Performs activities associated with the development of new ophthalmic lenses and delivery systems and supports existing products and processes in accordance with Design Control procedures.
Develops product specifications, manufacturing methods and procedures under supervision.
Conducts test protocols, verification and validation activities, and equipment qualifications under supervision.
Prepares test protocols and reports, verification and validation reports, and equipment qualification protocols under supervision. Responsible for producing product development documentation in accordance with Good Documentation Practice.
Assists in product conceptualization and design and feasibility testing. Documents work in laboratory notebooks and Technical Reports.
Other duties as assigned.
EDUCATION & TRAINING
B.S. in Engineering or Science discipline. Master's degree preferred but equivalent combination of education/experience acceptable.
EXPERIENCE
Minimum 2 years industry experience or equivalent.
Minimum 1 year in medical device industry.
Knowledge of Design Control procedures and Quality systems.
Experience developing and transferring new products.
Image processing experience helpful.
SKILLS
Good analytical and problem-solving skills.
Knowledge of and ability to follow Design Control requirements.
Knowledge of validation and verification techniques.
Self-starter and works well with others.
Good communication and organizational skills.
Working knowledge of Solid Works, CAD or AUTOCAD preferred.
Independent thinking in order to solve engineering problems.
STAAR Surgical is an equal employment opportunity employer.