Responsibilities

• Design, configuration, integration and implementation of process control solutions for the Life Sciences industry.
• Design, program, implement, test and document Emerson Delta V DCSs.
• Develop User Requirement Specifications.
• Develop Software and Hardware Design Specifications.
• Develop control system validation/testing protocols.
• Develop electrical panel schematics.
• Develop scope of supply documents.
• Manage automation projects as assigned.
• Monitor progress of projects.
• Install, test, and start-up control systems on-site.
• Work with plant engineers and operators to implement control strategies.
• Train operators and engineers on control systems.

Qualifications

• Requires a bachelor’s or master’s degree in mechanical engineering, Chemical Engineering, or related discipline degree is required
• Minimum of five (5) years’ experience in the biotech-pharmaceutical,
• Minimum of five (5) years’ experience in either a consulting engineering firm or operating engineering environment
• Experience in biotech/pharma industry is required
• Strong knowledge on review, understanding P&IDs drawings, ISA symbology is important
• Strong knowledge of automation narratives and architecture of DeltaV experience is a must
• Direct experience in the design/coding/qualification in any of the following systems: upstream / downstream bulk process equipment, lyophilization, formulation / fill vial and syringe forms, sterilization, Clean-In-Place, clean utilities (WFI/PW, Pure Steam, Clean Gases)
• Experience in commissioning and startup of control systems is required
• Experience with Visual Basic scripting
• Experience with PLC, HMI, and SCADA systems is a plus
• Experience with control system networking technologies and PC networking technology is a plus
• Experience working with SQL Server, Oracle, or other relational databases is a plus
• Specific knowledge of cGMPs and batch process control in the life science industry
• Knowledge of regulatory compliance inclusive of cGMP, 21 CFR Part 11 requirements, FDA regulations

Job Type: Full-time

Pay: $150,000.00 - $180,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Vision insurance

Schedule:

• 8 hour shift

Ability to commute/relocate:

• Orange, CA: Reliably commute or willing to relocate with an employer-provided relocation package (Required)

Experience:

• Biotechnology: 5 years (Required)
• Consulting: 5 years (Preferred)
• Delta V: 1 year (Required)

Work Location: In person

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