To Discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL www.linkedin.com/in/deepakarya8a79aa22a/), email your updated resume at Email deepak.arya@collabera.com. Thank you!

Pay Range: $18 to $23 an hour.

Client Industry: Medical Device

Job Mode: Onsite

Contract Duration: 10 - 12 Weeks

Job Summary:

The Facilities Engineering Co op will support engineering, manufacturing, and facilities operations within a regulated production environment. This position provides hands on experience with automation systems, equipment maintenance, validation activities, and process improvement initiatives. The candidate will collaborate with engineering, maintenance, quality, and production teams to improve operational efficiency and ensure compliance with quality standards. This opportunity is ideal for engineering students seeking exposure to medical device and manufacturing environments. The role also includes involvement in facility upgrades, technical documentation, and Lean manufacturing projects.

Key Responsibilities:

• Support facilities technicians and engineering teams across manufacturing operations
• Run and monitor automation systems and support troubleshooting activities
• Create and revise SOPs, training materials, and technical documentation
• Train personnel on updated procedures and operational processes
• Drive compliance with approved operational and quality procedures
• Assist with equipment and process validation activities
• Support facility construction and room build out projects
• Develop and update piping and instrumentation diagrams
• Communicate operational issues and escalate concerns to appropriate teams
• Participate in Lean manufacturing and continuous improvement initiatives

Required Qualifications:

• Currently pursuing a BS or MS degree in Mechanical Engineering, Electrical Engineering, Chemical Engineering, Biochemical Engineering, or Biomedical Engineering
• Ability to follow written and verbal instructions
• Strong communication and documentation skills
• Knowledge of manufacturing environments and process improvement concepts
• Ability to support troubleshooting and operational activities

Preferred Qualifications:

• Experience working in GMP or ISO regulated environments
• Knowledge of cGMP and ISO 13485 standards
• Exposure to manufacturing, engineering, maintenance, or facilities operations
• Experience with validation activities and automation systems
• Understanding of clean room or medical device manufacturing environments

Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, longterm disability insurance, shortterm disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually AS Applicable)