Quality Engineer II

JOB TITLEQuality Operation Engineer II DEPARTMENTQuality Engineering JOB CODESExempt MAIN PURPOSE OF JOB AND OBJECTIVESPlease 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 to maintain 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 product along with product risk assessment and perform product failure investigations. Drives Supplier and Production Quality improvements, including efficiency and productivity improvements while maintaining compliance. POSITION IN ORGANISATIONPosition in organization can be found on the Organizational Chart via the company intranet.KEY DUTIESParticipates in the nonconformance process to ensure timely completion of documentation stages Identifies, Reports and Monitors Nonconforming events for the areas of responsibilityPerforms product or process failure investigations and implements corrective and preventive actions to prevent reoccurrenceInteracts 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 assignmentsApplies statistical tools to analyze data and identify root cause and problem resolutionCollaborates with Manufacturing, Product Support and R&D to support products for design and process improvements, and new equipment installationsRecommends 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 preventionPerform and lead risk assessment exercises in support of validation activitiesAdditionally, this role may also have some or all the following responsibilities (based on specific role within the organization):Drive Quality Systems improvement and implementation projectsOversees the Nonconformance process to ensure timely completion of documentation stages and drives monthly meetingsPrepare, review, execute, and summarize validation protocols (IQ, OQ, PQ)Drive supplier quality activities as directed per line managerDIMENSIONS & LIMITS OF AUTHORITYCOMPANYREQUIREMENTSMust work within requirements of company handbook and policy statementsNote: Company Handbook, Policy Statement and Authorization of Limits do not form part of the quality systemQUALITYREQUIREMENTSMaintain awareness of the relevance and importance of activities performed and how they contribute to the achievement of quality objectivesAlways Work within the QMS, ensure accurate completion of records and highlight issues to immediate supervisor any issues affecting qualityResponsible to ensure facility, processes and documentation always remain in a state of audit readinessEH&S REQUIREMENTSTake care of your own health and safety and that of others who may be affected by your actionsWork co-operatively to highlight issues affecting Environmental Health and SafetyQUALIFICATIONS & EXPERIENCEMinimum Skills & Capabilities:Works with all levels within the company.Ability to organize and conduct multiple, parallel tasksExcellent Written and Verbal CommunicationUnderstanding of quality system regulations (ISO13485, 21CFR820)Ability to interact with all levels within organizationAnalytical skills for compiling and analyzing dataMechanically inclined Knowledge of DOE, SPC, Gage R&R, and sampling plansComputer and software skills Ability to motivate others and improve efficiencySix Sigma Certification a plusASQ Quality Engineer Certification a plusStatistics and data analysisMinimum Knowledge & Experience required for the position:Bachelor’s degree in a technical discipline (Mechanical/Biomedical/Electrical engineering), or equivalent, with a minimum of 8 years of experience in medical device quality assurance.Minimum 3 years’ experience in Manufacturing Engineering or Quality Engineering with preference having validation experienceWorking knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO) - ISO 13485 and ISO 14971).Understanding of required standards / regulations impacting Medical Devices.Leadership ability and organizational skills.Strong team-oriented professional with good interpersonal skills who is hands-on with a high energy approach to work.Must have experience handling nonconforming eventsSAP knowledge is a plus