On-Site Manufacturing Engineer ​/ Quality Specialist

Vacancy Name

On‑Site Manufacturing Engineer / Quality Specialist

VN849

Full‑Time

Country:
United States
State:
New Jersey
City:
South Plainfield

The Manufacturing Engineer / Quality Specialist will play a key role in implementing process improvements within an efficient ISO‑9001:2015 compliant environment. The Mechanical Engineer / Quality Specialist will report directly to the Plant Manager with a dotted line reporting to the company president. An elevated level of independent activity is expected. This position is on‑site.

• Support manufacturing processes, including failure analysis, documentation review and approval, equipment qualification/calibration, and defect containment.
• Ensure manufacturing activities follow QMS.
• Support development and execution of process validation and verification test plans, protocols, and reports.
• Perform and coordinate PPAP inspections and product verification activities.
• Ensure compliance with drawings, specifications, and customer requirements.
• Administer and improve quality processes, with a focus on Lean process management.
• Assist manufacturing and product development with documentation, guidance, and execution of design verification/validation and process validation.
• Lead implementation and improvement of manufacturing‑related quality processes.

• Lead and manage initiatives in multiple product and process quality areas.
• Ensure successful, on‑time completion of continuous improvement and capex projects.
• Support internal and external audits, prepare and review back‑room documentation.
• Full responsibility of change order and deviation processes.
• Lead timely investigation (root cause analysis), disposition (including corrective and preventative actions), tracking, and reporting of non‑conformances (NCP), both internal and supplier related.
• Track KPIs including delivery performance, NCPs, cost of quality, and customer satisfaction.
• Ensure QMS integrity during changes and process improvements.
• Maintain technical documentation in support of QMS.

• Maintain and improve the ISO 9001:2015 Quality Management System.
• Control and update the Quality Manual, procedures, and work instructions.
• Maintain and administer IQM (Ideagen Quality Management) system including document control, audits, assets, and workflow processes.
• Perform, coordinate and support internal and external (including customer) audits.
• Identify risks and opportunities and support QMS planning and improvements.
• Ensure controlled implementation of QMS changes and improvements in compliance with ISO standards.

The employee may be required to perform other non‑essential functions, follow any other job‑related instructions, and perform any other job‑related duties requested by their supervisor.

Education:

associate’s degree in industrial engineering (IE), manufacturing engineering technology (MET), or equivalent (bachelor’s degree preferred).

Skills:

Pragmatic, entrepreneurial personality, and strong initiative‑taker. Continually strives to improve.

Experience:

A minimum of 3‑5 years of working experience in a manufacturing engineering capacity.

• Health/Prescription Coverage
• FSA or HSA
• Dental
• Vision
• Life Insurance
• Company‑match 401(k) Plan
• Vacation/Sick/Paid Holidays
• All benefits start on date of hire

Physical requirements section is currently not detailed.