Role : QC inspector/ Quality Control Inspector
Location: El Paso TX
Duration: 6 months
Looking for someone with 3-5 years of Experience
Description : Must Have Technical Functional Skills Perform incoming in process and final inspections of components sub-assemblies and or finished goods in accordance with approved inspection plans drawings and specifications. Conduct inspections using visual dimensional and functional methods utilizing calibrated measurement tools such as calipers micrometers and gauges. Ensure compliance with ISO 13485 FDA 21 CFR Part 820 and Medtronic Supplier Quality requirements. Accurately document inspection results in quality records travelers and or electronic quality systems in accordance with Good Documentation Practices (GDP).Identify document and escalate nonconforming material supporting containment actions and investigations. Support lot release activities and ensure full traceability of inspected materials. Participate in root cause analysis CAPA activities and continuous improvement initiatives as required. Support readiness for internal customer and regulatory audits. Collaborate with Manufacturing Engineering and Supplier Quality teams to resolve quality issues in a timely manner Roles Responsibilities Perform incoming in process and final inspections of components sub-assemblies and or finished goods in accordance with approved inspection plans drawings and specifications .Conduct inspections using visual dimensional and functional methods utilizing calibrated measurement tools such as calipers micrometers and gauges. Ensure compliance with ISO 13485 FDA 21 CFR Part 820 Accurately document inspection results in quality records travelers and or electronic quality systems in accordance with Good Documentation Practices (GDP).Identify document and escalate nonconforming material supporting containment actions and investigations .Support lot release activities and ensure full traceability of inspected materials. Participate in root cause analysis CAPA activities and continuous improvement initiatives as required. Support readiness for internal customer and regulatory audits. Collaborate with Manufacturing Engineering
Role : QC inspector/ Quality Control Inspector Location: El Paso TX Duration: 6 months Looking for someone with 3-5 years of Experience Description : Must Have Technical Functional Skills Perform incoming in process and final inspections of components sub-assemblies and or finished goods in accord...
Role : QC inspector/ Quality Control Inspector
Location: El Paso TX
Duration: 6 months
Looking for someone with 3-5 years of Experience
Description : Must Have Technical Functional Skills Perform incoming in process and final inspections of components sub-assemblies and or finished goods in accordance with approved inspection plans drawings and specifications. Conduct inspections using visual dimensional and functional methods utilizing calibrated measurement tools such as calipers micrometers and gauges. Ensure compliance with ISO 13485 FDA 21 CFR Part 820 and Medtronic Supplier Quality requirements. Accurately document inspection results in quality records travelers and or electronic quality systems in accordance with Good Documentation Practices (GDP).Identify document and escalate nonconforming material supporting containment actions and investigations. Support lot release activities and ensure full traceability of inspected materials. Participate in root cause analysis CAPA activities and continuous improvement initiatives as required. Support readiness for internal customer and regulatory audits. Collaborate with Manufacturing Engineering and Supplier Quality teams to resolve quality issues in a timely manner Roles Responsibilities Perform incoming in process and final inspections of components sub-assemblies and or finished goods in accordance with approved inspection plans drawings and specifications .Conduct inspections using visual dimensional and functional methods utilizing calibrated measurement tools such as calipers micrometers and gauges. Ensure compliance with ISO 13485 FDA 21 CFR Part 820 Accurately document inspection results in quality records travelers and or electronic quality systems in accordance with Good Documentation Practices (GDP).Identify document and escalate nonconforming material supporting containment actions and investigations .Support lot release activities and ensure full traceability of inspected materials. Participate in root cause analysis CAPA activities and continuous improvement initiatives as required. Support readiness for internal customer and regulatory audits. Collaborate with Manufacturing Engineering
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