Pharma Manufacturing and Technology Transfer Job Opportunity for M Pharmacy Graduates | Apotex Careers | Apply Now
If you are searching for a Pharma Job in the pharmaceutical industry, Apotex Careers has announced an exciting opportunity for professionals in Manufacturing Science & Technology. This Pharma Job for the position of Senior Executive MS&T in Bangalore is ideal for candidates with experience in technology transfer, process validation, and product lifecycle management. Through Apotex Careers, professionals can join a global pharmaceutical company focused on improving access to affordable medicines worldwide.
- Job Title: Senior Executive MS&T
- Location: Bangalore, KA, IN, 560099
About the Company
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.
Job Description
- Support site technology transfer of products to Apotex Research Private Limited (ARPL), India.
- Manage technology transfer of new products from formulation development to commercial manufacturing.
- Provide technical support for troubleshooting manufacturing process issues in commercial batches.
- Assist in Product Life Cycle Management (PLCM) to ensure process and product robustness.
- Handle supplier-driven changes (SDC) related to API and excipient sources.
- Provide documentation support for MS&T activities.
Key responsibilities
- Prepare, review, and update SOPs, validation documents, and technical reports.
- Support technology transfer and new product launches.
- Perform cleaning validation, risk assessments, and process validation activities.
- Review APQR reports and product data trending.
- Assist in regulatory audits and ensure GMP compliance.
- Coordinate manufacturing process validation and batch monitoring.
- Provide technical support for manufacturing troubleshooting.
- Prepare technical documentation for product lifecycle management and site transfers.
- Support quality risk management, change control, and TrackWise documentation.
- Collaborate with manufacturing, QA, and other departments to resolve technical issues.
Qualification
- Education: Master’s Degree in Pharmacy
Knowledge, Skills, and Abilities
- Strong knowledge of solid dosage process development and technology transfer for regulated markets.
- Good understanding of product development, scale-up, and process validation.
- Knowledge of clinical and regulatory requirements for USA, Canada, Australia, and EU markets.
- Good communication, interpersonal, and MS-Office computer skills.
- Ability to adapt to changing priorities and schedules.
- Willingness to continuously upgrade knowledge and education.
Experience
- Minimum 2-5 years of experience in the GMP-regulated industry.
