Delta-V Automation Project Manager

Stark Pharma Solutions Inc; San Diego (CA); On-site; USD 120,000 - 150,000; Full time

Job summary

Stark Pharma Solutions Inc is seeking a Delta-V Automation Project Manager / Automation Engineer to lead automation projects onsite in San Diego, CA. The ideal candidate should hold a Bachelor's degree in Engineering and possess over 8 years of relevant experience, particularly in the pharmaceutical or life sciences industry.

This role involves managing automation projects from initiation through to operational readiness, ensuring adherence to industry compliance standards, and effectively collaborating with cross-functional teams.

Qualifications

• 8+ years of automation engineering or project management experience in relevant fields.
• Strong knowledge of PLC, DCS, SCADA, HMI, and industrial control systems.
• Experience with CSV, CQV, commissioning, and GMP compliance.

Responsibilities

• Lead automation projects from concept to operational readiness.
• Manage project scope, schedules, budgets, and vendor deliverables.
• Ensure compliance with cGMP, GAMP 5, and Data Integrity requirements.

Skills

Automation engineering

Project management

PLC and DCS knowledge

GMP compliance

Education

Bachelor's degree in Engineering

Tools

SCADA

HMI

CSV

Job description

Role: Delta-V Automation Project Manager / Automation Engineer (Life Sciences)

Location: San Diego, CA - Onsite

Duration: Long-Term Contract

Responsibilities

• Lead automation projects from concept through design, implementation, commissioning, qualification, and operational readiness.
• Manage project scope, schedules, budgets, risks, and vendor deliverables.
• Collaborate with Engineering, Manufacturing, Validation, Quality, and Facilities teams.
• Develop and review automation documentation including URS, FRS, SDS, control narratives, and system architecture.
• Support FAT, SAT, commissioning, startup, and CQV activities.
• Oversee PLC, DCS, SCADA, HMI, instrumentation, and control system implementation.
• Manage automation-related deviations, change controls, and Computer System Validation (CSV) activities.
• Ensure compliance with cGMP, GAMP 5, ASTM E2500, 21 CFR Part 11, and Data Integrity requirements.
• Serve as the technical lead for system integrators, contractors, and cross‑functional project teams.

Qualifications

• Bachelor's degree in Electrical, Chemical, Mechanical, Computer Engineering, or related field.
• 8+ years of automation engineering or automation project management experience in pharmaceutical, biotech, or life sciences.
• Strong knowledge of PLC, DCS, SCADA, HMI, instrumentation, VFDs, and industrial control systems.
• Experience with CSV, CQV, change control, FAT/SAT, commissioning, and GMP compliance.
• Proven experience managing automation projects, vendors, and cross‑functional teams.
• Excellent communication, documentation, and stakeholder management skills.