Senior Quality Assurance Engineer
| How to Apply for this Job |
Company: The Yaiser Group
Contact Name: DICK YAISER
- Email your resume (Click Here)
- Phone: 201 568 4745
Use one of the above methods to apply for this job.
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- Job ID:
- Date:06/27/2008
- Location:
- State:New Jersey
- Degree:B.S./B.A.
- Major:CHEM;ENGINEERING;BIOMEDICAL ENGINEERING;
- Current Professional Level:Experienced Staff Level
- Salary Range:$70,000 to $79,999
- This salary range was selected from the CareersInPharmaceutical.com salary data list. See the "Additional Salary" or contact the Recruiter for actual salary and benefits.
- Additional Salary/Compensation:
- YES
- Job Types:
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BIOMEDICAL/MEDICAL DEVICE(Device R&D), QUALITY ASSURANCE (Drug or Device), Six Sigma
Job Description
The Senior Quality Assurance Engineer will be responsible for supporting new product development and product maintenance through the application of QE skills. This requires the ability to handle multiple projects and tasks from product inception through product launch and maintenance. The incumbent will be responsible for assuring that the products meet the quality standards consistent with Corporate and Division policies, while meeting all design control requirements. The incumbent will interact with multiple plants, OEM suppliers, Distribution Centers and customers with emphasis on prevention of quality issues and quality improvement programs. The position directly interfaces with R&D, Marketing, Plant Engineering, Operations, Medical / Clinical and Supplier Management with emphasis on design requirements.
1) Develop methods to measure, validate and assure quality standards are achieved for applicable product lines. 2) Serve as a multi-functional team member establishing quality requirements and providing guidance in product development projects. 3) Serve as a multi-functional team leader for quality improvement teams assuring commitments and objectives are achieved with positive results. 4) Assess applicable systems assuring conformance to quality standards and compliance to regulatory requirements. 5) Maintains knowledge of product line, manufacturing process, current technological advances and industry standards for regulatory and product performance requirements, and share information as appropriate with applicable functions. 6) Lead and coordinate failure investigations for design issues.
1) BS in Engineering or Physical Science: Biomedical Engineering / Chemistry preferred (Emphasis on Molecular Diagnostics) 2) American Society of Quality Certified Quality Engineer : preferred 3) Minimum of 5 years experience in a regulated industry 4) Demonstrated application or implementation of statistical methods and, 5) Excellent team and interpersonal skills.6) Six Sigma Certification preferred.7) Understanding and proficiency with process validation.
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