Quality - Quality Engineer 3 at Viant

, , Costa Rica -

Full Time

Start Date

Immediate

Expiry Date

18 Apr, 26

Salary

0.0

Posted On

18 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Engineering, Process Validation, Root Cause Analysis, Statistical Techniques, Risk Management, Six Sigma, Lean Manufacturing, Project Management, Interpersonal Skills, Analytical Skills, Problem Solving, Decision Making, Metrology, Documentation, Training, Auditing

Industry

Medical Equipment Manufacturing

Description

This is a full-time position to work Monday-Friday daily hours in our Heredia Site, located in Zona Franca Metropolitana. Remote work might be allowed based on business needs. Our Quality Engineers 3 provide quality engineering support to the development and production of Class I, II and III (as applicable) Medical Devices. Represent Quality in production process efforts, quality planning, process validations, FMEA and Risk Analysis, support new product development activities, maintain and manage quality compliance and supplier quality management. Support finished goods variance investigation and resolution, complaint investigation, process improvement and quality assurance testing methodology. Participate in or lead Corrective/Preventive Action initiatives. Support internal/ external and suppliers audit, vendor qualification and training programs. Participate in Quality/ Business initiatives including business process improvement activities, documented Quality System re-architecture and other cross-functional projects. Principal Responsabilities: Prepare and update quality documents and any applicable documentation required to sustain the manufacturing process, system or NPI projects, including but not limited to documentation linked to the Device Master Records and Device History Records. Execute reviewing / approval of any documentation created / updated by the Manufacturing Engineering department (or other) required to sustain the manufacturing process or quality systems. Support in analysis, review and implementation of new methodologies, processes, tools that contribute to the improvement on the manufacturing process, quality systems or supplier improvements. Checks, provides support and executes initiation / investigation for NCs, Complaints, Calibration, SCARs and Environmental Monitoring. Provide follow up to actions generated from corrective and preventive plans. Performs other duties, tasks, or projects at the direction of the immediate supervisor or other teammates. Maintain and follow up CAPA and supplier files. (Quality Systems and Supplier Engineer only). Support in the execution of qualifications (IQs/OQs/PQs/PPQs/TMVs) with an approved protocol; gather data and analysis results for completing the corresponding report. Assure that all laboratory equipment is in compliance to perform the analysis and testing activities (quality labs, calibration, microbiology and incoming). Participates in all the readiness activities required to receive Internal / External / Customer / Suppliers Quality System Audits. Collaborate in the elaboration of risk management documentation such as Risk Management Plan / Report and Process FMEAs. Review protocols and reports for IQ, OQ, PQ, PPQ and TMV; as well as any other document related to validation. Prepare respective validation protocols and reports for low and moderate complexity qualifications or participate in the approval of them. Participates on the definition of validation strategies. Elaboration of Validation Master Plans to define / document all the validation strategy required to implement a new product / process or change a current one. Also, elaborate the Validation Master Plan Closure once all the activities have been executed Read and interpret technical drawings provided by the customer and elaborates the related documentation such as of QA Specs, Control Plans, other. Elaboration of work instructions, automated routines or any other document required to execute inspections. Also, validate these inspections through TMV Protocols and TMV Reports.. Participate in the communications with the customers including projects, product/process transfers, weekly sustaining report out meetings, Quarterly Business Reviews, other. Provide new hire introduction sessions. (Quality Process and Quality Systems Engineer only). Create quarterly suppliers' evaluation, scorecards. (Supplier Quality Engineer only). Purchasing control of approved suppliers through the document change control process. (Supplier Quality Engineer only). Coordinate the development of new processes inspections by interfacing with personnel from product design and development, quality assurance, production, manufacturing, process/assembly technology and external vendors / customers. Participate in the preparation of quality metrics required for Management Review, Operations Review or Quality Metrics meetings. Review drawings, analyze tooling, and recommend improvements leading to increase productivity, quality, and safety for new or existing manufacturing processes. Coordinate and carry out qualification and validation activities for new products, processes, changes and transfers as per FDA regulations (IQ, TMV, OQ, PQ and Quality Plans). Prepare respective validation protocols and reports for moderate and high complexity qualifications or participate in the approval of them. Executes investigations for audit non-conformances, complaints and Corrective and Preventive Actions (CAPA) to correct a problem presented in the quality system or the manufacturing process. Responsible for the elaboration of risk management documentation such as Risk Management Plan / Report and Process FMEAs. Become supervisor of Quality Inspectors / Technicians / Specialists and be responsible for the task's assignation / coordination of these personnel in charge. Train Quality Assurance Inspectors and manufacturing personnel in understanding of procedures, specifications, environmental controls, etc. Act as a quality system internal auditor. Participate in communications with the customers including weekly sustaining report out meetings, QBRs, projects meetings, other. Required Knowledge & Education Minimum education required to perform duties: Bachelor degree in Engineering or Science (such as Pharmacy, Microbiology, Physics and Chemistry). Bilingual English/Spanish – Advanced English level (written and spoken). Knowledge of applicable regulations for the medical device industry (FDA, ISO, other.) Knowledge and application of risk management (PFMEA’s). Knowledge of process validation. Knowledge in root cause analysis tools. Knowledge and application of statistical techniques (Sampling Plans, Gage R&R’s, Hypothesis Test, Statistical Process Control {SPC}, Process Capability Studies, Design of Experiments {DOE}). Knowledge of Minitab statistical software. Knowledge of Six Sigma Methodology and Lean Manufacturing. Preferred Knowledge & Education: Proficiency in the use of MS Project Knowledge in software validation Certified Quality Engineer or Green Belt Certified Auditor Job Experience: At least 2 years' work experience in manufacturing environment. Project Management experience. Experience within the medical device manufacturing or pharmaceutical fields, or any other highly regulated industry (i.e. food, aerospace, etc.) is a plus. Skills / Competencies Good interpersonal skills and the ability to communicate orally and in writing. Self-motivated. Organized and able to manage multiple tasks and priorities. Must be able to read and understand specifications. Proficient in the interpretation of technical drawings. Must be able to work and effectively communicate with others. Highest ethical standards and professional integrity. Able to work independently. Teamwork oriented. All skills and competencies listed for categories 1 and 2. Effective planning and time management Customer oriented Results oriented Analytical Innovative Self-starter willing to take calculated risks. Demonstrated leadership and motivational skills. Problem Solving: Must be able to identify cause and effect relationships, analyze data and complete root cause analysis. Metrology: Capable of developing measuring procedures and test methods, selecting test equipment, measuring instruments and validating test methods. Decision making: Capable of making medium risk decisions for specific projects and situations. Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn. Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.

Responsibilities

Quality Engineers 3 provide quality engineering support for the development and production of medical devices, ensuring compliance and managing supplier quality. They participate in process validations, risk analysis, and corrective/preventive action initiatives.