Manufacturing Engineering Tech TEMP

Job Description Dutch Ophthalmic USA and Peregrine Surgical are part of DORC, short for Dutch Ophthalmic Research Center, manufactures equipment, instruments and liquids used in eye surgery. DORC uses cutting-edge technology, works closely with innovative surgeons, and thrives to make a difference. Ophthalmologists worldwide use our advanced Ophthalmic surgery unit EVA to take care of their patients to help them see again. DORC is a ZEISS company, an internationally leading technology enterprise that develops, manufactures and sells highly innovative products and solutions in a variety of business fields, such as medical technology. As a company wholly owned by a foundation, ZEISS is rooted in and committed to responsibility in all its activities. The Manufacturing engineer is responsible for activities that include but are not limited to design, simulation, building, test and documentation to develop and/or maintain/ improve production tools and test equipment for the manufacturing of products for ophthalmic surgery. This also includes the development and improvement of production processes and related documentation. All activities need to be carried out in conformity with international regulations, safety and performance standards as applicable. Peregrine Surgical, LLC is part of the Dutch Ophthalmic Research Center - a Zeiss Company; Provide engineering support to all production sites within the US

• Update current manufacturing work instructions, drawings, package labeling, and test procedures.
• Develop process improvements, generate new tooling and fixtures
• Provide engineering support and expertise in the investigation of nonconformances and CAPA
• Analyze existing manufacturing processes, identify and implement process improvements.
• Manage the Preventative Maintenance (PM) system
• Process documentation and production documents (e.g. Process requirements, SOPS, maintenance plans)
• Analytically driven, solving (electro)mechanical machine problems
• Performing machine and process tests and analyzing process data (DOE)
• Preparing risk analyses of assembly and test processes (PFMEA)
• Training and supervising production personnel and final inspectors in production
• MSc. in mechatronics, mechanical engineering, product design,
• Preferred 1-5 years experience in medical device or other regulated industry.
• Regulations and standards in Medical Devices (e.g. Standard IT skills (Office, Outlook etc.)
• Experience with 2D and 3D CAD (ideally AutoCAD and Solid Works)
• Process data analysis and specific software (e.g. Knowledge of production techniques and market available solutions and technologies as well as certification requirements of manufacturing equipment
• Risk management principles, Process FMEA
• English: full professional proficiency
• 10 US holidays
• 90% of Health Insurance premiums paid by the company.
• Dental & Vision coverage
• Paid short term, long term & basic life insurance paid by the company.
• Bonus program