Collabera is hiring: Manufacturing Engineer in Littleton

Weare based out of Morristown, NJ and we have been providing contingent labor to our clients for last 25 years. In 2015 we placed more than 6,000 contractors across select 100+ clients that we service. End client for this project is a large legal organizationwith operations in more than 100 countries and has more than 50,000 employees around the world. For eight consecutive years, Fortune has named this company as World’s ‘Most Admired Companies to work for’.

Responsibilities

• Maintains and improves procedures, documentation, tools, fixtures, and programs on existing printed circuit boards, electro-mechanical assemblies, and final products.
• Identify the root cause of manufacturing process and product nonconformities. Identify and implement the necessary actions to correct and prevent recurrence though the corrective and preventative action process.
• Participates with Product Development engineering in the creation/modifying of test programs to verify the performance to specification of new assemblies, peripherals, and products.
• Responsible for the maintenance of production test programs upon release to production.
• Responsible for diagnosing and investigating technical problems and resolving problems or developing solutions. Work in conjunction with other departments where appropriate.
• Generate and execute Process Validation protocols and continuously improve manufacturing documentation.
• Trains technicians on production methods, equipment, and procedures for new and existing assemblies and products.
• Improve Operations Quality System Processes to meet local and Corporate Quality initiative goals.

Qualifications

• Education Required: B.A./B.S. in Electrical Engineering, Manufacturing Engineering, Industrial Engineering or BioMedical Engineering.
• Years Of Experience: 2+ years of experience in a manufacturing support role
• Specialized Knowledge Required: Statistical knowledge; DOE, SPC, etc.; Ability to read and work with technical drawings and/or electrical schematics; Experience in Windows applications including Microsoft Office; Experience in FDA 21 CFR Part 820 Medical Device Manufacturing.

Preferred Qualifications

• Master’s Degree preferred.
• Familiar with the FDA’s Design Control process, and ISO requirements.
• Experience in automated testing using LabView, Test Stand or similar software.
• Knowledge of x-ray equipment and/or other capital equipment.
• Familiarity with Lean Manufacturing, and Six Sigma.

Additional Information

If interested and want to apply, please contact: