Gland Pharma Released Job Openings On 24/01/2022.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.
Vacancy Details:
Gland Pharma Recruiting M Pharm in Pharmaceutics/Pharmaceutical Technology Formulations Candidates with 1 – 6 years experience for Formulation Scientist Position.Complete Details for the Formulation Scientist as follows.
Important Details :
- Location : Hyderabad
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application: 24/01/2022
- 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
Related Job : Telephonic Interview At Eris Lifesciences – Interested candidates may send their updated CVs
Job Description/Skills Required
Gland Pharma is looking for experienced Research Associates in Injectables Formulation R&D for our unit based out of Dundigal – Hyderabad.
Job Responsibilities:
•To perform pre – formulation and formulation development trials using QbD approach and to develop a robust formulation.
•Interact with cross functionally across departments and ensure timely submission and approval of the assigned projects as per agreed work plan.
•Navigate the project technically and provide feasible technical solutions so as to develop a product recipe that can be successfully manufactured post approval.
•Conduct literature search and evaluate patent landscape for assigned project and work out the pathway for least time to effect successful submission.
•Planning and execution of lab scale batches and stability batches and documentation of the same in Lab Note Book.
•To ensure successful scale up / exhibit batches at plant.
•Preparation of protocol and report for trial batches and execution of the development study accordingly.
•Preparation of Development Study Report after receipt of COAs.
•Preparation of Stability protocol and charge stability batches as per the protocol.
•Compilation of stability data as per ICH guidelines.
•To co-ordinate with cross functional departments like ARD, RA, QA, Production for project / product related activity.
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