Analysis of Raw material samples as per method of Analysis by adhering to the Regulatory Procedures, Trending of Raw materials.
To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental Quality systems.
Performing Timely Analysis of Raw material Samples on Priority Basis.
To provide technical support to Apotex group of companies during activities like technology transfer.
Performs all work in accordance with all established regulatory and compliance and safety requirements.
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.
Qualification & Experience
MinimumMSc/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.