What are the responsibilities and job description for the Sr. R&D Engineer position at SARACA?
Job Functions:
· Independently lead R&D projects with customers, managing timelines, budgets, and quality deliverables.
· Develop new medical device products, conduct testing, analyze results, and optimize designs to meet performance requirements
· Prepare and maintain comprehensive technical documentation to support product development and regulatory submissions
· Actively contribute to the implementation of new ideas and concepts, enhancing product performance and quality
· Collaborate with cross-functional teams, including Production and Engineering, to ensure development processes align with industry best practices.
· Support compliance with medical device regulations and standards in close partnership with Quality and Regulatory teams
· Drive innovation and continuous improvement across products, processes, and methodologies
Skills:
· Knowledge of regulatory frameworks and quality standards (ISO, FDA, MDR)
· Microsoft Office Suite proficiency
· Excellent communication and leadership skills; proven ability to collaborate across teams and sites.
Experience:
· 3-5 years’ experience in developing MedTech products (implants, instruments, etc.) ideally within Sports Medicine, Orthopedics, or Spine.
· Prior experience working in a medical device company strongly preferred.
· Demonstrated project management expertise, successfully leading R&D initiatives
Education:
- · Bachelor’s degree in mechanical engineering, biomedical engineering or a related technical field.