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Principal Automation Engineer; Delta V​/Emerson​/DCS Thousand Oaks, CA

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Infotree Global Solutions
Full Time position
Listed on 2025-12-23
Job specializations:
  • Engineering
    Biomedical Engineer, Electrical Engineering, Quality Engineering, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 200000 - 250000 USD Yearly USD 200000.00 250000.00 YEAR
Job Description & How to Apply Below
Position: Principal Automation Engineer (Delta V /Emerson/DCS) at Infotree Global Solutions Thousand Oaks, CA

Principal Automation Engineer (Delta V / Emerson / DCS) – Infotree Global Solutions, Thousand Oaks, CA Description

  • Principal Automation Engineer (Delta V)

    The ideal candidate for the Principal Automation Engineer (Delta V) role will have extensive expertise in Delta V batch control systems, with a minimum of 4–5 years of direct, hands‑on Delta V experience specifically in pharmaceutical manufacturing environments. They should demonstrate proficiency in coding, troubleshooting, and addressing complex alarms or system issues in Delta V. Candidates should ideally hold a Bachelor’s degree (Chemical, Electrical, Automation Engineering, Computer Science, Electronics, or similar technical field).

    However, substantial practical Delta V experience can outweigh formal educational qualifications. A strategic mindset, excellent troubleshooting skills, and strong interpersonal capabilities are crucial, as the role involves frequent collaboration across various teams. Experience in PLC systems and Delta V system administration is beneficial but not mandatory. Candidates must show a track record of stability in their previous employment, with demonstrated capacity for maintaining long‑term roles.

  • Lead Principal Engineer for Medical Devices

    Lead teams in the development of drug delivery devices. Scope includes a wide range of devices, such as needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro‑infuser delivery pump systems. The qualified candidate will lead technical teams to ensure successful device development of these mechanical and electro‑mechanical medical devices. The Principal Engineer will work closely with team members to develop detailed engineering specifications, device design & development, support verification, validation, and regulatory submissions of these devices.

    The role of the Principal Engineer is to work within a cross‑functional organization to utilize technologies and methodologies that support short‑cycle robust device development.

    Responsibilities
    • Work cross‑functionally with individuals and project teams in Marketing, Operations, and Development
    • Create and assess product requirements to determine technical coverage and proper integration of different subsystems
    • Create and execute project plans and schedules
    • Develop, execute, and review architecture documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects
    • Provide deep technical assistance for junior engineers
    Skills
    • BS in Engineering and previous experience in a medical device industry
    • 10 years current experience with engineering processes and procedures
    • Led projects from development through the 510(k) and PMA approval process
    • Strong background in engineering and commercialization of electro‑mechanical medical devices
    • Experience with material & test specs generation, protocol & report writing, process & test development, prototyping, design verification, DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA
    • Product design/development (design control) from concept to post‑product launch for Europe (EMEA/CE Mark) & US (FDA/PMA/510(k)) submissions
    • Experience in drug/device combination product design and development
    • Familiar with the following standards:
      • Quality System Regulation (21 CFR 820)
      • Risk Management (ISO 14971)
      • EU Medical Device requirements (Council Directive 93/42/EEC)
      • Medical Electrical Equipment (EN 60601)
    • Small‑scale device assembly experience
    • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations
    • Strong problem‑solving, risk assessment, and risk management skills
    • Must be capable of working on multiple projects in a deadline‑driven environment
    • Very important note:
      Qualified candidates with either a strong Electrical Engineering, Mechanical Engineering, or Systems/Software Engineering background need apply and will be considered!!!
Top 3 Must Have Skill Sets
  • Emerson Delta‑V DCS system with batch control and recipe management
  • System Integration using OPC, Profibus, EIP, WIOC,…
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