Perform and report analysis of raw material samples (API, excipients, packing material, and water samples) using various analytical instruments.
Job Responsibilities
- Analysis of raw material samples as per method of analysis by adhering to regulatory procedures and trending of raw materials.
- 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 a priority basis.
- Provide technical support to Apotex group of companies during activities like technology transfer.
- Perform all work in accordance with all established regulatory, compliance, and safety requirements.
- Work in a safe manner, collaborating as a team member to achieve all outcomes.
- Demonstrate behaviors that exhibit our organizational values: Collaboration, Courage, Perseverance, and Passion.
- Ensure personal adherence to all compliance programs, including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
- Perform 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.
- Proficient in Microsoft Office (Word, Excel).
- Able to prioritize tasks.
- Skilled in effective planning of work activities to meet timelines.
