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Senior R&D Technician
Minor Hotels Europe and AmericasSenior R&D Technician involved in process development and optimization for medical devices. Collaborating with engineers to enhance manufacturing processes and quality standards in Costa Rica.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in process development, validation, and optimization within medical device manufacturing, utilizing lean and Six Sigma principles to enhance product quality and efficiency. Proficient in technical documentation, equipment setup, and cross-functional collaboration to support new product introductions.
Highest-signal resume keywords
Process DevelopmentLean PrinciplesSix Sigma MethodologiesTechnical DocumentationMedical Device Manufacturing
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Process ValidationEquipment TroubleshootingInspection Equipment ProficiencyEngineering Drawing InterpretationMeasurement Tools Usage
Soft Skills
Effective CommunicationCollaboration SkillsProblem-Solving SkillsMentorship AbilitiesAdaptability
Tools & Technologies
Microsoft OfficeSAPVision SystemsMicrometersCalipers
Industry Keywords
Good Documentation PracticesClean Room EnvironmentsPilot ProductionR&D EnvironmentProduct Transfers
About the role
Key responsibilities & impact- Support the development, optimization, and validation of processes, tooling, and equipment for new product introductions
- Perform advanced equipment setup, troubleshooting, and maintenance to ensure reliability during process development
- Execute complex product builds across all development phases, including feasibility, characterization, and validation
- Collect, analyze, and report process data to support decision-making and continuous improvement initiatives
- Collaborate with engineers to design and implement fixtures, tooling, and process improvements
- Provide mentorship and training to junior technicians and operators, promoting best practices and adherence to procedures
- Serve as the primary technical point of contact for pilot production and early-stage product transfers
- Participate in cross-functional reviews and contribute technical input to project documentation
- Apply lean and Six Sigma principles to streamline processes, reduce waste, and enhance product quality
- Ensure compliance with Good Documentation Practices, safety standards, and company policies
Requirements
What you’ll need- Associate’s or Technical Degree in Engineering, Manufacturing, or related field
- 5+ years of experience in medical device manufacturing, process development, or R&D environment
- Strong ability to read and interpret engineering drawings, technical documents, and validation protocols
- Proficient in the use of inspection equipment and measurement tools (vision systems, micrometers, calipers, etc.)
- Hands-on experience with process validation, documentation, and transfer to production
- Strong troubleshooting and problem-solving skills, with the ability to work independently and in teams
- Proficient in Microsoft Office tools (Word, Excel, PowerPoint) and experience with SAP or similar systems
- Effective communication and collaboration skills across multiple functions and levels of the organization
- Adaptability to dynamic work environments such as clean rooms, labs, and pilot production areas
Benefits
Comp & perks- Health insurance
- Retirement plans
- Flexible work arrangements
- Professional development