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Senior Executive - Global External Supply Operations

Apotex
5+ years
INR 10 LPA – 18 LPA
Bangalore, India
1 June 19, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Senior Executive – Global External Supply Operations (GES Operations)

Location: Bangalore, Karnataka, India
Company: Apotex Inc.
Employment Type: Full-Time

Role Summary

The Senior Executive – Global External Supply Operations (GES Operations) supports Product Lifecycle Management (PLCM) and Product Transfer programs by coordinating cross-functional projects, managing operational data, supporting supply chain activities, and ensuring seamless collaboration with external manufacturing partners.

This role acts as a Project Coordinator within the GES Operations team, providing project management support, dashboard reporting, partner coordination, material management, and process improvement initiatives to ensure uninterrupted product supply and successful execution of external manufacturing and supply chain projects.

Key Responsibilities

Project Coordination & Portfolio Support

  • Support the Global External Supply (GES) Operations portfolio of projects.

  • Coordinate Product Lifecycle Management (PLCM) and Product Transfer activities across multiple programs.

  • Monitor project timelines, milestones, and deliverables to ensure successful execution.

  • Maintain project trackers, schedules, and dashboards to provide visibility into project progress.

  • Support Project Managers and stakeholders in project planning and execution activities.

  • Ensure project information remains accurate and updated in project management systems.

Change Management & Regulatory Data Coordination

  • Initiate, track, and coordinate change requests related to:

    • SAP Material Codes

    • Master Recipes

    • Manufacturing Master Records (MMaRs)

    • Manufacturing Process Records (MPaRs)

    • Finished Goods

    • Semi-Finished Goods

    • Packaging Components

    • Unique Excipient Codes

  • Ensure timely processing and implementation of approved changes.

  • Support documentation updates and change control processes.

Supply Chain & Material Coordination

  • Coordinate material and sample shipments for:

    • Contract Manufacturing Organizations (CMOs)

    • Contract Packaging Organizations (CPOs)

  • Manage:

    • Material Requests

    • Sample Orders

    • Quotations

    • Documentation Requirements

  • Monitor inventory levels and shipment tracking.

  • Coordinate delivery activities and ensure material availability for project requirements.

Data Management & Reporting

  • Collect and consolidate project-related information from multiple stakeholders.

  • Support preparation of:

    • Technical Summaries

    • Project Reports

    • Operational Dashboards

    • Performance Metrics

  • Utilize systems and tools such as:

    • SAP

    • Enterprise Project Management (EPM)

    • SharePoint

    • Salesforce

    • Project Management Platforms

  • Generate reports and insights to support informed decision-making.

Partner & Stakeholder Coordination

  • Serve as a key liaison between internal teams and external partners.

  • Coordinate partner meetings and communication activities.

  • Prepare:

    • Meeting Agendas

    • Presentations

    • Meeting Minutes

    • Status Updates

  • Ensure partner information is maintained accurately in company databases.

  • Facilitate information sharing across cross-functional teams.

Product Lifecycle Management (PLCM) Support

  • Support end-to-end implementation of PLCM initiatives.

  • Ensure successful execution of changes impacting the GES product portfolio.

  • Collaborate with stakeholders to maintain uninterrupted product supply.

  • Support launch readiness and commercialization activities.

  • Track regulatory and operational milestones related to product changes.

Process Improvement & Operational Excellence

  • Participate in cross-functional initiatives focused on:

    • Process Optimization

    • Operational Excellence

    • Continuous Improvement

  • Contribute to the development of:

    • Systems

    • Policies

    • Procedures

    • Performance Metrics

  • Analyze operational and supply chain data to identify improvement opportunities.

  • Support implementation of best practices across GES Operations.

Cross-Functional Collaboration

  • Collaborate with:

    • Supply Chain Teams

    • Manufacturing Operations

    • Quality Assurance

    • Regulatory Affairs

    • Technical Services

    • External Manufacturing Partners

  • Facilitate communication and alignment across functions to achieve project objectives.

  • Support commercial readiness and supply continuity initiatives.

Compliance & Organizational Responsibilities

  • Ensure compliance with:

    • Global Quality Policies

    • Business Ethics Programs

    • Safety & Environmental Policies

    • Company SOPs

  • Demonstrate organizational values:

    • Collaboration

    • Courage

    • Perseverance

    • Passion

  • Promote a safe and compliant working environment.

  • Perform additional duties as assigned to support business needs.

Required Qualifications

Education

One of the following qualifications:

  • Bachelor of Science (B.Sc.)

  • Diploma in:

    • Engineering

    • Chemistry

    • Biology

    • Pharmaceutical Sciences

    • Health Sciences

    • Related Discipline

Preferred Qualifications

  • Project Management Certification (PMP) or equivalent is considered an advantage.

Experience

  • Minimum 5 years of experience in:

    • Pharmaceutical Industry

    • Supply Chain Operations

    • Manufacturing Operations

    • Research & Development Environment

    • Project Coordination Roles

  • Minimum 1 year of experience using:

    • Microsoft Project

    • Other Project Planning Software