SrResearch Associate – Discovery Chemistry | Bangalore | Syngene

Job Description

Job purpose:

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 Responsibilities:

Primary Responsibilities:

1. 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 notebook for all concerned projects. Compile and manage data and write protocols, and 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 with Syngene EHS policies and systems

Secondary Responsibilities:

1. Support for preparation of SOPs, EOPs, and IOPs.
2. Support for client visits and audits.

Educational Qualification & Experience: 

M Pharma with 3-6 years of experience