Sr. Automation Engineer – Drug Product Fill/Finish (Rockwell, PLC/DCS) JP14202
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 2, 2026
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Job Description:
Job Title: Sr. Automation Engineer – Drug Product Fill/Finish
(Rockwell, PLC/DCS) JP14202 Location: Thousand Oaks, CA. Employment
Type: Contract Business Unit: Advanced Technology & Automation
Duration: 3 years (with possible conversion to permanent) Posting
Date: 06/12/25 Pay Rate: $75 - $83/hour W2 Notes: Only qualified
candidates need apply. Fully on site in Thousand Oaks, CA. 91320.
8am-5pm M-F, OT possible 3 Key Consulting is hiring a Sr Engineer –
Automation Software (PLC, DCS, HMI, SCADA) for a consulting
engagement with our direct client, a leading global
biopharmaceutical company. Job Description: Sr. Engineer –
Automation Software will support manufacturing operations through
effective troubleshooting and ensuring automated equipment uptime
and reliability. Update and read piping and instrumentation
Diagrams (P&IDs), instrumentation and electrical design
packages including software design specs (SDS), hardware design
specs (HDS), user requirement specs (URS), qualification documents
(IQ, OQ, VP, VSR) among other engineering and validation
documentation. Development of detailed specifications, engineering
documents, SOPs and operating standards. Developing process control
applications utilizing Programmable Logic Controllers (PLC),
Distributed Control Systems (DCS), Human Machine Interfaces (HMI)
and Supervisory Control and Data Acquisition systems (SCADA).
Support projects focused on improving process
equipment/utilities/facilities -to- sophisticated unit operation
skids to integrate new drug product manufacturing technologies into
clinical/commercial facility. Familiarity with industry standards
for batch control systems, software development life cycle
methodologies, 21 CFR Part 11, and GAMP. Development of detailed
specification, engineering documents, SOP and computerized system
administration job plans. Testing of automation-based process
equipment. Ownership and administration of process control
automation in a GMP regulated manufacturing setting. Engage in
process change control requests per established SOP and processes.
Lead technical root cause analysis, incident investigations, and
troubleshooting on process control issues related to mechanical,
electrical, instrumentation and control systems. Support new
product introductions or new technology introductions by performing
engineering assessments, implementing automation system
configuration changes and supporting engineering runs. Devise new
approaches to complex problems through adaptations and
modifications of standard automation technical principles. Support
a safe working environment by complying with all pertinent
environmental health/safety practice, rules and regulations Why is
the Position Open? Additional work needed Top Must Have Skills: 5
years of experience working on Rockwell Automation and
Allen-Bradley PLCs (Factory Talk & ControlLogix). Experience with
Process Design, Commissioning and change control methodology.
Direct experience with regulated environments including detailed
understanding of cGMPs. Basic Qualifications: Doctorate degree OR -
Master’s degree & 2 years of directly related experience OR -
Bachelor’s degree & 4 years of directly related experience OR -
Associate’s degree & 8 years of directly related experience OR –
High school diploma / GED & 10 years of directly related experience
Preferred Qualifications: B.S or M.S. in Electrical Engineering,
Chemical Engineering, Mechanical Engineering, or Biotech
Engineering. Strong control system automation background focused
specifically in design, installation, programming and validation of
automated processes are essential. 5 or more years combined
experience with Rockwell Automation Factory Talk & ControlLogix PLC
Platform. Ability to create, update and read electrical design
packages including SDS, URS, IQ, OQ and VSR among other engineering
and validation documentation. Knowledge of S88 and S95 techniques.
- Batch processing a desired advantage. Strong leadership,
technical writing, and communication/presentation skills are
required. Work schedule flexibility as required to support 24/7
operations, requiring daily on-site and occasional after-hours
engineering coverage. Experience in developing automation
strategies for New Product Introduction and New Technology
Deployment. Preferred Experience using the following systems:
Lyophilizer System, Filling systems for Syringe and Vials and
Building Management System Testing and Inspection machines for
devices Clean Utilities (WFI Still A\B, Clean Steam Generator,
Chemical Dist. System, WFI Storage & Distribution and Purification
System) Cleaning Systems (Autoclaves, Depyro oven , COPs and Glass
Washers, Pressure Vessel Washer, Vial Washer and Ultrasonic Washer)
Position requires a working knowledge of building automation
systems, electronic batch records, PLC, OPC, Profibus, Ethernet/IP
and DeviceNet technologies. Working knowledge and experience with
cGMP procedures and engineering practices on pharmaceutical/biotech
production processes, facilities, and equipment. Candidate should
be experienced in change control, nonconformance, corrective and
preventative actions, and validation practices. Must be
independent, self-motivated, organized, able to multi-task in
project environments, and skilled in communication, facilitation,
and collaboration. Individual must be a team player prepared to
work in and embrace a team-based culture that relies on
collaboration for effective decision-making. Red Flags: Job hopping
- longevity concern Job is on-site. No remote work allowed.
Interview process: Phone screen followed by In-Person interview We
invite qualified candidates to send your resume to
resumes@3keyconsulting.com . If you decide that you’re not
interested in pursuing this particular position, please feel free
to take a look at the other positions on our website
www.3keyconsulting.com/careers. You are also welcome to share this
opportunity with anyone you think might be interested in applying
for this role. Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Lake Forest , Sr. Automation Engineer – Drug Product Fill/Finish (Rockwell, PLC/DCS) JP14202, Engineering , Thousand Oaks, California
