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Senior Research Associate - Pharmaceutical Development

1.00 to 3.00 Years   Delhi   10 Apr, 2023
Syngene International Limited
Job LocationDelhi
EducationNot Mentioned
SalaryNot Disclosed
IndustryEducation / Training
Functional AreaBio Tech / R&D / Scientist
EmploymentTypeFull-time

Job Description

    • 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 ComplianceCompliance and Adherence to all Syngene quality systemsEHS ComplianceCompliance to Syngene EHS policies and systemsEducational Qualification: M PharmaExperience: 1 - 3 years,

Keyskills :
researchvalidationhplcnmrliteratureequal employment opportunityanimal healthdata managementcgmp manufacturing

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