Manufacturing Contractor I

Summary:
As a Manufacturing Engineer Contractor, you’ll be at the forefront of ensuring top-notch quality and efficiency for automated and semi-automated production processes. This role focuses on the validation (IQ/OQ/PQ) of production equipment and processes, with a commitment to patient safety and product quality.

Key Responsibilities:

• Lead & Execute validation activities (IQ/OQ/PQ) for both automated and semi-automated equipment, ensuring new or revised production systems meet rigorous standards.
• Innovate & Implement manufacturing processes for ophthalmic medical devices used in essential eye surgeries.
• Optimize Production by applying Lean and Six Sigma techniques to streamline processes and improve quality.
• Ensure Process Stability through Continuous Monitoring and Statistical Process Control (SPC), keeping equipment...

BioPharma Consulting JAD Group is looking for a dedicated Manufacturing Contractor I to join our team. The Manufacturing Contractor I will perform routine clinical manufacturing operations at Alnylam’s Norton Manufacturing Facility under direct supervision. This position is responsible for ensuring safe, efficient, and cGMP-compliant operations at all times. Key duties include operating production equipment, executing standard procedures, and collaborating with support teams to maintain seamless production flow.

Responsibilities:

• Operate production equipment according to Standard Operating Procedures (SOPs) in the areas of weigh/dispense, solution preparation, equipment Cleaning in Place (CIP) and Cleaning Out of Place (COP), and small parts cleaning.
• Stock and manage materials in manufacturing suites to ensure readiness for production.
• Collaborate with support teams (Facilities, Quality Control, Quality Assurance, Materials...

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.
...

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...