Senior Officer, CommStblyLab-ARPL-CSA AR

Job Summary

Perform and report of analysis of Stability, Inprocess and Finished products, Cleaning Method validation analysis by using various analytical instruments.

Job Responsibilities

• Analysis of Stability, Inprocess and Finished products samples, Cleaning Method validation as per method of Analysis by adhering to the Regulatory Procedures.
• To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental Quality systems.
• Performing timely analysis of Inprocess and Finished products samples on priority basis.
• Performs all work in accordance with all established regulatory and compliance and safety requirements.
• Coordinating the issues related to the specifications/ worksheets/ other documents with concern department ans take efforts to resolve the same immeadiately.Identify the causes and recommend/implement solutions with management oversight.
• 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 by supervisor.

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).
  • Able to prioritize the tasks.
  • 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.