Quality Inspection Supervisor, Olive Branch
Quality Inspection Supervisor, Olive Branch
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Olive Branch 38654, USA
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Posted: less than a week ago
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Description
Quality Inspection Supervisor
Position Summary Growth, Culture, People and Careers: this is the Teleflex Advantage. In this exciting role as a Quality Supervisor, you will have responsibility for leading teams through Quality System Transformation by defining and trending metrics. This role will lead multiple projects within a larger program with a focus on creating more usable and simpler to follow processes, reducing burden within our quality systems, and driving efficiency.Principal Responsibilities Manage, supervise, and prioritize Quality Inspector activity in support of routine testing, product release, incoming inspection, process non-conformances, etc. Assist in ensuring all lots of finished products distributed at the NADC meet all internal specifications, customer expectations, and regulatory requirements.Provide training development where needed. Assist as a technical expert in relevant technical issues, protocols, SOPs, methods, etc. Manage and implement cost improvement projects within the department and in support of internal customers. Track, report,&improve key quality indicators for quality compliance, productivity, and efficiency. Provides input to annual spending and headcount budgets. Manages and acts as the contact for functional groups, nonconforming products, and production issues Performs Non-Conformance (NC) investigations and Corrective Action / Preventative Actions (CAPA).Participates in FDA inspections, ISO certifications, surveillance audits, etc. Manages performance review for direct reports within assigned time frames. Coordination and/or complete calibration of test equipment and gauges. Maintain calibration records and work with calibration vendors. Assist with determining gauge requirements.Administer customer complaint investigations and documentation as needed. Assist in enforcing all local, state, federal, and safety regulations/policies/procedures. Complies with all policies/procedures/practices through consistent application of sound Quality Assurance principles. Ensures compliance with quality policies/procedures/practices.Provide other departmental support as requested by the immediate supervisor. Adhere to and ensure compliance with Teleflex's Code of Conduct, all Company policies, rules, procedures, and housekeeping standards. Education / Experience Requirements Bachelor's degree required, technical degree preferred, or higher degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, and pharmacology), math, engineering, or medical fields.5-7 years of quality assurance experience in a manufacturing or distribution environment within the Medical Device Industry preferred. Minimum three years of supervisory experience, preferred. Specialized Skills / Other Requirements Minimum three years of experience with US and international medical device regulations, standards, and guidance documents. Including:21 CFR 820 US FDA Quality System Regulations. ISO 13485 Medical devices
Quality management system
requirements for regulatory purposes. Project Management skills and experience. Must have strong written and verbal communication skills. Must be able to effectively present at staff and department meetings. Knowledge of MS Office Suite.
Position Summary Growth, Culture, People and Careers: this is the Teleflex Advantage. In this exciting role as a Quality Supervisor, you will have responsibility for leading teams through Quality System Transformation by defining and trending metrics. This role will lead multiple projects within a larger program with a focus on creating more usable and simpler to follow processes, reducing burden within our quality systems, and driving efficiency.Principal Responsibilities Manage, supervise, and prioritize Quality Inspector activity in support of routine testing, product release, incoming inspection, process non-conformances, etc. Assist in ensuring all lots of finished products distributed at the NADC meet all internal specifications, customer expectations, and regulatory requirements.Provide training development where needed. Assist as a technical expert in relevant technical issues, protocols, SOPs, methods, etc. Manage and implement cost improvement projects within the department and in support of internal customers. Track, report,&improve key quality indicators for quality compliance, productivity, and efficiency. Provides input to annual spending and headcount budgets. Manages and acts as the contact for functional groups, nonconforming products, and production issues Performs Non-Conformance (NC) investigations and Corrective Action / Preventative Actions (CAPA).Participates in FDA inspections, ISO certifications, surveillance audits, etc. Manages performance review for direct reports within assigned time frames. Coordination and/or complete calibration of test equipment and gauges. Maintain calibration records and work with calibration vendors. Assist with determining gauge requirements.Administer customer complaint investigations and documentation as needed. Assist in enforcing all local, state, federal, and safety regulations/policies/procedures. Complies with all policies/procedures/practices through consistent application of sound Quality Assurance principles. Ensures compliance with quality policies/procedures/practices.Provide other departmental support as requested by the immediate supervisor. Adhere to and ensure compliance with Teleflex's Code of Conduct, all Company policies, rules, procedures, and housekeeping standards. Education / Experience Requirements Bachelor's degree required, technical degree preferred, or higher degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, and pharmacology), math, engineering, or medical fields.5-7 years of quality assurance experience in a manufacturing or distribution environment within the Medical Device Industry preferred. Minimum three years of supervisory experience, preferred. Specialized Skills / Other Requirements Minimum three years of experience with US and international medical device regulations, standards, and guidance documents. Including:21 CFR 820 US FDA Quality System Regulations. ISO 13485 Medical devices
Quality management system
requirements for regulatory purposes. Project Management skills and experience. Must have strong written and verbal communication skills. Must be able to effectively present at staff and department meetings. Knowledge of MS Office Suite.
Highlights
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Company nameTeleflex
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Job positionQuality Inspection Supervisor
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