Manufacturing Engineer Contractor

Our client in Houston, Texas is seeking 3 Manufacturing Engineer Contractors. The contractors will be responsible for leading, executing, documenting, and managing validation activities (IQ/OQ/PQ) necessary to support the introduction or revision of automated and semi-automated production equipment and processes for ophthalmic medical devices.

Key Responsibilities:

• Lead, execute, document, and manage validation activities (IQ/OQ/PQ) for automated and semi-automated production equipment and processes.
• Design, develop, validate, and implement manufacturing processes for building ophthalmic medical devices for cataract and vitreoretinal surgeries.
• Support production process optimization through Lean and Six Sigma methodologies.
• Apply concepts of Continuous Monitoring through Statistical Process Control (SPC) to ensure processes are monitored and controlled appropriately, maintaining equipment in a validated state.
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Our client in Houston, Texas is seeking 2 Manufacturing Engineer Contractors. The contractors will be responsible for leading, executing, documenting, and managing validation activities (IQ/OQ/PQ) necessary to support the introduction or revision of automated and semi-automated production equipment and processes for ophthalmic medical devices.

Key Responsibilities:

• Lead, execute, document, and manage validation activities (IQ/OQ/PQ) for automated and semi-automated production equipment and processes.
• Design, develop, validate, and implement manufacturing processes for building ophthalmic medical devices for cataract and vitreoretinal surgeries.
• Support production process optimization through Lean and Six Sigma methodologies.
• Apply concepts of Continuous Monitoring through Statistical Process Control (SPC) to ensure processes are monitored and controlled appropriately, maintaining equipment in a validated state.
...

BioPharma Consulting JAD Group has a great Contract Medical Device Manufacturing Engineer role with an industry leader in Houston, TX. This is a temporary position with the possibility of extension.

The candidate will work in a highly collaborative team environment, you will play a crucial role in ensuring the efficient and effective production of ophthalmic medical devices. Your responsibilities will span various stages of the manufacturing process, from validation to continuous improvement. Here’s what you’ll be doing:

Job Responsibilities:

• Lead, execute, document & manage the validation activities (IQ/OQ/PQ) necessary to support the introduction or revision of automated and semi-automated production equipment and processes for Ophthalmic medical devices.

• Design, develop, validate and implement manufacturing processes to build ophthalmic medical devices for cataract and vitreoretinal...