Senior Automation Engineer

Discover International; Thousand Oaks (CA); On-site; USD 55,000 - 140,000; Full time

Job summary

Discover International is seeking an Automation Engineer for a 3-year contract in Thousand Oaks, CA. The position requires a background in Delta-V and PLC with responsibilities ranging from leading automation projects to ensuring GMP compliance. Ideal candidates will have substantial experience in regulated life sciences and strong technical skills, offering an exciting opportunity in a leading biotech firm.

Qualifications

• 5+ years of automation experience in GMP-regulated life science facilities.
• Hands-on with DeltaV DCS, Rockwell PLCs, electronic batch systems.
• Knowledge of regulatory frameworks like 21 CFR Part 11.

Responsibilities

• Lead automation scope for capital projects from planning through post-implementation.
• Collaborate with various teams for integrating systems and ensuring adherence to standards.
• Train end-users and manage documentation.

Skills

Delta-V

PLC

System integration

Regulatory compliance

Project management

Cross-functional communication

Education

Bachelor's in Electrical/Computer Science, Chemical, Biotech Engineering or related

Job description

Direct message the job poster from Discover International

Lead Account Manager, Contracts @ Discover International

Automation Engineer - 3 year contract!

Onsite - Thousand Oaks, CA

I'm partnered with a leading biotech that is seeking an experienced Automation Engineer with a strong background in Delta-V & PLC!

Key Responsibilities:

• Lead automation scope for capital projects from planning through post-implementation.
• Represent the Plant Automation team across project phases: design, execution, and validation.
• Collaborate with Engineering, Manufacturing, GCPM, and IT to integrate systems like:
• Rockwell SCADA and PLCs
• HMI/SCADA infrastructure
• Ensure adherence to standards, GMP compliance (21 CFR Part 11), and engineering protocols.
• Train end-users, revise SOPs, manage CMMS systems, and deliver support documentation.
• Support both new technology introductions and day-to-day drug substance operations.

Qualifications:

• Bachelor’s in Electrical/Computer Science, Chemical, Biotech Engineering, or related.
• 5+ years of automation experience in GMP-regulated life science facilities.
• Hands-on with DeltaV DCS, Rockwell PLCs, electronic batch systems, and SCADA architecture.
• Knowledge of system integration (OPC, Fieldbus, DeviceNet, etc.).
• Familiar with regulatory frameworks: 21 CFR Part 11, S88, S95, ASTM 2500, GAMP.

Preferred:

• Strong project management and cross-functional communication skills.
• Experience with capital project lifecycle, including validation and commissioning.
• Ability to lead, influence, and train stakeholders at all levels.
• Detail-oriented, self-motivated, and comfortable in fast-paced environments.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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