Gland Pharma Released Job Openings On 12/07/2022.A holistic objective of dispensing health through a portfolio of injectable products across various therapeutic segments and delivery systems, has helped us expand to seven manufacturing facilities in India, with a capacity of approximately 750 million units. Â
Vacancy Details:
Gland Pharma Recruiting B.Pharma Candidates with 01-06 years experience for Associate/ Senior Associate -Technology Transfer Position.Complete Details for the Associate/ Senior Associate -Technology Transfer as follows.
Important Details :
- Location : Hyderabad/Secunderabad
- No of Vacancies:02
- Details of Salary:NA
- Opening date for online Application: 12/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
Facilitate the Technology transfer from R&D to manufacturing plant / Site Transfer.
Coordinate TT Activities across site functions with IPD cross functional teams and manufacturing unit team for successful execution of projects as assigned by technology transfer head.
For the successful new product Launch and implement the Execution Plan at the Site following activities to be performed/Ensured:
Gap Assessment
Plant Readiness Assessment / Execution
Batch Execution & Qualification
Appropriate Documentation & Records
Review and Assessment for QTPP, CQA CME, Trade dress, RA strategy.
Review of sterilizing grade filter validation documents.
Procurement of Raw material, Packaging material, Filters, silicon tubes and consumables with Co-ordination with R&D, SCM required for forthcoming projects.
To ensure availability of tooling, change parts, materials, equipments required for execution of new products feasibility/ assessment/ registration batches at unit.Initiation of Change controls for introduction of new product to facility.
Execution and monitoring of QbD batches for optimization of critical process parameter through Lab note book. On basis of Qbd batch results preparation of control strategy for Scale-up and Exhibit.
Review of sampling protocols for QbD and scale-up batches and compilation of scale-up reports.
Execution and monitoring Scale-up, Exhibit, and Process validation batches.
Designing and review of Master Formula card and Master Batch Manufacturing Records (BMR).
To coordinate with R&D/ F&D to passes all relevant quality product details, technical documents, regulatory requirements and logistic information to the receiving unit.
To ensure all required documents are provided to RA from unit QA on time for filing. Review and approve the Master documents required for the execution of new products transfer. Perform review and approval of change control for Feasibility, Assessment and Registration batches.
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