Manufacturing Engineer II at RxSight, Inc.

Aliso Viejo, California, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Mar, 26

Salary

0.0

Posted On

19 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Manufacturing Processes, Continuous Improvement, Troubleshooting, Validation Strategies, ISO 13485, Lean Manufacturing, SolidWorks, Good Manufacturing Practices, Electrical Issues, Mechanical Issues, Root Cause Analysis, Training, Technical Support, Organizational Skills, Communication Skills, Self-Motivated

Industry

Medical Equipment Manufacturing

Description

Description RxSight® is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world’s first and only adjustable intraocular lens (IOL) that is customized after cataract surgery. The company’s mission is to revolutionize the premium cataract surgery experience by allowing surgeons to partner with their patients to achieve optimized results for every unique eye. OVERVIEW: The Manufacturing Engineer II will play a vital role in supporting and leading the sustaining efforts aimed at continuous improvement and maintaining robust manufacturing processes related to the Light Adjustable Lens and Insertion device manufacturing. As a vital member of the Manufacturing Engineering team, this individual will closely collaborate with Design Engineering and Quality Control/Assurance departments to ensure production line sustainability, compliance with regulations, and quality systems requirements. The Manufacturing Engineer II will be responsible for supporting lean manufacturing methodology and implementing the culture of continuous improvement to improve overall safety, quality, on-time delivery, and productivity of our LAL and Insertion device manufacturing and processes. This individual will also support the engineering team and other departments in identifying and resolving manufacturing processes and production issues. Requirements ESSENTIAL DUTIES AND RESPONSIBILITIES: Lead effort in support of continuous improvement initiatives aimed at enhancing production efficiency, ensuring business continuity, and maintaining regulatory compliance. Provide troubleshooting expertise for equipment-related issues and offer technical support to operators and technicians as required. Establish and execute validation strategies (IQ/OQ/PQ) for new processes, and equipment in compliance with ISO 13485 and FDA regulations. Initiate documents such as drawings, work instructions, and reports ensuring proper routing through the quality management system. Perform training necessary for the implementation of processes/tooling changes as necessary. Set up, operate, and maintain various manufacturing equipment and tools. Perform diagnostics, troubleshoot, and repair complex electrical, mechanical, network and software issues. Participate in root cause analysis and implement corrective actions for manufacturing issues. Ability to stay on tasks with minimal supervision and minimal direction. REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES: Demonstrates a hands-on approach to problem solving, ensuring prompt task closure. Familiarity with SolidWorks PDM software (desired). Proficient in conducting training sessions and initiating engineering change requests. Prior experience working in a cleanroom environment/ or medical device manufacturing is highly preferred. Professional, responsible, energetic, and accountable. Strong interpersonal skills – the ability to communicate effectively at multiple organizational levels including technicians, Engineering, Chemistry, and Production operators. Clear communicator – understands how to distill information to have substantive discussions with the right audience. Strong Organizational skills – the ability to balance and prioritize multiple studies, and manufacturing builds. Continued appetite to learn about our technology, its performance characteristics, and its manufacturing process – our process and our technology are unique! Self-motivated, proactive, and able to work effectively under minimal supervision. SUPERVISORY RESPONSIBILITIES: None EDUCATION, EXPERIENCE, and TRAINING: Bachelor’s degree in Biomedical, Electrical, or Mechanical Engineering with a minimum of 3 years of technical experience. Master’s degree in Biomedical, Electrical, or Mechanical Engineering with a minimum of 2 years of technical experience. Continuous improvement experience. Familiarity with regulatory standards (ISO 13485). Familiarity with good manufacturing practices (GMP) and good documentation practices (GDP). Experience with good laboratory practices (GLP) is a plus. CERTIFICATES, LICENSES, REGISTRATIONS: None COMPUTER SKILLS: Microsoft Word; Microsoft Excel; MiniTab CAD (SolidWorks or PRO/E proficiency preferred) Project Management System (SmartSheet preferred) Notice to Staffing Agencies and Search Firms: RxSight does not accept unsolicited resumes or candidate submissions from staffing agencies or search firms for any employment opportunities. All agency engagements must be authorized in writing for a specific position by RxSight’s Talent Acquisition department. Any resumes or candidate information submitted without such specific engagement will be considered unsolicited and the property of RxSight. No fees will be paid in the event a candidate is hired under these circumstances.

Responsibilities

The Manufacturing Engineer II will support and lead continuous improvement efforts in manufacturing processes for the Light Adjustable Lens and Insertion device. This role involves collaboration with various departments to ensure compliance, quality, and efficiency in production.