Quality Manufacturing Engineer 3
Philips
Fecha: hace 2 semanas
ciudad: Alajuela, Alajuela
Tipo de contrato: Tiempo completo

Job Title
Quality Manufacturing Engineer 3
Job Description
Quality Manufacturing Engineer 3
The Product Quality Engineer 3 will work primarily with Product Industrialization Engineering, manufacturing engineering and R&D in support to the manufacturing Product Trasnfers, Design Changes and production sustaining activities, aditionally will provide support of product inspections, and product and process compliance to established procedures and will take corrective and preventive action as required by procedures to support the continued operation of the Costa Rica. Also will provide coaching and guidance to Product Quality Engineers 1 ans 2 for PQE topics related to Risk Management, Process Validacion, Quality Planning, CAPA, NCR, Design Changes, and other PQE related topics.
Lead a group of direct report (Quality Technicians or Engineers) as required.
You are responsible for
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations
This role is an onsite role/Administrative shift
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
Quality Manufacturing Engineer 3
Job Description
Quality Manufacturing Engineer 3
The Product Quality Engineer 3 will work primarily with Product Industrialization Engineering, manufacturing engineering and R&D in support to the manufacturing Product Trasnfers, Design Changes and production sustaining activities, aditionally will provide support of product inspections, and product and process compliance to established procedures and will take corrective and preventive action as required by procedures to support the continued operation of the Costa Rica. Also will provide coaching and guidance to Product Quality Engineers 1 ans 2 for PQE topics related to Risk Management, Process Validacion, Quality Planning, CAPA, NCR, Design Changes, and other PQE related topics.
Lead a group of direct report (Quality Technicians or Engineers) as required.
You are responsible for
- Responsible for leading quality engineering activities like:
- Designing Quality plans, overseeing the execution of Quality Plans, assessing complex software designs and reviewing test and other complex performance data, analyses market feedback.
- Lead complex root cause analysis and complex Quality problem solving.
- May also provide other Quality engineering support, including assisting organizational units in leading resolution of Quality engineering deficiencies.
- Seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways.
- This job is the fully qualified, career-oriented, journey-level position.
- Has knowledge of company products and services.
- Frequently interacts with subordinate engineers customers, and/or functional peer group normally involving matters between functional areas, other company divisions or units, or customers and the company. Often must lead a cooperative effort among members of a project team.
- Works on issues where analysis of situations or data requires an in-depth knowledge of organizational objectives.
- Implements strategic improvements when selecting methods, techniques, and evaluation criteria for obtaining results.
- Establishes and assures adherence to budgets, schedules, work plans, and performance requirements.
- This position is responsible for managing a part of a business process or function.
- Responsible for results, including costs, methods and staffing.
- Probably has budget responsibilities.
- Bachelor's degree in a Technical, Science, or Engineering discipline strongly preferred or Equivalent years of experience in manufacturing industry.
- Master Degree is a plus.
- 5+ year of experience in Quality or Manufacturing or a combination of equivalent job experience in related field and in Quality Engineering related activities. Working knowledge of appropriate global medical device or product regulations, requirements, and standards.
- Proven knowledge and application of applicable regulations for Medical Device manufacturing. The ideal candidate will bring hands-on experience in people management, including performance reviews, career development, and team engagement.
- Proven ability to understand and interpret established quality system requirements and provide advice to project teams and the organization in general on how to remain compliant to requirements during execution
- Strong and proven knowledge of statistical methods and the use of standard quality tools (e.g. flowcharts, Pareto charts, cause and effect diagrams, control charts, scatter diagrams, regression analysis, affinity diagrams, etc). Knowledge in General Principles Software Validation and Part 11 Knowledge in software life cycle
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations
This role is an onsite role/Administrative shift
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
- Learn more about our business.
- Discover our rich and exciting history.
- Learn more about our purpose.
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