Quality Control Jobs at Apotex | Chemistry Graduates Apply Now
Are you looking for quality control jobs in a reputed pharmaceutical company? Apotex is hiring for the role of Quality Officer – Commercial Stability Laboratory in Bangalore. This opportunity is ideal for professionals seeking stable Apotex jobs with hands-on exposure to GMP-regulated laboratory environments and long-term career growth. Candidates with relevant experience and an MSc background can take the next step in their pharma careers with this opening.
- Location: Bangalore, KA, IN, 560099
- Company: Apotex
About Apotex Inc.
Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico, and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.
Job Summary
Analysis of Stability samples, Method verification, Method transfer sample and Instrument qualifications as assigned in a timely manner.
Job Responsibilities
- Analysis of Stability analysis, Method verification, Method transfer samples as per method of Analysis by adhering to the Regulatory Procedures.
- To be responsible for all activities in the Commercial Stability Laboratory, including cGLP, documentation and implementation of departmental Quality systems.
- Qualification and calibration of analytical instruments as per the procedure.
- Performing timely analysis of samples on a priority basis.
- To ensure compliance with cGLP by following applicable procedures in the Laboratory.
- Compliance with GLP, SOPs, Test Procedures and Protocols, etc.
- Participate in the activities, ensuring all-time audit readiness in the lab.
- Assist in the reparation, review and revision of SOPs, test procedures as required.
- 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 the concerned department and taking efforts to resolve the same immediately. 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 the Assistant Manager.
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 timelines.
Experience
Minimum 1 to 2 years of experience in the GMP-regulated Pharmaceutical Industry.
Link to Original Notification to apply: Apply Here
