Syngene M Pharma SRA Syngene Hiring, M Pharma candoidates apply. Candidates with experince of 1 to 3 years in the filed of Pharmaceutical Development here’s a job awaiting for you with syngene. Intrested and eligible candidates may check out all the details on the same below:
Job Title: Senior Research Associate – Pharmaceutical Development (53682)
Eligbility Criteria: M Pharma
Experience: 1 – 3 years
Primary Responsibilities:
Project Planning
Ensure proper planning and availability of resources for seamless execution of projects.
Manage project related supplies of API, raw materials and packaging components as required.
Discuss with cross functional teams for project related activities
Project Execution and management
- Conduct literature search for research purposes
- Execute projects related to pre-formulation, formulation and process development, scale up, Technology transfer and cGMP manufacturing of oral solid products.
Plan and execute stability studies and stability protocol preparation - Ensure seamless execution of projects as per committed timelines.
- Troubleshooting and problem solving for challenges within projects
- Interact with cross functional teams for execution of projects.
- Effectively co-ordination between teams for cross functional activities.
- Execute GMP activities for manual filling of drug in capsule (Dic) and drug in bottle projects.
Documentation
- Ensure appropriate documentation for projects as per Syngene policy.
- Compilation and interpretation of results and report writing
- Manage laboratory notebook for all concerned projects. Compile and manage data and write protocols, reports as required.
- Preparation and review of Master formula records, Batch manufacturing records and Batch packaging records for execution of GMP batches.
Quality Compliance
Compliance and Adherence to all Syngene quality systems
EHS Compliance
Compliance to Syngene EHS policies and systems
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