Job Details
DeltaV Automation Engineer
Location: Orange County/San Diego County
Experience: 5 years of experience
For over 25 years, the Life Sciences division of Trinity Consultants has supported clients in the pharmaceutical, biotechnology, and medical device industry. Comprised of Safe Bridge Consultants, ADVENT Engineering, and Aztec Technologies, Trinity s Life Sciences consulting team is a well-known leader in the industry.
Our Life Sciences consulting team focuses on providing highly technical expertise in Engineering, Validation, Automation, Compliance, and Safety (EHS) to our clients. You will have the opportunity to work with a variety of Subject Matter Experts (SMEs) on a diverse range of projects and technologies. With our commitment to client satisfaction and our global team of experienced professionals, Trinity s Life Sciences Division offers an exciting and rewarding career opportunity for individuals passionate about making a positive impact on patients lives and public health across the globe.
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.