Walk -In Drive - Quality Control Bidar Location

Sai Life; Bidar District; On-site; INR 500,000 - 700,000; Full time

Job summary

Sai Life Sciences Limited in Bidar, Karnataka, invites candidates for a walk-in drive to join the Quality Control team. The role focuses on analytical testing of raw materials, intermediates, in-process samples, and finished products using HPLC and GC methods.

Candidates should be familiar with Empower software and GMP practices. Responsibilities include instrument calibration, data entry in GMP Pro, and adherence to SOPs during all QC activities.

Qualifications

• Experience in analytical QC testing in pharma/lab environment.
• Knowledge of HPLC/GC methods and related documentation.
• Familiarity with GMP/GLP practices.

Responsibilities

• Perform HPLC and GC analysis on raw materials, in-process samples, and finished products.
• Record environmental conditions (temperature and humidity) in the lab.
• Operate and calibrate instruments per SOPs.

Skills

HPLC analysis

GC analysis

Empower Software

Calibration

Tools

GMP Pro

Job description

Walk -In Drive - Quality Control Bidar Location Bidar, Bidar, Karnataka, India ..+ 2 2 - 8 Years Permanent

Job Description

Key Responsibilities

• Responsible to perform the HPLC analysis / GC analysis of Raw material & intermediates, in process/cleaning, intermediate, finished product and stability samples as per the work allotment.
• Record the Temperature and % Relative Humidity in the Laboratory.
• Knowledge of Empower Software.
• Good communication& Interpersonal skills.
• Check the Calibration, Preventive maintenance and status tag of the instruments prior to use.
• Operate and calibrate the instruments as per SOP.
• Print the ARDS from GMP Pro and enter the test results after completion of the analysis.
• Ensure the instrument log entries in GMP Pro after completion of each activity during the analysis.
• Send the samples for other laboratory testing (internal/external) as per the procedure.
• Maintenance and storage of all Chemicals, columns and Standards.
• Discard the samples as per the disposal procedure upon satisfactory verification of batch release status.
• Handover the solid and liquid waste to ETP for disposal as per the procedure.
• Check the validity of Chemicals, Reagents, Reference/Working Standards and instruments prior to use.
• To Co-ordinate with the supervisor in preparation of Investigation reports in the event of OOS, OOT and deviations.
• Report all the departmental activities to the immediate supervisor and HOD.
• Assisting the Head of the department for all QC related activities.
• Attend for the scheduled and unscheduled OJT/GMP trainings.