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• Our client is seeking an experienced CSV Migration Consultant to support the implementation, migration, and validation of critical manufacturing systems within a regulated environment.
• This role requires deep expertise in automation and computerized system validation, particularly with Rockwell and Pharma Suite platforms.
• The ideal candidate will have a strong background in the full CSV lifecycle, regulatory compliance, and the ability to work in both independent and collaborative settings.
  
  

• Our client is seeking an experienced CSV Migration Consultant to support the implementation, migration, and validation of critical manufacturing systems within a regulated environment.
• This role requires deep expertise in automation and computerized system validation, particularly with Rockwell and Pharma Suite platforms.
• The ideal candidate will have a strong background in the full CSV lifecycle, regulatory compliance, and the ability to work in both independent and collaborative settings.
  
  

• Lead the implementation, migration, and validation of computerized systems, including PCS (Rockwell/Client), MES (Pharma Suite, POMSnet), and SCADA/PLCs.
• Apply hands-on expertise in programming, commissioning, and validating Rockwell and Pharma Suite platforms.
• Author, review, approve, and execute CSV lifecycle documentation in compliance with applicable procedures and industry standards.
• Ensure adherence to SDLC principles and regulatory requirements, including 21 CFR Part 11, Annex 11, GAMP 5, and Data Integrity guidelines.
• Manage, document, and assess software changes throughout the SDLC.
• Collaborate with cross-functional teams to ensure seamless integration and operational excellence.
• Utilize knowledge of S88 Batch Standard for batch process design.
• Perform MES recipe authoring and testing, as well as Rockwell software object development.
• Support system validation activities using Kneat.
  
  

• Experience supporting medium-to-large-scale capital projects in a procurement or expediting function.
• 12+ years of CSV/Automation experience in a regulated environment.
• Strong, hands-on experience with Rockwell and Pharma Suite (required).
• Proven track record in implementing and validating PCS, MES, SCADA, and PLC systems.
• In-depth knowledge of SDLC, 21 CFR Part 11/Annex 11, Data Integrity, and GAMP 5 guidelines.
• Experience with software change management and documentation practices.
• Familiarity with S88 Batch Standard, Rockwell software object development, and MES recipe authoring/testing is preferred.
• Experience with Kneat or other validation management tools is preferred.
• Excellent verbal and written communication skills.
• Ability to work independently and collaboratively within a team-oriented environment.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Information Technology

• Industries

  Business Consulting and Services

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