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Stryker

Staff Manufacturing Engineer (Grecia, Manufacturing Site)

Grecia, Costa Rica

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hirly's read of this role

Seniority
Lead / management
Country
CR
Work mode
On-site / unstated
First seen by hirly
24 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Work Flexibility: Onsite

Join a team focused on bringing new manufacturing capabilities to Costa Rica through the transfer of a product from an international site. In this role, you will support manufacturing process transfer, validation, production readiness, and ongoing process improvement activities while working in a highly regulated medical device environment. This position offers the opportunity to collaborate with global teams and support the successful launch of new manufacturing lines.

What You Will Do

  • Lead manufacturing process transfer activities from international sites into production.
  • Develop and execute process, equipment, and packaging validation protocols in compliance with quality and regulatory requirements.
  • Analyze manufacturing performance data and implement process improvements to enhance quality, efficiency, and reliability.
  • Support manufacturing builds and production readiness activities for new product launches.
  • Investigate production issues and implement corrective actions using structured problem-solving methodologies.
  • Collaborate with cross-functional teams including Quality, Operations, Supply Chain, and Research & Development to support project objectives.
  • Create and maintain technical documentation including process reports, risk assessments, drawings, and validation records.
  • Train manufacturing personnel on new and existing processes and provide technical support to sustain production operations.

What You Will Need

Required Qualifications

  • Bachelor’s degree in Engineering or a related technical field.
  • Minimum 5 years of medical device manufacturing experience.
  • Experience supporting medical device process transfer projects.
  • Experience with manufacturing validations and process qualification activities.
  • Experience working with ISO requirements, FDA regulations, and design control processes.
  • Advanced English proficiency, written and verbal.
  • Valid passport and eligibility to travel internationally.

Preferred Qualifications

  • Experience with manufacturing process scale-up and new product introduction activities.
  • Experience using SAP or similar enterprise resource planning systems.

Travel Percentage: 20%

Original posting on Stryker's site ↗

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