Lead Research Scientist - Technology transfer
Apotex Inc.
Full time- 6+ years
- Not Disclosed
- Bengaluru, India
- Post Date: Jun 19, 2026
- End Date: Aug 19, 2026
- 6+ years
- Not Disclosed
- Bengaluru, India
- Post Date:Jun 19, 2026
- End Date: Aug 19, 2026
Skills:
- pharma
- Quality control
- Management
Job Description:
Responsibilities
- Responsible for tech-transfer of injectable and ophthalmic formulations from R&D to commercial scale
- Gap analysis - To evaluate the product feasibility, technology feasibility at manufacturing site along with gap analysis with available technology for site readiness
- Documentation – Onsite documentation, and timely execution of scaleup, exhibit and validation batches
- Risk assessment – To carry out the risk assessment to identify the impact of critical process parameters and critical material attributes
- To design and review the sampling plan for scaleup, process optimization and submission batches
- To study and verify the parameters established during development are still with in the determined design space in scaleup and exhibit batches
- To coordinate with other departments at plant in completing scaleup and exhibit batch related activities
- In coordination with CMO and PM, ensure the availability of raw materials, packaging materials, filters, tubings etc. required for scale-up, exhibit and commercial batches before initiation of execution
- Compile the batch orsevations and prepare the report of scale-up, EB and commercial/PV batches
- To ensure smooth technology transfer of products developed at Apotex to CMO
- Technical support to formulation development team
- Involve in formulation development activities and assist in development of scaleable manufacturing process
- Review and compilation of the developmental plant scale batches data and stability results
- Coordination with different cross-functional teams like AD, procurement, QA, packing, regulatory affairs, project management for smooth execution of scale-up batches
- Coordination with external labs for successful completion and receipt of studies data performed for plant scale batches
- Review of MFR, BMR, BPR, stability protocols, study protocols and reports, Executed BMR, BPR,
- Issuance, maintenance, writing, review of raw data, completeness check and archival of laboratory notebook
- Coordination with vendor and internal service engineer for installation, calibration, maintenance and trouble shooting
- Report to next level manager regarding day to day activities.
- Preparation of SOPs and ensure compliance as per SOP
- Take up any other work as allotted
Qualification & Experience
- D /M Pharma in Pharmaceutics/B.Pharma.
- Knowledge, Skills and Abilities
- Must have experience in development and tech-transfer of injectable and ophthalmic and complex drug products
- Effective command over verbal and written communication with good interpersonnel skills.
- Engage with CMO partners and support the group submission plans
- Proficient in MS office and advanced software tools.
- Having well versed knowledge on regulatory guidelines
- Able to priortise the task, best in effective planning of work activities to meet the timelines.
- Experience
- Minimum 6 to 10+ years of experience in Injectable and Ophthalmic dosage forms in area of Development, Manufacturing and technology transfer expertise for CMO.
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Salary
Not Disclosed
-
Role
Executive or Officer
-
Area of Practice
- Quality Assurance/ Quality Control
- Clinical Operations
-
Experience
6+ years
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