Syngene Senior Research Associate Recruitment - Pharmaceuticals Science

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

Apply Online

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