| Sr. Validation Engineer at Remote, Remote, USA |
| Email: [email protected] |
| From: Ryan, nitya software [email protected] Reply to: [email protected] Role: Manufacturing Engineer (Medical devices) Location: Its an onsite position in Seabrook, NH 03874 6 months Plus Contract position OR Right to Hire Interview: First round MS Team Video, Final Round- in person at Seabrook, NH. Job Function: Qualify and Validate Software and Equipment in Manufacturing About Our Client: Our Client has been an ophthalmology instrument-maker to global market leader for 35 years! Every single day their 500 enthusiastic employees ensure that eye surgeons all over the world enjoy the use of innovative ophthalmic devices, instruments, and liquids. Our Client uses cutting-edge technology, works closely with innovative surgeons, and thrives to make a difference. Over 11,000 ophthalmologists worldwide use our advanced Ophthalmic surgery unit EVA to take care of their patients to help them see again. Scope of Job: The client is going through a tech transfer from another facility. We are seeking a Sr. Validation Engineer to support the qualification and validation of the equipment in the target facility. Primary Responsibilities: Understand client methods and procedures Using client templates and protocols Develop protocols to qualify and validate related software components. Work with QA to obtain review and approvals of work package Support execution of test script and develop Summary Reports Other duties as necessary Qualifications: Must have a four-year degree in a technical area, Minimum of 5 years related experience. Medical device protocol and validation experience & proficiency is a must. Be highly reliable and onsite with minimal remote work. Great communicator and team player collaborates well with various depts Documentation proficiency (Protocol & Validation reports, mfg procedures, drawings) Must have worked in a manufacturing environment with some experience with product and/or process development. A mechanical background is a plus. Medical device manufacturing experience desired. Design Transfer and plastic/molding experience is a plus. Must be proficient in using Microsoft Suite. Required Education & Experience Bachelor's Degree in Technical Field Minimum of 5 years related experience. Equal Employment Opportunity Statement Our Client provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. Keywords: quality analyst information technology microsoft New Hampshire |
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| Fri Nov 24 20:24:00 UTC 2023 |