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Job Requirements of Quality Investigator JR:
-
Employment Type:
Full-Time
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Location:
Caledonia, WI (Onsite)
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Quality Investigator JR
Bayone Solutions Inc
Caledonia, WI (Onsite)
Full-Time
Schedule: 8 am -4:30 pm with some flexibility for start time
Job Description: This position supports a wide array of activities related to: Supplier Management
Supplier Management Activities including: Supplier adds, supplier re-evaluations, supplier ratings, supplier corrective action management, supplier notification of change
Adherence to regulations - Assist with adherence to all Federal, State, and Local Regulations controlling the manufacture of medical devices.
Support the operation of Manufacturing and Quality activities in relation to compliance to Quality Standards.
Support the operation of the Quality System process related to Corrective/Preventive actions and product non-conformance control including: capturing data associated with product deviations, product non-conformances, CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement and reporting.
Requirements:
BS/BA in Physical Science or Engineering or 2 + years in medical device/Pharmaceutical industry
Recent graduates encouraged to apply.
Experience in Quality Assurance and/or other regulated industry or similar experience a plus.
Strong technical writing skills and general problem solving skills.
Manage multiple priorities and work with interruptions.
GLP and/or GMP experience a plus.
Medical Device knowledge a plus.
Requires Vision Assessment (20/20 near visual acuity & acceptable color vision).
Job Description: This position supports a wide array of activities related to: Supplier Management
Supplier Management Activities including: Supplier adds, supplier re-evaluations, supplier ratings, supplier corrective action management, supplier notification of change
Adherence to regulations - Assist with adherence to all Federal, State, and Local Regulations controlling the manufacture of medical devices.
Support the operation of Manufacturing and Quality activities in relation to compliance to Quality Standards.
Support the operation of the Quality System process related to Corrective/Preventive actions and product non-conformance control including: capturing data associated with product deviations, product non-conformances, CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement and reporting.
Requirements:
BS/BA in Physical Science or Engineering or 2 + years in medical device/Pharmaceutical industry
Recent graduates encouraged to apply.
Experience in Quality Assurance and/or other regulated industry or similar experience a plus.
Strong technical writing skills and general problem solving skills.
Manage multiple priorities and work with interruptions.
GLP and/or GMP experience a plus.
Medical Device knowledge a plus.
Requires Vision Assessment (20/20 near visual acuity & acceptable color vision).
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