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MES Engineer / PharmaSuite Consultant

Optiwisers

MES Engineer / PharmaSuite Consultant (Onsite – Parsippany, NJ)

We are currently looking for an experienced MES Engineer / Rockwell PharmaSuite Consultant to join an urgent project with a leading client in the Life Sciences Manufacturing industry in the United States.

This is an onsite role based in Parsippany, New Jersey , requiring daily presence at the client site.

Key Responsibilities

  • Review, analyze, and understand current (“As-Is”) and future (“To-Be”) business process flows and URS documentation provided by Business and MES SMEs
  • Build and update design specifications and related validation documentation in collaboration with the CSV Lead
  • Coordinate approvals with relevant stakeholders
  • Configure MES solutions and L2 (Automation) interface tags as required
  • Develop FTPS Procedure Templates and Master Recipes
  • Perform demos and informal verification of recipes in Development/Sandbox environments
  • Update recipes based on business feedback and evolving requirements
  • Create and maintain OQ protocols
  • Prepare and execute test scripts, supporting validation and CSV activities
  • Follow up with stakeholders for reviews and approvals
  • Support updates to CSV documentation including VP, FS, DS, OQ, PQ, TM, and validation reports
  • Assist Business and Site IT teams in migrating recipes to Quality and Production environments
  • Support OQ/UAT, PQ activities, and Go-Live execution
  • Deliver training to Super Users and SMEs using a Train-the-Trainer approach
  • Provide hypercare support for eBR-related production issues
  • Conduct Knowledge Transfer (KT) sessions with MES support teams post-hypercare

Required Skills & Experience

  • Strong experience with Rockwell PharmaSuite MES
  • Experience in Life Sciences / Pharmaceutical Manufacturing environments
  • Hands-on experience with MES recipe design, configuration, testing, and deployment
  • Good understanding of CSV and validation processes
  • Experience preparing and executing OQ/PQ documentation and test scripts
  • Ability to work closely with Business, IT, Automation, and Validation teams
  • Strong communication and stakeholder management skills

Location

  • Onsite in Parsippany, NJ
  • Candidates must be able and willing to work at the client site daily

Start Date

  • Urgent requirement / Immediate availability preferred

Vacancy posted 4 days ago
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