Senior Officer - Quality Control

Job Summary

Calibration of standalone instruments, maintenance of portable instruments and preventive maintenance of QC laboratory instruments and  coordinating with Service engineers for the breakdown of instruments.

Job Responsibilities

• Daily verification/Calibration of pH Meter, Conductivity Meter and balances.
•  Calibration activity of Instruments as per schedule
• Maintenance activity of hibernated instruments in other laboratories (Commercial Stabilty laboratory Analytical Research and development 1&2 and  PE&DS)

• Follow Compliance of cGLP in Quality Control Laboratory.
• In co-ordination with the service engineer ensuring smooth function of all laboratory instruments.
• Updation of calibration schedule/ preventive maintence schedule as well as instruments calibration label.
• Maintenance of Portable instruments and co-ordination with engineer team for schedule calibration activity.
• Coordinating with Service engineers for the breakdown of instrument.
• Perform all work in support of our Corporate Values and Demonstrates strong and visible support of our values.
• Perform all work in accordance with all established regulatory and compliance and safety requirements.
• Perform all other duties as assigned by Head of the Department\Designee.
• Works in a safe manner  collaborating as a team member to achieve all outcomes.
• Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
• Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. 
• All other relevant duties as assigned.

Job Requirements

• Education
  • Minimum MSc/BPharm or any equivalent degree

• Knowledge, Skills and Abilities
  • Effective command over verbal and written communication with good interpersonal skills
  • Command on Microsoft-Office (Word, Excel)
  • Best in effective planning of work activities to meet the time lines
• Experience
  • Minimum 2 to 4 years of experience in GMP regulated Pharmaceutical Industry