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You will be updated with latest job alerts via emailWe are seeking a selfdriven and continuous improvementfocused Quality Engineer I to join our Utica NY based Quality Engineering team. In this role you will work crossfunctionally to provide support to all functions for the design procurement assembly test manufacturing validation and distribution of medical devices processes and quality systems. This role will be supporting the supplier quality and processes. At CONMED we do things the right way. Our Quality Engineering team comprises passionate engineers and specialists who maintain programs and systems that ensure adherence to quality standards and expectations. This teams work is crucial in ensuring that our products are accessible to our healthcare customers around the world. This is an onsite position in Utica NY.
Responsibilities:
Investigate process and product issues as assigned by supervisor. Work with other functional groups to resolve difficult quality problems on products processes or materials used in manufacturing operations.
Assist in the development and implementation of product and process quality plans and inspection and testing strategies. Provide support for the implementation of process and product qualifications and validations.
Assist in the development and implementation of quality programs including analyzing and problem solving including proposing solutions/improvements as well as of these proposals.
Assist in the daytoday operations of the Corrective and Preventive Actions system and assist in the implementation and effectively determination of corrective and preventive action plans.
Provide direction on test methods and protocols to ensure verification activity is adequate to assure the safety and efficacy of the device for product development and quality conformance teams.
Assist in the performance of supplier capability assessments analyzing performance data facilitating problemsolving activities and developing suppliers in quality tools and techniques. Auditing and qualifying new suppliers performing VA/VE efforts with and solving process and design problems with suppliers.
Assist product development teams. Develop and implement product quality plans verification/validation protocols and reports and other documents and systems by creating quality specifications and quality plans in conjunction with other product development team members.
Maintain quality system processes and procedures to ensure compliance to all domestic and international standards or requirements.
Perform investigations and resolution of validation failures process deviations abnormal results complaints and quality inquiries and other quality performance indicators as applicable.
The Quality Engineer is responsible for analysis and decision making that has major impact on system and product compliance and the organizations ability to meet customer and regulatory requirements.
Requirements:
Bachelors degree
02 years of experience in medical mechanical or electrical production test or inspection environment
Preferred Experience:
Basic understanding of problem solving and quality improvement tools and techniques.
Travel Expectations 020
This positionis not eligible for employervisa sponsorship.
Disclosure as required by applicable law the annual salary range for this position is $62000$97000. The actual compensation may vary based on geographic location work experience education and skill level. The salary range is CONMEDs good faith belief at the time of this posting.
Benefits:
CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.
Know someone at CONMED Have them submit you as a referral before applying for this position to be eligible for our Employee Referral Program incentives!
CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. The Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment.
Colorado Residents: In any materials you submit you may redact or remove ageidentifying information such as age date of birth or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
If you feel you need a reasonable accommodation pursuant to the ADA you are encouraged to contact us atoption #5.
Full-Time