Senior R&D Technician
Apply now »Date: Mar 5, 2026
Location: Cartago, Costa Rica, CR, NA
Company: Heraeus
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About Heraeus
Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead.
About Heraeus Medevio
Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds.
To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today.
The Senior R&D Technician will play a key role in supporting process development and innovation
initiatives within the R&D department. This position is focused on bringing technical expertise and
hands-on support to the design, optimization, and transfer of manufacturing processes for medical
devices. The technician will act as a bridge between engineering and production teams, ensuring
processes are efficient, well-documented, and aligned with quality standards.
Essential Duties and Responsibilities
• 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.
Qualifications
• Associate’s or Technical Degree in Engineering, Manufacturing, or related field required;
Bachelor’s degree preferred.
• 5+ years of experience in medical device manufacturing, process development, or R&D
environment.
• Excellent bilingual (English/Spanish) verbal and writing communication skills.
• 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.
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