Syngene Senior Research Associate Recruitment – Pharmaceuticals
Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing services company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical sectors. Syngene’s 4500+ scientists offer both skills and the capacity to deliver great science
Job Title: Senior Research Associate, Pharmaceutical Development
This job is no longer accepting applications
Job Location: Bengaluru, India
Reporting to: Team Leader, Pharmaceutical Development
Job Grade: 9
Eligibility Criteria: Master’s degree in Pharmaceuticals
Industry Experience 1-3 years of relevant experience
- Other competencies required for the role
- Support for preparation of SOPs, EOPs, IOPs.
- Support for client visits and audits.
- Operating Unit: Pharmaceutical Development
Department: Pharmaceutical Development
The Role
Responsible for pre-formulation and formulation development, stability studies, scale-up, and GMP manufacturing of drug products based on the scope of projects. Knowledge expected in terms of complex generic or NCE products which include but are not limited to microspheres/ nanoemulsion/ liposomes.
Key Result Areas
Role-specific:
Primary Responsibilities:
Project Execution and management (Knowledge expected in terms of complex generic or NCE products which include but not limited to microspheres/ nanoemulsion/ liposomes)
• Conduct literature search for research purposes
• Execute projects
related to pre-formulation, formulation, and process development, scale-up, Technology transfer, and cGMP manufacturing of clinical supplies.• Plan and execute stability studies and stability protocol preparation
• Ensure seamless execution of projects as per committed timelines.
Documentation
• Ensure appropriate documentation for projects as per Syngene policy.
• Compilation and interpretation of results and report writing
• Manage laboratory notebooks 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 the 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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