DeltaV Lead Engineer

Delta

V Lead Engineer – Life Sciences

Work Model:
Remote

Job Type: Full-time

Industry: Pharmaceutical / Biotech / Life Sciences

A Delta

V Lead Engineer in the life science industry is responsible for managing the implementation and maintenance of Emerson’s Delta

V automation system within pharmaceutical, biopharmaceutical, or biotechnology manufacturing environments. This role oversees Delta

V-related projects, ensures compliance with industry regulations, and provides deep technical expertise and support. The engineer will drive system performance, troubleshooting, documentation, and continuous improvement across the Delta

V ecosystem.

• Design, implement, maintain, and support Emerson Delta
  
  V systems in a GMP-regulated manufacturing environment.
• Troubleshoot and resolve technical issues related to Delta
  
  V hardware, software, and batch control strategies.
• Ensure compliance with cGMP, GAMP 5, 21 CFR Part 11, and other regulatory standards through proper validation and documentation.
• Lead and manage Delta
  
  V-related automation projects, including planning, scheduling, and resource coordination.
• Collaborate with cross-functional teams including Operations, IT, Engineering, and Quality to integrate Delta
  
  V with broader manufacturing processes.
• Provide ongoing maintenance, periodic reviews, and upgrades to ensure system integrity and performance.
• Develop and maintain technical documentation including design specifications, user manuals, SOPs, and change control records.
• Identify and implement continuous improvement opportunities within the Delta
  
  V system and related automation environments.
• Train operators, engineers, and maintenance personnel on Delta
  
  V system functionality, troubleshooting, and operational best practices.
• Support and collaborate on related technologies (PLC, SCADA, OSI PI, etc.) as needed.

• Proven hands‑on experience with Emerson Delta
  
  V system design, configuration, implementation, and support.
• Experience in pharmaceutical, biopharmaceutical, or biotechnology manufacturing environments.
• Strong understanding of automation principles including DCS, PLCs, and SCADA systems.
• Expertise in regulatory and validation frameworks (cGMP, GAMP 5, 21 CFR Part 11).
• Excellent analytical and problem‑solving skills with the ability to troubleshoot complex automation issues.
• Strong communication, collaboration, and documentation skills.
• Project management experience overseeing automation initiatives from concept to delivery.

The annual salary range for this position is in the range of $113,000 to $130,000, depending on experience, skills, and geographic location. This role may also be eligible for performance‑based bonuses in accordance with company compensation policies.

Travel – Readiness to travel as and when needed for project discussion, planning workshops with client, FAT and for Business Cut Overs

• Comprehensive medical, dental, and vision coverage
• 401(k) retirement savings plan with company match
• Paid time off (PTO), paid holidays, and wellness days
• Life insurance and disability coverage
• Employee Assistance Program (EAP) and mental health support
• Professional development, training, and certification reimbursement