Manufacturing Engineer

Hi

If you are actively searching for new opportunities I would like to make you aware of Manufacturing Engineer Role. I will be happy to discuss what you may be looking for in your next role and what this position will offer your career.

Job Title: Manufacturing Engineer

Location: Seabrook NH 03874 (on site)
Job Type: 6 months Contract

Pay rate: $50/hr

H1B is fine

Client is looking for someone in NH or about 200 miles from NH (NJ NY CT MA NH RI ME etc)

About Our Client:
Our Client has been an ophthalmology instrumentmaker and 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 cuttingedge technology works closely with innovative surgeons and thrives to make a difference. Over 11000 ophthalmologists worldwide use their advanced Ophthalmic surgery unit to take care of their patients to help them see again.

Scope of Job
RCM is seeking an experienced Manufacturing Engineer to perform qualification and validation activities of manufacturing equipment and process. In addition the Engineer will work with manufacturing team to Develop process improvements generate new tooling and fixtures.

Primary Responsibilities

• Generate manufacturing documentation for new products. To include BOM routers drawing.
• Update current manufacturing work instructions drawings package labelling and test procedures.
• Develop process improvements generate new tooling and fixtures.
• Implement Lean improvements.
• Review and update technical files and design history files.
• Write review and sign all engineering documentation.
• Train manufacturing personnel as part of introducing new products/processes from the engineering phase to the production floor.
• Generate documentation and initiate validation of production methods.
• Assist in product registrations in foreign countries.
• Support manufacturing documentation and quality personnel in ISO 13485 GMP controlled environment.
• Analyze existing manufacturing processes identify and implement process improvements.
• Manage the Preventative Maintenance (PM) system.
• Troubleshooting and problem solving.

Qualifications

• Minimum of 5 years related experience. (Manufacturing Validation Process)
• Must have worked in a manufacturing environment with some experience with product and/or process development. Experience in writing IQ OQ PQ.
• A mechanical background is a plus.
• Auto Cad Solid Works ERP or MRP experience is also required.
• Medical device manufacturing experience is required.
• Design Transfer and plastic/molding experience is a plus.
• Must be proficient in using Microsoft Suite.