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Heraeus

Process Development Engineer II

Heraeus

Lead design and development activities for medical devices at Heraeus Medevio in Cartago. Oversee project execution, mentoring, and technical deliverables in engineering team.

Posted 7/31/2026full-timeCartago • 🇨🇷 Costa RicaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading design and development activities in the medical device industry, with a strong focus on engineering analysis, documentation practices, and effective communication in both Spanish and English. Proficient in making data-driven decisions using statistical tools and methodologies.

Highest-signal resume keywords
Bachelor's Degree In EngineeringSolid Works CertificationSix Sigma Green And/Or Black Belt CertificationISO 13485 Design Control KnowledgeStatistical Tools Proficiency

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Engineering AnalysisDesign VerificationTechnical WritingData Driven Decision MakingTolerance Stack-Up AnalysisDesign Control DocumentationProcess ValidationStatistical Process ControlDesign Execution PlanningDocumentation Practices
Soft Skills
Effective CommunicationMentoringFacilitationCollaborationCustomer Interaction
Tools & Technologies
MinitabStatistical ToolsDesign Software
Certifications & Qualifications
Solid Works CertificationSix Sigma Green BeltSix Sigma Black Belt
Industry Keywords
Medical Device IndustryISO 13485Design ControlProcess ValidationEngineering Functional Areas

About the role

Key responsibilities & impact
  • Lead design and development activities throughout the lifecycle of products.
  • Create technical execution plan and deliverables with the project manager.
  • Lead customer interaction on technical deliverables.
  • Mentor engineers on the team to conduct engineering analysis on designs.
  • Lead and monitor documentation practices for requirements, design output, and design verification.
  • Communicate complex information concisely and clearly to all levels of collaborators.
  • Facilitate and make technical decisions on projects.

Requirements

What you’ll need
  • Bachelor’s degree in Engineering or related technical field required.
  • Minimum of 5+ years of relevant work experience in medical device industry.
  • Solid Works certification.
  • Six Sigma Green and/or Black Belt certification.
  • Well established knowledge of multiple engineering functional areas.
  • Knowledge of ISO 13485 Design Control and Process Validation documentation required.
  • Highly effective communication and technical writing skills in Spanish and English.
  • Able to make data driven decisions utilizing statistical tools such as DOE, tolerance stack-up analysis, or Minitab.

Benefits

Comp & perks
  • Career growth opportunities
  • Training and development resources
  • Mentorship program
  • Engaging work environment