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Talented Quality Engineer or Senior Quality Engineer, Medical Device Company
| Details |
Country: USA
Location: Connecticut-Stamford Statewide, CT
Total applied: 40 Salary/Wage:60,000.00 - 100,000.00 USD /yearPlus Bonus
Job Category:Quality Assurance/Safety
Relevant Work Experience:2+ to 5 Years
Location:Statewide, CT
Status:Full Time, Employee
Occupations:General/Other: Quality Assurance/Safety;Production Quality Assurance;Six Sigma/Black Belt/TQM
Career Level:Experienced (Non-Manager)
Relevant Work Experience:2+ to 5 Years
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Talented Quality Engineer or Senior Quality Engineer, Medical Device Company
As a Quality Engineer or a Senior Quality Engineer (with the strong possibility of promotion to Management) for the Outstanding Medical Device Company, you would be responsible for all aspects of quality in this fast paced medical device manufacturing plant and will help plan and/or direct all quality engineering activities for new product launches. You would work closely with the Engineering Team, the Plant Manager, and Manufacturing, on advanced quality planning to effectively bring new products from concept to production. You would enjoy competitive compensation and a generous benefits package that includes health, dental, 401k (with match), and tuition reimbursement. Relocation to this beautiful area is provided for the right candidate. (This TEAM works hard and plays hard)
KEY RESPONSIBILITIES: You would work with customers to ensure advanced quality plans including critical dimensions, control plans, process flow diagrams, SPC plans, FMEA’s, etc. are initiated during the earliest stages of each program. You would work with other Quality Engineers to ensure proper utilization of advanced quality planning tools consistent with ISO-TS procedures. You would help validate existing and new products through concept, design, development and transfer to Manufacturing Operations requirements.
KEY QUALIFICATIONS: You would have 2 to 20+ years of hands on experience in medical device quality assurance. It would be helpful if you were an ASQ Certified Quality Engineer, or are currently pursuing ASQ certification. Working knowledge in Design of Experiments (DOE), and ability to implement theories during qualification phases of new programs is preferred. Experience with Minitab or other statistical software strongly desirable in a medical or FDA regulated environment would be a strong plus. You would be able to identify problems and communicate solutions in a constructive and positive manner in a fast paced manufacturing environment.
If this seems like a fantastic opportunity in an area that you could grow both personally and professionally, then send your resume (In "Word") in complete confidence to the attention of Jim Clark. Email address is: themillenniumgroupus@yahoo.com
Note: Full relocation, 401K and all benefits provided for the right candidate!!
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