Terumo Aortic
Overview
Talent Acquisition Specialist at Terumo Aortic JOB TITLE Senior Quality Operations Engineer DEPARTMENT Quality Operations JOB CODES Exempt MAIN PURPOSE OF JOB AND OBJECTIVES Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Responsible for supporting the quality engineering operations of receiving inspection, in-process and finished product and maintaining processes and methods in accordance with the company standards. Reporting on the performance of the assigned quality areas. Responsible for maintaining regulatory compliance. Develops quality standards and controls. Develops product and process qualifications/validation protocols/reports for new products and existing manufacturing production lines. Advises company management on quality assurance requirements. Review non-conforming products along with product risk assessment and perform product failure investigations. Drives Supplier and Production Quality improvements, including efficiency and productivity improvements while maintaining compliance. Key Duties
Participates in the nonconformance process to ensure timely completion of documentation stages. Identifies, Reports and Monitors Nonconforming events for the areas of responsibility. Performs product or process failure investigations and implements corrective and preventive actions to prevent reoccurrence. Interacts with cross-functional teams to resolve quality issues. Quality control, product release authorizations, and quarantine of all suspect or discrepant product. Develops Quality Instructions and Quality Standards. Support in the development, validation, and implementation of Test Methods. Suggests, implements, reviews, and approves engineering changes to support product life cycle. Provides adequate QA support to the assigned areas and responds to Internal Audits, and takes actions as appropriate based on CAPAs, Complaint investigations, Nonconforming events, etc. Supports the Corrective and Preventive Action (CAPA) System for Quality Operations-related activities. Applies knowledge in Quality Systems to execute overall project assignments. Applies statistical tools to analyze data and identify root cause and problem resolution. Collaborates with Manufacturing, Product Support and R&D to support products for design and process improvements, and new equipment installations. Recommends decisions on administrative or operational matters and ensures Quality Assurance(s) effective achievement of objectives. Ensures quality system compliance for areas of responsibility. Serve as a technical resource for assessing validation requirements, solving test related problems, and developing strategies for problem prevention. Perform and lead risk assessment exercises in support of validation activities. Additionally, this role may also have some or all the following responsibilities (based on specific role within the organization): Drive Quality Systems improvement and implementation projects. Oversees the Nonconformance process to ensure timely completion of documentation stages and drives monthly meetings. Prepare, review, execute, and summarize validation protocols (IQ, OQ, PQ) Qualifications & Experience
Minimum Skills & Capabilities: Works with all levels within the company. Ability to organize and conduct multiple, parallel tasks. Understanding of quality system regulations (ISO13485, 21CFR820) Ability to interact with all levels within organization. Analytical skills for compiling and analyzing data. Mechanically inclined Knowledge of DOE, SPC, Gage R&R, and sampling plans Computer and software skills Ability to motivate others and improve efficiency. ASQ Quality Engineer Certification a plus Statistics and data analysis. Minimum Knowledge & Experience: Bachelors degree in a technical discipline (Mechanical/Biomedical/Electrical engineering), or equivalent, with a minimum of 12 years of experience in medical device quality assurance. Minimum 5 years experience in Manufacturing Engineering or Quality Engineering with preference having validation experience. Working knowledge of FDA 21 CFR 820 and ISO 13485/14971. Understanding of standards/regulations impacting Medical Devices. Leadership ability and organizational skills. Strong team-oriented professional with hands-on, high-energy approach. Experience handling nonconforming events. SAP knowledge is a plus. Seniorities & Employment Seniority level: Mid-Senior level Employment type: Full-time Job function & Industries
Job function: Quality Assurance, Manufacturing, and Product Management Industries: Manufacturing and Pharmaceutical Manufacturing
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Talent Acquisition Specialist at Terumo Aortic JOB TITLE Senior Quality Operations Engineer DEPARTMENT Quality Operations JOB CODES Exempt MAIN PURPOSE OF JOB AND OBJECTIVES Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Responsible for supporting the quality engineering operations of receiving inspection, in-process and finished product and maintaining processes and methods in accordance with the company standards. Reporting on the performance of the assigned quality areas. Responsible for maintaining regulatory compliance. Develops quality standards and controls. Develops product and process qualifications/validation protocols/reports for new products and existing manufacturing production lines. Advises company management on quality assurance requirements. Review non-conforming products along with product risk assessment and perform product failure investigations. Drives Supplier and Production Quality improvements, including efficiency and productivity improvements while maintaining compliance. Key Duties
Participates in the nonconformance process to ensure timely completion of documentation stages. Identifies, Reports and Monitors Nonconforming events for the areas of responsibility. Performs product or process failure investigations and implements corrective and preventive actions to prevent reoccurrence. Interacts with cross-functional teams to resolve quality issues. Quality control, product release authorizations, and quarantine of all suspect or discrepant product. Develops Quality Instructions and Quality Standards. Support in the development, validation, and implementation of Test Methods. Suggests, implements, reviews, and approves engineering changes to support product life cycle. Provides adequate QA support to the assigned areas and responds to Internal Audits, and takes actions as appropriate based on CAPAs, Complaint investigations, Nonconforming events, etc. Supports the Corrective and Preventive Action (CAPA) System for Quality Operations-related activities. Applies knowledge in Quality Systems to execute overall project assignments. Applies statistical tools to analyze data and identify root cause and problem resolution. Collaborates with Manufacturing, Product Support and R&D to support products for design and process improvements, and new equipment installations. Recommends decisions on administrative or operational matters and ensures Quality Assurance(s) effective achievement of objectives. Ensures quality system compliance for areas of responsibility. Serve as a technical resource for assessing validation requirements, solving test related problems, and developing strategies for problem prevention. Perform and lead risk assessment exercises in support of validation activities. Additionally, this role may also have some or all the following responsibilities (based on specific role within the organization): Drive Quality Systems improvement and implementation projects. Oversees the Nonconformance process to ensure timely completion of documentation stages and drives monthly meetings. Prepare, review, execute, and summarize validation protocols (IQ, OQ, PQ) Qualifications & Experience
Minimum Skills & Capabilities: Works with all levels within the company. Ability to organize and conduct multiple, parallel tasks. Understanding of quality system regulations (ISO13485, 21CFR820) Ability to interact with all levels within organization. Analytical skills for compiling and analyzing data. Mechanically inclined Knowledge of DOE, SPC, Gage R&R, and sampling plans Computer and software skills Ability to motivate others and improve efficiency. ASQ Quality Engineer Certification a plus Statistics and data analysis. Minimum Knowledge & Experience: Bachelors degree in a technical discipline (Mechanical/Biomedical/Electrical engineering), or equivalent, with a minimum of 12 years of experience in medical device quality assurance. Minimum 5 years experience in Manufacturing Engineering or Quality Engineering with preference having validation experience. Working knowledge of FDA 21 CFR 820 and ISO 13485/14971. Understanding of standards/regulations impacting Medical Devices. Leadership ability and organizational skills. Strong team-oriented professional with hands-on, high-energy approach. Experience handling nonconforming events. SAP knowledge is a plus. Seniorities & Employment Seniority level: Mid-Senior level Employment type: Full-time Job function & Industries
Job function: Quality Assurance, Manufacturing, and Product Management Industries: Manufacturing and Pharmaceutical Manufacturing
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