Senior Manufacturing Engineer

Minor Hotels Europe and Americas

Manufacturing Engineer executing engineering actions and ensuring production line compliance. Coordinating engineering processes and implementing continuous improvement projects in medical device production.

Posted 7/26/2026full-timeCartago • 🇨🇷 Costa RicaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in executing manufacturing engineering actions and continuous improvement projects within the medical industry, ensuring compliance with quality regulations and standards. Proficient in statistical techniques and methodologies such as Six Sigma and Lean to enhance production efficiency and reduce interruptions.

Highest-signal resume keywords

Manufacturing EngineeringContinuous Improvement ProjectsStatistical Techniques (DOE, SPC)Validation Medical Manufacturing ProcessISO13485 and FDA Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Electrical EngineeringMechatronicsRoot Cause InvestigationProblem Solving MethodologiesTransfer Process Projects ImplementationBudget ControlCost of Goods Sold (COGS)Lean MethodologySix Sigma MethodologyTechnical Support

Soft Skills

Organizational Environment PromotionCollaboration

Tools & Technologies

SAPMinitabAutoCADSolidWorks

Industry Keywords

Medical IndustryCatheter ExperienceQuality Compliance RegulationsManufacturing Production NeedsProduction Line Support

About the role

Key responsibilities & impact

Execute manufacturing engineering actions, projects and investigations assuring the sustaining of production lines according to quality compliance regulations
Coordinate the engineering process to allow the execution of priorities and projects according to manufacturing production needs
Coordinate with different areas (logistics, purchasing, planning and quality) assuring that production running without interruptions and products and processes improvements are in compliance with standards and quality system
Implement continuous improvement projects in products and processes to reduce the risks of interruptions in production or quality regulations
Keep a foster organizational environment to promote HMCR values and culture
Developed processes, documentation and records, after production release assuring the manufacturing and quality regulations
Execute manufacturing priorities and process according to the indicators of yield, quality, and cost, through methodologies (Six Sigma DMAIC, DOE’s, Lean) assuring the SPCs
Perform manufacturing technical support during the validation, and post-production to avoid line interruptions and high scrap

Requirements

What you’ll need

Electrical/Electronic Engineering; Mechatronics or related Bachelor´s Degree
Engineering Master’s degree in field related is desirable
5+ years in similar positions
4+ years of work experience in medical industry
Catheter experience preferred
Intermediate-Advanced in spoken and written business English
Transfer Process Projects implementation experience
Experience supporting production lines and leading root cause investigations used problem solving methodologies
Continuous improvement projects implementation experience
Validation medical manufacturing process experience
Statistical techniques knowledge (DOE, SPC, etc.) is required plus experience with continuous improvement methodologies
Proficient in using SAP is desirable
Normative ISO13485 and FDA
Lean and six sigma knowledge
Knowledge in CAPEX, Budget control and COGS
Software: Minitab
Software: AutoCad & Solidworks are nice to have

Benefits

Comp & perks

Flexible working hours
Professional development opportunities