Apotex is hiring for the Trainee, GBS-AGO-SiteSupport-GBS-AGOSS position in Mumbai, India. This opportunity is suitable for candidates with a Bachelor’s or Master’s degree in Science or Pharmacy and 0–1 year of pharmaceutical industry experience.
The role focuses on Master Production and Packaging Documents (MPPDs), change control impact analysis, document management, SAP product master support, and compliance with current Good Manufacturing Practices (cGMP).
Apotex Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | Apotex |
| Job Title | Trainee, GBS-AGO-SiteSupport-GBS-AGOSS |
| Job Location | Mumbai, India – 400079 |
| Job Type | Trainee |
| Experience | 0–1 year |
| Qualification | Bachelor’s or Master’s degree in Science or Pharmacy |
| Job Posting Date | October 14, 2026 |
| Industry | Pharmaceutical |
About Apotex
Apotex is a Canadian-based global health company that provides affordable medicines and health products. Its portfolio includes generic, biosimilar, innovative branded pharmaceuticals, and consumer health products. The company is headquartered in Toronto and has regional offices globally, including in India.
Official website: www.apotex.com
Job Responsibilities
Candidates selected for the Trainee, GBS-AGO-SiteSupport role will be responsible for supporting pharmaceutical manufacturing documentation and related processes.
Key responsibilities include:
- Creating, reviewing, executing, and cancelling Master Production and Packaging Documents (MPPDs).
- Managing Material Masters and Master Recipes for GTA sites.
- Performing impact analysis for change control packages in collaboration with cross-functional and Quality teams.
- Compiling supporting documentation, including mark-ups and reports.
- Reviewing manufacturing instructions and ensuring the accuracy of master documents.
- Managing investigation sub-records, including F8s and F9s, and following up on product master blocking and unblocking in SAP.
- Preparing weekly and monthly reports and supporting relevant project approval and readiness activities.
- Ensuring changes comply with cGMP regulations, corporate standards, Standard Operating Procedures (SOPs), and work instructions.
- Supporting updates to commercial master documentation based on recommendations from Validation and Technical Operations.
- Identifying and reporting discrepancies, anomalies, and documentation errors.
- Developing and revising Standard Operating Documents related to manufacturing support.
- Coordinating with internal and external stakeholders to resolve issues and escalate critical concerns.
Eligibility and Qualifications
Candidates applying for the Apotex Trainee position must meet the following requirements:
- Educational qualification: Bachelor’s or Master’s degree in Science or Pharmacy.
- Work experience: 0–1 year of experience in the pharmaceutical industry.
- Document management: Working knowledge of a document management system is required.
Required Skills
Applicants should possess the following skills:
- Proficiency in Microsoft Office tools.
- Excellent verbal and written communication skills.
- Ability to work with online modules and software.
- Understanding of document management systems.
- Flexibility and the ability to multitask in a rapidly changing work environment.
- Ability to collaborate with cross-functional teams and manage stakeholder relationships.
- Attention to detail when reviewing manufacturing and packaging documentation.
