Baxter Supervisor, Microbiology
Are you
looking for a career that matters?
We believe
every person deserves a chance for a healthy life, free from illness and full
of possibility. We see a world full of healing, with viable care options
available to those with limited choices today. We envision new ways of
providing physicians, pharmacists and nurses with technologies that not only
treat chronic diseases, but also work to prevent them. We’re looking for team
members who are motivated to learn, grow and innovate, while making a
meaningful difference for millions of people around the world.
Key Roles
& Responsibilities: -
To review the
Master protocols and take approval of superior.
To review the
Standard Operating Procedure (SOP) according to the current regulatory
requirements and forward to Department Head for final approval.
To ensure the
clean environment for sterile preparation by implementing the Good
Manufacturing Practice (GMP) norms as per the international standards and
guidelines.
To review the
yearly calendar such as calibration and Performance Qualification (PQ)
Calendars.
To ensure
calibration and validation of instruments in microbiological laboratory.
To review and
approve reports of microbiological validations.
To establish
test protocol designs for scientific validation of test methods, equipment and
instruments used in testing or monitoring aspects of product quality.
To ensure
that BET, Bioburden and Sterility test are conducted as per the schedule.
To ensure
other periodic microbiological tests as per Standard Operating Procedure (SOP).
To capture
the abnormalities in the process, system or documents and resolve them
according to Quality management system.
To carry out
investigation in case of Out of specifications (OOS) and take the corrective
and preventive actions (CAPA).
To suggest effective
Corrective and Preventive Action (CAPA) for the abnormalities observed and
ensure its implementation.
To keep track
of regulatory commitments and ensure fulfilment of the same.
To
periodically conduct the training programmes for the personnel working in the
clean room to ensure the effectiveness of the same on Good Manufacturing
practices, Good Laboratory Practices, health, hygiene and maintenance of clean
room environment by following the right procedure.
To look after
the administration of personnel to ensure that they are adequately supported,
trained, developed and adhere to the quality standards.
TO VIEW & APPLY CLICK HERE
FOR MORE JOB UPDATES
No comments:
Post a Comment