Process Quality Engineer 2

Job title:The Process Quality Engineer 2 will work primarily with manufacturing processes and engineering counterparts in Advanced Engineering or Design Assurance in 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 site manufacturing lines as well as the introduction of new manufacturing line processes, or transfer of existing processes from other facilities into Costa Rica.

Your role:

• Supports operations performance monitoring, risk assessment, reporting, improvement and development, aids with improvement programs in factory, and supports analytical testing and
• Supplier Quality Engineering (SQE), Supplier Quality Assurance (SQA) and Purchasing.
• Coordinates timely quality engineering and quality assurance tasks, aids in ensuring manufacturing quality systems are maintained, and helps in completion of New Product Introduction (NPI) and product transfers in factory.
• Possesses working knowledge of generic products/services and Quality Engineering and Continuous Improvement techniques, exercises judgment within defined procedures and policies to determine appropriate action, and frequently interacts with supervisors and functional peer groups to gain cooperation of others.

You're the right fit if:

• Bachelor’s degree in engineering disciplines or related field or a combination of equivalent job experience in related field.
• +5 year of experience in Quality or Manufacturing or other related fields
• Desirable ability to interpret technical drawings that may include mechanical dimensioning and Geometric Dimensioning and Tolerance (GD&T).
• Strong knowledge of Measurement and Test tools e.g. calipers, micrometers and methodologies for inspection (i.e. appropriately apply destructive and non-destructive testing) is preferred.
• 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, regression analysis, etc).
• Proven knowledge and application of applicable regulations for Medical Device manufacturing.
• 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.
• Intermediate level of English

How we work together

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.

Administrative role onsite;