EXECUTIVE

Biocon

$90K — $120K *
Media, PA 19063In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.Sc. degree in relevant field
  • 2-6 years of experience in production processes
  • Familiarity with fermentation and media preparation operations
  • Experience with equipment qualifications and QMS activities
  • Knowledge of automation systems (DCS, MES, EMS)
  • Ability to perform data entry with attention to detail

Responsibilities

  • Monitor and handle fermenters, nutrient dosing, and media preparation vessels
  • Conduct equipment cleaning and ensure diabetes and housekeeping compliance
  • Perform calibration of pH meters and verify weighing balances
  • Assist in raw material and product inventory management
  • Conduct in-process product sampling and data entry in quality records
  • Coordinate with maintenance and instrumentation teams for equipment upkeep
  • Execute equipment qualifications and prepare production-related documents

Benefits

  • Opportunity to work with advanced automation systems
  • Collaboration with cross-functional teams such as QA and maintenance
  • Focus on adherence to industry best practices (GMP, GDP)
  • Engagement in continuous learning through SOP and production documentation prep
  • Involvement in QMS activities including audit preparation
Full Job Description
Department Details

Production-Upstream

Role Summary

  • To handle operations of Fermenters, Nutrient dosing vessels, Media preparation vessels and CIP tanks
  • To perform equipment cleaning, monitoring and ensure housekeeping activities
  • Calibration of pH meters and Standard weights verification of weighing balances
  • Monitoring and maintenance of raw material / Product inventory in co-ordination with superiors.
  • In-process product sampling
  • Data entry in Quality records
  • Coordination with Maintenance and Instrumentation team for maintenance and breakdown activities


Key Responsibilities

  • To perform and execute equipment qualifications and requalification's
  • Real time data entry in Quality records
  • Handling of e-BMR (SAP) activities.
  • Sound knowledge on Automation systems like DCS / MES / EMS
  • Handling of QMS activities (CCF, Deviations and OOS etc.)
  • Preparation of SOPs, EOPs, OCPs, BMR and production related documents.
  • To coordinate with QA for all the validation, qualification and Audit preparedness
  • Adherence to Standard Operating Procedures, product specifications.
  • Adherence to Good manufacturing Practices and Good Documentation Practices


Educational Qualifications

Required Education Qualification: B.Sc
Required Experience: 2 - 6 years

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