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Senior Quality Engineer

  • LocationSomerset, NJ 08873 - United States
  • Work TypeFull time
  • Positions1 Position
  • Published At:3 days ago
  • Job no: 39996
  • Category: Maintenance/Engineering

Job Description


A brilliant opportunity exists for an outstanding individual capable of fitting into this very rewarding Senior Quality Engineer role. Our client, a leading medical device company, is looking to hire someone who can bring added value to the team. If you’re dedicated, energetic and detail-oriented, this could be the perfect role for you. Responsibilities include:


1) Collect production data and apply standard scientific and statistical methods to analyze, document and diagram production processes

2) Conduct FMEA, DOE and SPC analysis

3) Perform complex data analysis and use six sigma tools to resolve complex quality issues

4) Provide input to the production control systems and design control activities

5) Provide input for new product equipment selection, installation and maintenance

6) Maintain expert level of understanding of GD&T

7) Lead investigations to determine root cause, development of corrective action plans, verification and effectiveness activities

8) Lead projects, teams and complex product transitions

9) Provide mentorship and support to team members

10) Develop quality standards and processes related to customer specifications and process improvement

11) Communicate with customers, suppliers and other resources to achieve the objectives

12) Work with customers to understand product specifications and satisfies any quality related issues and concerns

13) Evaluate process stability and capability

14) Analyze processes and procedures to ensure that they fit organization’s quality standards

15) Ensure quality processes and procedures comply with internal SOPs

16) Assist with regulatory audits

17) Perform inspections and sets quality assurance testing models for analysis of raw materials, materials in process and finished products

18) Write detailed work instruction-level documents for quality and related areas

19) Train personnel in these instructions and other technical process controls

20) Quarantine, document and evaluate products and materials

21) Ensure that control plans and associated documentation are implemented effectively and maintained

22) Monitor and report on quality-related key performance indicators

23) Ensure the compliance and assist with adherence to quality management system

24) Write product test procedures and perform IQ, OQ and PQ protocols


Critical Requirements


1) A university degree is required. Although all candidates are welcome and encouraged to apply, preference will be given to those with degrees in a relevant field

2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)

3) Recent experience in the medical device industry is strongly preferred

4) Preference will be given to candidates with recent experience in quality engineering


If you are qualified and this seems like just the right opportunity to take your career to the next level, please apply – we want to hear from you!


Compensation and Other Details


Base Salary: Highly competitive package, commensurate with experience

  • Published on 14 Jan 2022, 11:47 AM