Overview


Título del trabajo: Quality Assurance Technician Iii

Compañía: Confluent Medical Technologies

Descripción de funciones: Job Description :Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.At Confluent, we are committed to our values of teamwork, innovation, accountability, integrity, leadership, and customer focus, and we invest in a team who represents these values. Every member of our team plays a critical role in delivering life-saving medical devices through innovative materials science, engineering, and manufacturing. We are the medical device industry’s most trusted partner, and we accomplish this with an organization focused on safety, efficiency, and customer satisfaction.We are looking for a Quality Assurance Technician III to join our team in Costa Rica. If you enjoy working in a fast-paced environment and making an impact on our life-saving work, this may be a good fit for you! As a uniquely qualified candidate, you will:SUMMARY: Works on problems and projects of limited scope where analysis of situation or data requires a review of identifiable factors. Participates in decisions on scope of work, supports selection of equipment, provides and develops solutions to problems of limited scope. Must be able to accomplish simple and general assignments. May provide technical guidance to quality inspectors and operators.ESSENTIAL DUTIES AND RESPONSABILITIES include the following. Other duties may be assigned.Supports the development, application, maintenance to quality standards for processing materials/products into partially or finished products.Contributes in the designs and implementation of methods and/or procedures for inspecting, testing and evaluating the precision and accuracy of measurement systems and test methods, products and/or production equipment. Analyzes reports and returned products and recommends corrective action.Prepares documentation for inspection/testing procedures.Plans and conducts work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria. Devises new approaches to problems encountered. Independently performs most assignments with instructions as to the general results expected. Receives technical guidance on unusual or complex problems and supervisory approval on proposed plans for projects. Plans, schedules, conducts, and coordinates detailed phases of engineering work a in tasks of moderate scope. Support quality engineering with work which involves conventional engineering practice but may include a variety of complex features such as reducing sampling plans and using statistics to reduce the issues coming across.Support quality engineering in DCOs, ECOs and running validation protocols and reports.May technically supervise or coordinate the work of inspectors and operators or others who assist in specific assignments.Be aware and work to achieve the Key Performance Indicators (KPIs). Practices company safety, quality policies and procedures, actively requires conformance. May require conducting internal audits. Support in root cause investigations.Support internal and external audits, war room others.Other duties in the Quality Assurances area.EDUCATION and/or EXPERIENCE:Technical degree (i.e from a Technical High School or INA)Advanced college studies in engineering or related.Also 4-5 years of experience in medical industry, with minimum 3 years of experience in the Quality departmentIntermediate English level (written and reading)COMMENTS: This position description is an outline of the major recurring responsibilities of the job. It is not intended to be all-inclusive of the work to be performed. The incumbent(s) will typically perform other related job objectives, special assignments and less significant responsibilities.

Ubicación: Alajuela

Fecha del trabajo: Sat, 04 May 2024 22:59:21 GMT