurance technicians/auditors/Inspectors by mentoring, training, setting expectations, providing accountability, and performing evaluations.
- Assist in defining Quality Key Performance Indicators (KPIs), develop action plans and execute
- Monitor quality data to identify trends, recognize correlations in issues, and proactively initiate appropriate actions
- Ensure customer satisfaction by chairing customer phone calls, meetings, site visits, etc.
- Implement "Best Practices" into site location
- Able to conduct and drive failure analysis of defects through root cause and lab analysis
- Monitor and control Cost of Poor Quality (COPQ) through improved engineering practices via process engineering, product design & development, quality engineering, supplier quality, and all other aspects of the product development to customer application process.
- Assist in the implementation of policies, operating procedures, quality systems and programs which ensure proper testing, evaluation, inspection, and technical support in order to meet product quality standards.
- Participate in all regulatory, third party and customer audits and inspections, and corrective action response.
What You Need
- BS/ MS in Electrical Engineering or an Engineering degree with electronics assembly experience
- 2 years of experience as a Quality Professional
- ISO 9001 experience required; FDA regulatory experience and/or ISO13485 experience a plus
- Proficient in English comprehension and expression; including reading and writing
- Experience with MRP systems i.e. Glovia
- Knowledge of Lean concepts preferred - 5S, Kanban, VSM's
- Well-developed computer skills
- Able to use MS Office products
- Ability to work independently and exercise sound judgment and discretion
- Excellent Project Management Skills
- Outstanding interpersonal and communications skills
- Strong organizational and time management skills
- It will be a working supervisor role
Our good faith estimate of the salary range for this role is $72,000 - $100,000. Exact compensation may vary based on skills, experience, and other factors. In addition to base pay, we offer a full benefits package.
Spellman Takes Safety Seriously
All new hires are required to provide proof of COVID vaccination at start, or must request and be granted a religious or medical exemption.
This position requires on-site presence at Spellman High Voltage headquarters in Hauppauge, NY .
#LI-Onsite
WORKING CONDITIONS
Working conditions are normal for an office environment. Must be able to sit and work at a computer keyboard for extended periods; able to stoop, kneel, bend at the waist and reach on a daily basis; able to perform general office administrative activities: copying, filing, delivering and using the telephone.
We at Spellman High Voltage Electronics Corporation believe that each individual is entitled to equal employment opportunities without regard to race, color, creed, gender, sexual orientation, gender identity, marital status, national origin, age, veteran status or disability. The right of equal employment opportunity extends to recruiting, hiring selection, transfer, promotion, training and all other conditions of employment. To request accommodation related to disabilities, please email us at careers@spellmanhv.com, or call +1 (631) 630-3000
Note to Recruiters and Placement Agencies: Spellman High Voltage Electronics does not accept unsolicited agency resumes. Please do not forward unsolicited agency resumes to our website or to any Spellman High Voltage Electronics employee. Spellman High Voltage Electronics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Spellman High Voltage Electronics and will be processed accordingly.