Project Associate

Fresenius Kabi

Gurugram District

On-site

INR 350,000 - 520,000

Part time

14 days+

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Job summary

Fresenius Kabi Oncology Ltd. in Gurugram is hiring a Project Associate Formulation Development to join our pharma development team.

This 1-year contract role requires M.Pharm qualifications and up to 1 year of experience in formulation development, with a focus on injectable formulations for global markets. The position is based 100% in-office at Sector 32, Gurugram, offering hands-on development work, QbD-driven design, technology transfer activities, and strong compliance with regulatory

Qualifications

  • M.Pharm (Pharmaceutics) or M.Pharm (Industrial Pharmacy) degree.
  • 0–1 year of experience in formulation development.
  • Experience with injectable formulations is a plus.

Responsibilities

  • Develop injectable formulations (Cytotoxic & Non-Cytotoxic) for global markets.
  • Design and optimize liquid and complex injectable formulations.
  • Apply Quality by Design (QbD) principles during formulation development.
  • Prepare and support Technology Transfer documentation and plant transfer activities.
  • Contribute to laboratory maintenance and documentation.
  • Ensure compliance with applicable regulatory and quality standards.

Education

M.Pharm (Pharmaceutics)
M.Pharm (Industrial Pharmacy)

Job description

WE ARE HIRING

Project Associate Formulation Development

Fresenius Kabi Oncology Ltd.


Location: Sector 32, Gurugram

Qualification

  • M.Pharm (Pharmaceutics)
  • M.Pharm (Industrial Pharmacy)

Experience
0–1 Years in Formulation Development


Work Mode
100% Work from Office

Employment Type
1-Year Contract

Key Responsibilities

Develop injectable formulations (Cytotoxic & Non-Cytotoxic) for global markets.

Design and optimize liquid and complex injectable formulations.

Apply Quality by Design (QbD) principles during formulation development.

Prepare and support Technology Transfer documentation and plant transfer activities.

Contribute to laboratory maintenance and documentation.

Ensure compliance with applicable regulatory and quality standards.


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