Walkin Drive- ProductionEnggQA (Sterile formulations) Hyderabad

About Client: Client is among the Top 10 Pharmaceutical company in India cater to both domestic and international markets with a diverse portfolio of Formulations and APIs.

For Operators:

• • Operate and monitor equipment in aseptic and non-aseptic areas (vial washing filling sealing lyophilization autoclaves etc.).
  • Perform routine production activities as per SOPs and batch records.
  • Ensure adherence to cGMP safety and EHS guidelines during operations.
  • Carry out cleaning sterilization and line clearance activities.
  • Record data accurately in logbooks and batch manufacturing records.
  • Support preventive maintenance and calibration activities.

For Executives:

• • Supervise and coordinate day-to-day production activities in sterile injectable areas.
  • Review and ensure compliance of batch records SOPs and regulatory requirements.
  • Monitor aseptic practices and environmental controls during production.
  • Train and guide operators on GMP safety and process improvements.
  • Handle deviations change controls and CAPA implementation.
  • Liaise with QA QC Engineering and EHS teams for smooth operations.
  • Drive continuous improvement initiatives for yield efficiency and compliance.

Instrumentation Maintenance of Process

• • Perform routine calibration preventive maintenance and troubleshooting of PLC SCADA sensors transmitters controllers and automation systems in sterile equipment (bioreactors fermenters chromatography skids filtration units autoclaves clean steam generators).
  • Ensure accuracy of critical process parameters (temperature pressure flow pH DO conductivity).
  • Maintain and update calibration records logbooks and electronic systems in compliance with GMP.
  • Support qualification and validation of new instrumentation and equipment.

Skills & Competencies

• • Strong knowledge of sterile manufacturing processes and regulatory standards (USFDA EU GMP WHO).
  • Hands-on experience with injectable production equipment.
  • Attention to detail and documentation accuracy.
  • Ability to work in controlled environments (Grade A/B/C/D).
  • Good communication and teamwork skills.

Experience Required

• • Operators: 2-8 years in sterile/injectable production.
  • Executives: 3-8 years in sterile/injectable production with supervisory exposure.

Why Join Us

• • Opportunity to work in a world-class sterile manufacturing facility.
  • Exposure to global regulatory standards and audits.
  • Career growth in a fast-expanding pharmaceutical organization.