Design, development and prototyping of new products in accordance with company Product Development Process (PDD) requirements to meet functional, clinical, customer and manufacturing requirements.
Peer review and technical support to other engineers to improve the overall engineering ability and knowledge within the department and company.
Research and maintain a strong and current understanding of relevant new product development and manufacturing technologies and their application to medical device design to meet or exceed customer, company, and project needs
Evaluate and document the feasibility, reliability, and risk of concepts and / or prototypes through engineering testing and analysis in order to demonstrate that the product performance, manufacturability, safety and cost are consistent with the customer, regulatory and production requirements.
Develop timelines and cost estimates for development tasks and appraise management of performance against plan, communicating and reporting progress to project management to maintain and track compliance to project schedule.
Generate and review design history file documentation in compliance with GMP, QSR, ISO and company PDD requirements throughout the project life cycle to ensure the design is fully documented.
Coordinate vendor activities relative to communication of specifications, development schedules and progression tracking in order to obtain components, supplies or equipment to support prototype or product procurement and assembly.
The delivery of manufacturable designs acceptable to operations by applying Design for Manufacture principles and feedback from manufacturing engineers, external suppliers and other sources
Bachelor’s degree in Electronic Engineering or equivalent and minimum of six years of relevant engineering experience in high technology regulated industry.
Experience in development of real-time embedded systems
Detailed knowledge of up to date software development and test methods
Familiarity with software configuration management tools, design tools, and peer review
Ability to understand electronic circuit schematics.
Excellent written and oral team communication skills.
Competency in material processing technologies and wide range of part manufacturing methods.
Ideally GMP, ISO 13485, IEC62304, IEC60601 and QSR knowledge as practiced in the medical device industry
Standard competencies :
Consistently hold people to account by making expectations explicit and regularly reviewing performance
Motivate others through leading by example and creating an expectation that our colleagues do the same
Provide both timely positive and negative feedback
Understand our customers needs and deliver on our agreed commitments managing both risk and value to provide an optimum solution
Communicate clear goals, objectives, consequences and timeframes for everyone
Develop right first time approach to everything
Foster respect, openness, collaboration and trust
Empower and equip our people to take responsibility
Generous Pension Scheme
Free Life Assurance
Private Medical Insurance
33 Days holiday (inc Bank Holidays)
About Olympus Medical Systems
The Medical Systems Division represents Olympus’ largest business domain and is the global market and technology leader for medical endoscopes.
Olympus aims to continuously find better and more economical solutions to medical issues which improve the well-being of patients, enhance the working environment for doctors and nursing staff and help to develop the overall performance of health care providers.