adecco is seeking a senior quality engineer for our client, a global medical manufacturer, located in bridgeport, ct. the senior quality engineer is responsible for the planning, design, and implementation of quality control/quality assurance programs for the manufacturing process and product. with over a dozen locations in a growing industry, our client offers extensive opportunities to grow and advance your career.
essential duties and key responsibilities:
develop and execute quality engineering tests, validation, and qualification protocols to include procedures, spec sheets and sampling plans utilizing customer’s designs and specifications.
software validation
conduct process monitoring and measurement using applicable trend analysis tools to measure customer satisfaction, non-conforming material, and customer complaints.
perform analysis of test and inspection results using statistical software.
inspection methods planning to include development and implementation of gages and gauging systems for use by manufacturing and inspection personnel.
implement statistical process control techniques including process capability, gage, gr&r studies.
interface with customers, suppliers and internal departments in matters concerning quality; including advanced quality planning, product specification development, sterilization validation, shelf-life testing, product labeling.
develop and implement process control plans, inspection plans and related work instructions
support regulatory affairs as required in matters concerning regulatory compliance and regulatory audits.
investigate customer complaints and product failures and recommend corrective actions.
perform training duties for inspectors and manufacturing personnel as required, including gmp training.
perform internal and supplier quality system audits.
ensures compliance with the organization standards for cost control, waste reduction, quality, safety, on-time delivery.
education and/or experience
engineer has bachelor’s degree from four-year college or university in mechanical or industrial engineering or equivalent and a minimum of 4-5 years’ quality experience to include qc-qa auditing in a manufacturing environment, preferably medical device manufacturing.
skills, abilities and other requirements
detailed knowledge of principles and practices of quality engineering.
ability to think ahead.
kaizen and lean manufacturing techniques
high attention to detail
solid analytical skills
excellent interpersonal and communication skills to work with vendors, customers, and associates.
effective organization skills
ability to multi-task in a fast-paced environment and manage multiple priorities
ability to solve practical problems and deal with a variety of changing situations
quality orientation
knowledge of osha, ansi, and related safety regulations
ability to apply advanced mathematical concepts
computer proficient in microsoft office, excel, minitab, or other statistical analysis software.
proficient knowledge of ansi/asme, y14.5m dimensioning and tolerance.
if you meet the above qualifications and would like to apply for this position, please click apply now and upload your most current resume or you may email your resume to our recruiter, michael ramsden at michael.ramsden@adeccona.com. please include the job title on the subject line of any e-mail. be sure to include your contact number.
questions regarding this position can be addressed via email. thank you in advance for applying, however, only qualified candidates will be contacted.
equal opportunity employer/veterans/disabled
the company will consider qualified applicants with arrest and conviction records
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United States, Bridgeport ,Connecticut
2022-06-20
2022-07-20
1619858
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