Automation Senior Software Engineer, Biotech, DSC, SCADA HMI, PLC - (JP14368)
Company: 3 Key Consulting
Location: West Hills
Posted on: April 1, 2026
|
|
|
Job Description:
Job Title: Automation Senior Software Engineer, Biotech, DSC,
SCADA HMI, PLC - (JP14368) Location: Thousand Oaks, CA. Employment
Type: Contract Business Unit: Advanced Technology and Automation
Duration: 3 years with possible conversion to permanent Posting
Date: 08/04/2025 Pay Rate: $60 - $80/hour W2 DOE with benefits Note
: Fully onsite thousand oaks 8am-5pm M-F, OT possible 3 Key
Consulting is hiring a Senior Engineer for a consulting engagement
with our direct client, a leading global biopharmaceutical company.
Job Responsibilities: 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? Supplement additional workload on team. 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. Day to Day Responsibilities: Able to
support manufacturing operations through effective troubleshooting
and ensuring automated equipment uptime and reliability. Update and
read P&IDs, instrumentation and electrical design packages
including SDS, HDS, URS, IQ, OQ, VP and VSR among other engineering
and validation documentation. Development of detailed
specification, engineering documents, SOP and operating standards.
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: a.
Lyophilizer System, Filling systems for Syringe and Vials and
Building Management System b. Testing and Inspection machines for
devices c. Clean Utilities (WFI Still A\B, Clean Steam Generator,
Chemical Dist. System, WFI Storage & Distribution and Purification
System) d. Cleaning Systems (Autoclaves, Depyro oven , COPs and
Glass Washers, Pressure Vessel Washer, Vial Washer and Ultrasonic
Washer) 10) 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. Employee Value
Proposition: Great company culture, beautiful campus, and chance to
work with innovative technology. Red Flags: Job hopping - longevity
concern Job is on-site. No remote work allowed. Interview process:
Two-step 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, Ventura , Automation Senior Software Engineer, Biotech, DSC, SCADA HMI, PLC - (JP14368), Engineering , West Hills, California
