Associate - MES

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Vizag, Vishākhapatnam, Andhra Pradesh
Hybrid
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Job Description:
  • To Design and simulate AMPS (Agile manufacturing production system) recipe towards ease of user execution and ensuring its feasibility as per site requirements.
  • Ensuring recipe readiness per weekly manufacturing plan.
  • Preparation/revision of Electronic Batch Records (EBR) based on the approved MMR/MBR/Validated Documents.
  • Supporting end users on EBR execution/usage.
  • Troubleshoot and solve AMPS/SAP/MLM problems and to get in depth/detailed understanding/identify root cause.
  • To proactively handle activities in Implementation projects and enhancements.
  • Tracking of all documentation activity i.e., SOP revision, CAPA closure, change controls, change action items and investigation
  • Be the first point of contact for electronic manufacturing issues.
  • Escalation of Electronic manufacturing execution issues to Shift Manager-MES or supporting teams.
  • Having thorough knowledge of Manufacturing execution system (MES).
  • Conducting trainings to executing personnel on EBR system.
  • Handling of Shop floor troubleshooting in SAP- AMPS interface.
  • Tracking of AMPS (Agile manufacturing production system) recipes revision as per revised/new batch records.
  • Creation of Bill of Material (BOM) and production version (PV) in SAP.
  • Ensuring readiness of Bill of Material (BOM) and production version (PV) in SAP required to create AMPS recipes.
  • Handling of SAP (System Application and Products) related issue and shop floor support.
  • SAP stock clearance, IDOC message clearance.
  • BT ticket follow ups and ensuring its resolution with batch release tracking.
  • To participate and execution of new upcoming MES projects.
  • Handling/Designing and to ensure smooth running of Manufacturing label management (MLM) system.
  • Coordinate supporting functional departments for smooth operation of production activities.
  • Ensure compliance of operations to cGMP, safety and Pfizer integrity principles at all stages of activity
  • To participate in internal & external (regulatory & non-Regulatory) audits.

Qualifications
Must-Have
  • Batchelor degree
  • 5+ years of experience
  • Have knowledge on AMPS application and participated in BV execution.
  • Demonstrated ability to understand and follow written procedures, can work independently or in groups effectively

Nice-to-Have
  • Master's Degree

Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Information & Business Tech

What the Team is Saying

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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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