MAIN JOB RESPONSIBILITIES / COMPETENCIES
1.    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.
2.    Develops product specifications, manufacturing methods and procedures under supervision.
3.    Conducts test protocols, verification and validation activities, and equipment qualifications under supervision.
4.    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.
5.    Assists in product conceptualization and design and feasibility testing. Documents work in laboratory notebooks and Technical Reports.
6.    Other duties as assigned.

REQUIREMENTS

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.

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.

Pay range is $80K to $120K - Final compensation will be based on experience.