Executive - Production
Date: Jun 5, 2026
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.
For more information visit: www.apotex.com.
Job Summary
Responsible role holder in the Packaging process to manage, execute and supervise packaging related activities (operation and cleaning) and general activities as per the procedure and current Good Manufacturing Practices(cGMP) standards with Good documentation practices (GDP).
Job Responsibilities
- To plan, organize and co-ordinate in the execution of packaging activities (operation and cleaning).
- To monitor and coordinate in the execution of Calibration/Preventive maintenance and verification of the Equipments/Instruments in packaging area is done as per the schedule and status verified.
- To undergo and participate in relevant department and cross functional trainings (as and when assigned) in learning plan.
- To be a Qualified Operator and visual inspector as per Qualification process to handle necessary activities in Packaging section.
- To perform visual inspection activity as per respective SOPS.
- To work inline with the cGMP requirement like (But not limited to) Status Labelling, In-Process test execution, environmental conditions and pressure difference monitoring and weighing.
- To execute batch as per instruction given in batch document.
- To support and handle in the execution of equipment break down & alarms, movement of equipment, material and parts.
- To follow and adhere to safety and compliance aspects in all the steps in the production area.
- To review Batch record (MMaR), validation protocols, CPV, trail/Optimization and Placebo batches.
- Preparation and review of URS for new equipment/ instrument and involve in IQ, OQ, PQ of the equipment.
- Preparation of SOP as per the need and compliance of same.
- To execute continuous improvement in the manufacturing process, equipment and instrument.
- To ensure the cleanliness and housekeeping with proper status lableing procedure.
- Handling and relocation of manpower as per requirement.
- 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.
Responsabilités inhérentes à l’emploi
Job Requirements
- Education
- Minimum degree in B.Sc/B.Pharm/M.Pharm
- Knowledge, Skills and Abilities
- Proficient knowledge of Good Manufacturing Practices (GMPs) & Good Documentation Practices.
- Efficient communication, strategic thinking and problem solving skills.
- Adequate knowledge to understand the written procedures and policies.
- Team work and communication skills.
- Experience
- Minimum 3 - 5 years of experience in the production process
Exigences liées au poste
At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed.
We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.