Associate – MES | Pfizer | Vizag

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Job Overview

  • Date Posted
    October 25, 2023
  • Location (State / UT)
  • Expiration date
    February 20, 2025
  • Experience
    2 Years, 5 Years
  • Gender
    Male
  • Desired Qualification
    Bachelor Degree

Job Description

Role & Responsibilities:

  • Contribute to completion of project milestones and organize own work to meet project task deadlines.
  • Assess challenges to the schedule and re-directing activities as necessary to minimize impact on quality, compliance, and timelines.
  • Capable of detecting technical problems and assisting the appropriate colleagues for resolution.
  • Perform routine production preparation tasks such as preparing production glassware and other equipment by operating industrial washers, autoclaves, and dehydrogenation ovens, using calibrated scales to weigh out dry components, and using graduates and flasks to measure liquids.
  • Able to collect and assemble applicable, vital information for recommendations to Production Supervisors and/or Manufacturing Process Engineers to assist in troubleshooting and decision-making.
  • Organize daily functions and work in concert with Bioprocessing Technicians in executing operational aspects for Fermentation, Purification, and Conjugation processing in a compliant, safe, and efficient manner to maintain production schedules.
  • Understand scientific principles, operational aspects of production equipment, automation control systems, processing requirements, and any related procedural requirements.
  • Develop best practices and share them with other teams and sites.
  • Conduct all activities that are in accordance with company policies and Standard Operating Procedures, Pfizer Values, global regulatory guidelines, environmental guidelines, as appropriate, etc.
  • Perform laboratory activities such as performing sample dilutions, pH, and conductivity readings.
  • Provide input and revise Standard Operating Procedures, batch records, forms, or other {Current} Good Manufacturing Practices {part of GxP} related documents to support continuous improvement efforts, investigation corrective actions, etc.
  • Track and follow up on departmental commitments, investigations, change controls, change control, and general compliance initiatives.

Qualifications

Must-Have
  • Bachelor’s Degree
  • Demonstrated experience in Food and Drug Administration-regulated industry
  • Demonstrated experience within the biopharmaceutical industry, including knowledge and experience with relevant biopharmaceutical unit operations and/or laboratory operations
  • Ability to perform mathematical calculations and learn new processes
  • Proactive in engagement with key stakeholders
  • Excellent verbal and written communication skills
  • Ability to efficiently use current computer packages including Excel, PowerPoint, MS Project, and Word
Nice-to-Have
  • Experience in a biopharmaceutical or pharmaceutical {Current} Good Manufacturing Practices
  • Knowledge of operational aspects for Fermentation, Purification, and Chemistry processing