Principal - Engineer - Automation; DeltaV System Administrator

Responsibilities

• Support the design and delivery of process automation systems (requirements, verification plans, validation plans, and computer system validation strategies) for Emerson Delta
  
  V DCS platforms.
• Perform hardware design for the site Delta
  
  V DCS platform, including site administrative procedures and validation.
• Support related site automation platforms (secondary):
  Data Historians and process automation servers.
• Collaborate with Lilly Quality, A&E firms, system integrators, Emerson, and corporate/site engineering peers.
• After project delivery, support GMP manufacturing operations via Delta
  
  V system administration services and platform upgrades.

• Champion safety culture; mentor and coach others; apply engineering/automation fundamentals.
• Become a subject matter expert on Lilly’s Delta
  
  V reference architecture to create site Delta
  
  V platform design.
• Support Delta
  
  V platform design, delivery, validation, and system management.
• Lead/direct system integrations and OEMs for Delta
  
  V platforms, data centers, and associated infrastructure.
• Collaborate to develop computer system qualification and testing strategies.
• Ensure CSV documents comply with corporate/local standards, templates, and electronic document management properties.
• Participate in basic/detailed design including staffing, statements of work, supplier management, and CSV delivery strategies.
• Develop/build capabilities within the Houston site automation team.
• Support development of site procedures for CSV and administration practices and provide technical oversight for equipment/process system User Requirements and Design Review/Qualification documentation.

• Bachelor’s degree in engineering or related Science degree (required).
• 3+ years Emerson Delta
  
  V system administration experience, including hardware design.
• Windows Servers and virtual environments experience.
• Process automation experience.
• 3+ years pharmaceutical manufacturing experience (other manufacturing considered).

• Strong analytical, writing, and critical thinking skills.
• Experience with Kneat Validation and/or Veeva Vault (or similar).
• Ability to collaborate with others.

Travel potential (