Sr. Associate - Projects

☞ Cognizant

見る: 165

更新日: 16-11-2025

場所: Brussels Brussels Capital

カテゴリー: IT-ソフトウェア IT-ハードウェア/ネットワーキング 情報技術 機械/技術 メンテナンス

業界: IT

Loading ...

仕事内容

Equipment and Automation Integration Lead
Requirement is to author recipes per site requirements

Main Responsibilities:

  • Perform workshops to conduct Requirements gathering and analysis with the site team too understand manufacturing processes
  • Prepare functional specification based on requirements for EBRs
  • Prepare As-Is and To-Be mapping documents
  • Identify Rockwell FTPS MES system building blocks (new / Remediation) needed for creating recipe templates
  • Design Global Weigh and Dispense and EBR templates.
  • Configure Master Recipes and Master data in MES system
  • Conduct testing and demos of master recipes with site teams
  • Deployment of Global templates for Weigh and Dispense at site
  • Support to develop and/or update SOP’s
  • Participate in IQ, OQ and PQ
  • Assist in preparation of SOP’s and other documentation for recipes
  • Preparation of training content development
  • Train the end-users and sme’s as needed
  • Mentor site Master Recipe Authors through EBR Recipe Life Cycle
  • Liaise with business and vendor to resolve complex technical problems
  • Provide EBR Go-Live and Hyper care support
  • Migration of site legacy MES and paper based recipes to the new Rockwell FTPS MES Solution utilizing the Global templates

Skills required:

  • Minimum 6 to 8 years’ experience as Recipe Authoring using Rockwell Factory Talk Pharma Suite MES in Pharma environment
  • Should have been part of an end-end MES deployment for Pharma Industry using Rockwell FTPS MES system
  • Preparation of MBRs, Recipe Templates and recipes across various Pharma Manufacturing processes
  • Modelling Manufacturing processes in Pharma
  • Strong oral and written communication skills are required, with proven ability to communicate and build relationships cross-functionally
  • Self-motivated, ability to work independently or under minimum supervision


Desired Skills:

  • Good understanding of Biotech pharma manufacturing processes
  • Knowledge of 21CFR Part 11 requirements, ER/ES and data integrity guidelines
  • Experience of working in a GMP environment
  • Experience working on integration of Manufacturing IT systems and other automation/L3 systems

Employee Status :Full Time Employee

Shift :Day Job

Travel :No

Job Posting :Aug 31 2021

About Cognizant
Cognizant (Nasdaq-100: CTSH) is one of the world’s leading professional services companies, transforming clients’ business, operating and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant is ranked 185 on the Fortune 500 and is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at www.cognizant.com or follow us @Cognizant.
Loading ...
Loading ...

締切: 31-12-2025

無料の候補者に適用するにはクリックしてください

申し込む

レポートジョブ
Loading ...

同じ仕事

Loading ...
Loading ...