Apotex, one of the world’s leading Canadian pharmaceutical companies, is inviting applications for the position of Executive โ Documentation (Production Operations Support) at its Bangalore manufacturing facility. This is an excellent opportunity for candidates looking to build a career in pharmaceutical production documentation, QMS, SAP, GMP, and manufacturing operations.
Candidates with 0โ5 years of experience who possess knowledge of QMS, TrackWise, SAP documentation, cGMP, and production documentation are encouraged to apply.
Job Details
| Particular | Details |
|---|---|
| Position | Executive โ Documentation โ Production Operations Support |
| Company | Apotex |
| Location | Bangalore, Karnataka |
| Experience | 0โ5 Years |
| Department | Production Operations Support |
| Employment Type | Full Time |
About Apotex
Apotex is a Canadian-based global pharmaceutical company committed to improving access to affordable medicines worldwide. With a broad portfolio of generic medicines, biosimilars, branded pharmaceuticals, and consumer healthcare products, Apotex operates across North America, India, Mexico, and several international markets.
The company offers professionals an opportunity to work in a highly regulated pharmaceutical manufacturing environment with global quality standards.
Key Responsibilities
Selected candidates will be responsible for:
- Preparing and reviewing batch manufacturing documents.
- Supporting documentation for new product launches and site transfer projects.
- Coordinating QMS activities and ensuring timely closure.
- Managing Change Control documentation.
- Updating SAP master data related to products.
- Preparing and revising SOPs, formats, and batch records.
- Supporting investigation of documentation-related deviations.
- Ensuring timely implementation of CAPA documentation.
- Maintaining compliance with cGMP requirements.
- Coordinating with cross-functional teams.
- Supporting production planning activities.
- Troubleshooting SAP ZDOC printing issues.
- Maintaining document control through Content Server.
- Ensuring regulatory compliance and quality documentation.
- Following company safety, ethics, and quality policies.
Required Qualifications
Applicants should possess qualifications such as:
- GBDM
- DCTTC
- Relevant pharmaceutical or manufacturing documentation background
Preferred Skills
Candidates with the following skills will have an advantage:
- QMS TrackWise knowledge
- SAP Master Data handling
- cGMP compliance
- Production documentation
- SOP preparation
- Batch Manufacturing Record (BMR) documentation
- CAPA documentation
- Change Control management
- Good teamwork and communication
- Time management
- Problem-solving abilities
Experience Required
- 0โ5 years of relevant pharmaceutical manufacturing experience.
Freshers with relevant knowledge may also be considered depending on business requirements.
Salary (Estimated)
Based on current industry standards for similar pharmaceutical manufacturing documentation roles:
โน3.8 LPA โ โน7.5 LPA (CTC)
Actual salary will depend on qualifications, experience, and company policies.
Why Join Apotex?
Working at Apotex provides numerous career advantages:
- Global pharmaceutical organization
- Exposure to international GMP standards
- Learning opportunities in SAP and TrackWise
- Strong documentation and quality systems experience
- Career growth in Production Operations
- Collaborative work culture
- Employee development programs
- Ethical and compliance-driven environment
How to Apply
