Job description
Company Overview LENSAR, Inc. is the leader in advanced robotic laser technology for refractive cataract surgery. LENSAR's laser systems offer cataract surgeons superior precision and accuracy, while optimizing overall visual outcomes. Our mission is to take the time to understand the needs of surgeons and their patients so that we can innovate our technology to ensure we meet their dynamic needs.
Interested in starting a career at LENSAR? As a global leader in next generation robotic laser for cataract surgery, our success depends on talented and motivated individuals who share our passion for making a difference in patients’ lives. We pride ourselves on having a highly collaborative, innovative environment where initiatives and teamwork are valued, and individual efforts are recognized.
Together we are one team one vision.
POSITION SUMMARY
Under the direction of the Manufacturing Supervisor or other qualified Operations staff, perform a wide variety of tasks and operations that are required to assemble and test Medical Device subassemblies in an FDA regulated manufacturing environment. Troubleshoot, maintain, and assemble all production equipment, as required.
Assist engineers on projects, repairs, and installations, as necessary. All operations will be carried out in compliance with GMPs, Standard Operating Procedures (SOPs), BOMs, and other LENSAR standards. In addition to performing the responsibilities/tasks below, the successful candidate will need to demonstrate the following traits: Passion and drive to develop and maintain a LEAN culture dedicated to providing the best results for our internal and external customers.
Continuously search for ways to improve/maintain the highest levels of productivity. Actively participate in a teamwork environment that maintains a high-performance culture.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Assemble and test components and subassemblies in compliance to set procedural guidelines, training, and timelines. Maintain (calibration & preventative maintenance) and assemble all production equipment and tooling, as required. Complete relevant paperwork following GMP guidelines and applicable training. Assist in developing methods and procedures to control, improve, or modify the manufacturing process.
Contribute to revisions of pertinent documentation, as appropriate. Prior to start-up, during processing, and at the completion of the manufacturing process, perform all documentation and clerical functions to provide the proper accountability and traceability of components and finished products. Perform cleaning/ housekeeping duties, as well as other collateral duties as assigned/required.
KNOWLEDGE / EXPERIENCE / SKILLS / EDUCATION To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
Required: Proficiency in the English language - reading, writing, and communication. Must be able to successfully pass all job-related tests and certifications required for working in a GMP, quality environment including but not limited to inspections and GMP requirements to perform essential functions of the job. Must re-qualify every year on all job-related tests and certifications as responsibilities or qualifications require.
High school diploma (or equivalent) and/or Associates Degree (or equivalent experience/coursework and technical knowledge, as assessed by the interviewing panel). Computer literate, including ability to interface with computer systems. Experience working with Microsoft suite (Word, Excel), navigating through web pages and e-mail.
Must possess basic typing skills. Ability to work overtime and travel as needed. Preferred: Ability to read and follow manufacturing work instructions and other product related documentation (schematics/mechanical drawings). Experience with test equipment such as Oscilloscopes, DVMs, curing systems, soldering tools, and basic hand tools.
Previous experience (including internships) in assembly of electro-mechanical equipment and/or equipment in a regulated environment. Target industries include DoD, pharmaceutical, biotechnology, biomedical, electronic, laser, and/or other medical industries. PHYSICAL DEMANDS These physical demands are representative of the physical requirements necessary for an employee to successfully perform the essential functions of the Manufacturing Technician
- Production’s duties. Reasonable accommodation can be made to enable people with disabilities to perform the described essential functions of the Manufacturing Technician
- Production’s duties and responsibilities. While performing the duties of this position, the employee is regularly required to communicate. The employee is frequently required to remain stationary. The employee is occasionally required to move about the facility. Occasionally, must be able to lift 45 pounds. WORK ENVIRONMENT Air-conditioned manufacturing environment, biological labs, clean room environments and dark rooms. In addition to a competitive salary, below are further benefits/rewards offered by LENSAR, Inc.: -Annual bonus opportunity -Company matched 401(k) plan with eligibility day one and immediate vesting -Employee Stock Purchase Plan (ESPP) and other company equity programs -Employer-sponsored comprehensive health plans- medical/dental/vision -Employer-paid disability insurance -Voluntary life insurance -Generous company holiday schedule -Paid time off program -Company-wide paid shutdown during the holidays
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