Automation Engineer Senior, Software, Biotech DeltaV, SCADA, PLC - (JP5947)
Automation Engineer Senior, Software, Biotech DeltaV, SCADA, PLC - (JP5947)
Posted on :
30-05-2025
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1 Vacancy
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Hourly Salary
$ 72 - 82
Vacancy
1 Vacancy
Posted on :
30-05-2025
Job Description
Job Title:Automation Engineer Senior Software Biotech DeltaV SCADA PLC - (JP5947)
Location:Thousand Oaks CA.
Employment Type: Contract
Business Unit:Advanced Technology and Automation
Duration:3 years (with likely extensions and/or conversion to permanent)
Posting Date:05/27/24
Pay Rate:$72 - $82/hour W2 with benefits
3 Key Consulting is hiring a Senior Engineerfor a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Responsibilities:
Supplement additional workload on team.
Top Must Have Skills:
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:
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 sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
Location:Thousand Oaks CA.
Employment Type: Contract
Business Unit:Advanced Technology and Automation
Duration:3 years (with likely extensions and/or conversion to permanent)
Posting Date:05/27/24
Pay Rate:$72 - $82/hour W2 with benefits
3 Key Consulting is hiring a Senior Engineerfor 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
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 AB 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 sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
Regards
3KC Talent Acquisition Team
Employment Type
Hourly
Key Skills
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