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.

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

Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.