Company:
STAAR Surgical
Location: Tustin
Closing Date: 04/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
MAIN JOB RESPONSIBILITIES
- 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.
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STAAR Surgical
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