Executive, Production

Apotex Inc.

Responsible Packaging supervisor managing execution and compliance in the packaging process at Apotex. Involves planning, organizing, and supervising packaging activities while adhering to Good Manufacturing Practices.

Posted 7/18/2026full-timeBangalore • 🇮🇳 IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Good Manufacturing Practices (GMP) and Good Documentation Practices, with a strong focus on compliance, quality assurance, and effective communication within a team-oriented environment.

Highest-signal resume keywords

Good Manufacturing Practices (GMP)Visual InspectionBatch Record ReviewPreventive MaintenanceTeam Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Packaging Process ManagementCalibration and VerificationSOP PreparationContinuous Improvement ExecutionEquipment Operation

Soft Skills

Efficient CommunicationStrategic ThinkingProblem SolvingTeam Work

Certifications & Qualifications

B.ScB.PharmM.Pharm

Industry Keywords

CGMP ComplianceStatus LabellingIn-Process TestingEnvironmental MonitoringSafety and Compliance

About the role

Key responsibilities & impact

Responsible role holder in the Packaging process to manage, execute and supervise packaging related activities (operation and cleaning)
Plan, organize and coordinate in the execution of packaging activities (operation and cleaning)
Monitor and coordinate in the execution of Calibration/Preventive maintenance and verification of the Equipments/Instruments in packaging area as per schedule
Undergo and participate in relevant department and cross functional trainings in learning plan
Be a Qualified Operator and visual inspector to handle necessary activities in Packaging section
Perform visual inspection activity as per respective SOPS
Work inline with the cGMP requirement like Status Labelling, In-Process test execution, environmental conditions and pressure difference monitoring and weighing
Execute batch as per instruction given in batch document
Support and handle in execution of equipment break down & alarms, movement of equipment, material and parts
Follow and adhere to safety and compliance aspects in all production steps
Review Batch record, validation protocols, 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 need and compliance
Execute continuous improvement in the manufacturing process, equipment and instrument
Ensure cleanliness and housekeeping with proper status labeling procedure
Handle manpower relocation as per requirement
Collaborate as a team member to achieve all outcomes
Ensure personal adherence with compliance programs including Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies
Other relevant duties as assigned

Requirements

What you’ll need

Minimum degree in B.Sc/B.Pharm/M.Pharm
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
Minimum 3 - 5 years of experience in the production process

Benefits

Comp & perks

Health insurance
Paid time off
Professional development opportunities