NPI Engineer II

Heraeus

NPI Engineer II executing product transfer projects and ensuring compliance at Heraeus Medevio in Costa Rica. Collaborating with teams to implement new products and processes with a focus on quality.

Posted 7/30/2026full-timeCartago • 🇨🇷 Costa RicaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in process validation, project implementation, and compliance within the medical manufacturing industry, with a strong focus on Lean methodologies and budget management. Proficient in training and developing teams to achieve high-quality performance and operational objectives.

Highest-signal resume keywords

Process ValidationLean MethodologiesCAPA KnowledgeSix Sigma Green BeltBudget Control

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Process ValidationBudget ControlCOGS ManagementLean ToolsDOE StudiesGage R&R StudiesTechnical DocumentationTransfer Process ImplementationContinuous Improvement ProjectsManufacturing Process Compliance

Soft Skills

Team DevelopmentTraining DeliveryCross-Functional Collaboration

Tools & Technologies

SAPMinitab

Certifications & Qualifications

Six Sigma Green Belt

Industry Keywords

Medical ManufacturingCAPAValidationScrap AnalysisDowntime AnalysisYield Analysis

About the role

Key responsibilities & impact

Execute implementation activities to support the transfer process at HMCR Costa Rica site by performing process validations (IQ’s, OQ’s and PQ’s), configuring SAP system data (routings, BOM’s and COGS), assisting with budget tracking and CAPEX requests, and running manufacturing and inspection processes in compliance with the quality system.
Coordinate with project manager to define transfer stages, timelines, resources, and customer requirements.
Prepare and update technical documentation to enable decisions and ensure compliance.
Track ramp-up performance by analyzing scrap, downtime, and yield using Lean tools.
Maintain COGS accuracy in SAP for new parts and report deviations.
Perform basic DOE and Gage R&R studies under Sr. Engineer guidance.
Deliver training sessions for operators and technical staff on new product requirements.
Contribute to CAPA, Complaint, and Nonconformance investigations by proposing corrective actions.
Align with other departments to ensure resources for validation, training, and compliance requirements are met.
Develop and support the technician team to consistently deliver high‑quality performance while coordinating daily operational activities that ensure successful execution of project and production objectives.
Participate in cross-functional teams for new products/processes, ensuring integration into manufacturing.

Requirements

What you’ll need

Bachelor’s degree with a major in Engineering fields (Electronic, Materials, Maintenance, Mechanical, Electric, Industrial, Production and others).
Validation medical manufacturing process experience.
Fluent in spoken and written business English.
Lean and six sigma knowledge.
Knowledge in CAPEX, Budget control and COGS.
CAPA knowledge.
Software: Minitab.
3-5 years of work experience in medical industry.
Transfer Process Projects implementation.
Continuous Improvement Projects implementation.
Six Sigma Green Belt.

Benefits

Comp & perks

Health insurance
Professional development opportunities