Job Description

Essential Functions:

  • Operate autoclave equipment and associated sterilization apparatus in compliance with established SOPs and GMP requirements
  • Support sterilization cycle operations including loading, unloading, and monitoring of autoclave processes to meet product specifications
  • Perform general maintenance on autoclave equipment and associated apparatus as required to ensure operational readiness
  • Execute standard operating procedures to meet current Good Manufacturing Practices (cGMP) requirements for sterile manufacturing
  • Maintain accurate batch documentation records in compliance with regulatory and internal requirements
  • Ensure all tasks are completed in full compliance with applicable regulatory requirements including FDA and EMA guidelines
  • Participate in process improvement projects to enhance quality, cost efficiency, and production scheduling
  • Conduct area cleaning and sanitization activities in accordance with cleanroom and aseptic GMP standards.
  • Responsible for operation and cleaning of dynamic pass box in autoclave area.
    •To carry out CIP & SIP of the vessels related to autoclave area.
    •Responsible for operation and cleaning of area equipment present in the autoclave area like Pass boxes,
    Glove cleaning and integrity testers.
    •Preparation, filtration and issuance of disinfectant and deactivation solutions to all the sections in the
    production area.
    •Operation and cleaning of table mounted LAF and Ceiling mounted LAF and steam sterilizer and HPHV
    steam sterilizer.
    •Preparation of loads meant for Autoclaving like garments, disinfectant, filling, filtration, rubber stopper and
    seals for sterilization as per the validated load pattern.
    •Responsible for Maintenance and cleaning of Component preparation and sterilization area (Autoclave
    area).
    •Cleaning and sanitization of drain points in Component preparation and sterilization area (Autoclave
    area).
    •Monitoring of DP, RH and temperature in compounding and filtration area, autoclave area.
    •Responsible for timely completion of calibrations and validations activity in coordination with Engineering
    and QA related to autoclave area.


Job Details

Role Level: Associate Work Type: Full-Time
Country: India City: Hyderabad ,Telangana
Company Website: http://www.amneal.com Job Function: Manufacturing & Production
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


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