QC Supervisor

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Location :
Irvine, California

Expiry Date :
Mon, 14 Jun 2021 23:59:59 GMT

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Description :
Job Description Summary Job Description Responsible for planning and managing the Quality Control function including receiving inspection, in-process inspection, and release inspection. Directs the workflow of the Quality Control group and reports on the status and results of inspection and test activities. Manages QC department and overall expectations pertaining to setting accurate schedules and allocating resources. – Ensures department is adequately resourced and trained to perform jobs effectively. – Directly supervises QC staff including coaching and developing to enable maximum performance and individual employee growth, providing regular performance review and feedback and using corrective action as necessary. – Ensures delivery against QC department goals and objectives, i.e. meeting commitments and coordinating overall inspection schedule. – Encourages a team atmosphere and leads by example. Responsible for the execution, maintenance, and periodic review of inspection process and procedures. – Manages QC staff to ensure that inspection activities are compliant to documented procedures. – Reviews inspection procedures to ensure compliance with regulatory requirements. – Develops metrics to identify and prioritize activities pertinent to process control, risk reduction, and cost improvement. – Supports technical aspects of the inspection process, including method troubleshooting and statistics. Responsible for product control and release. – Ensures batch records are reviewed and approved. – Ensures nonconforming and/or suspect material is appropriately documented, segregated, and reported to facilitate effective disposition. – Manages material transactions in regards to quality control testing and product release. Qualifications: – A minimum of 7 years quality control experience and a minimum of 2 years recent supervisory experience. – At least 5 yearsmedical device experience. – A B.S. Degree in Engineering, Quality Assurance, Biology, Microbiology, or related discipline is desirable – Applied knowledge of the requirements of FDA QSR and ISO 13485. – Ability to manage and prioritize multiple projects and deliverables while clearly communicating status and identifying obstacles. – Must have a positive attitude with excellent communication, negotiation and interpersonal skills to maintain a team-oriented environment and maintain critical relationships with team members, colleagues from different functions, and the sites management team. – Ability to thrive under challenging deadlines and in an energetic environment. – Must have a desire for achieving excellence in customer satisfaction, process and product quality and reliability. – Must have hands-on experience with process improvement projects. – Must have the technical expertise to drive troubleshooting and failure investigations. – Experience with sterilization and environmental monitoring is a plus. – Experience in developing and/or transferring inspections and test methods is a plus. Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. #LI-PRO Primary Work LocationUSA CA – Irvine Neomend Additional Locations Work ShiftNA (United States of America)