Research Scientist

Fresenius Kabi; Gurugram District; On-site; INR 900,000 - 1,500,000; Full time

Job summary

Fresenius Kabi Gurugram invites a Research Scientist to join Analytical Development (Formulation). The candidate will analyze development and stability samples using HPLC and other techniques, and lead method development, validation, and transfer activities. A M.

Pharm with 2–6 years’ experience is preferred to ensure GLP-compliant documentation and robust analytical records. The role emphasizes instrument calibration, documentation, and support for investigations and continuous process

Qualifications

• M. Pharm degree required; 2–6 years of experience in pharmaceutical analysis.
• Hands-on experience with HPLC and troubleshooting.
• Experience in analytical method development, evaluation and optimization.
• Knowledge of method verification, validation and transfer.
• Calibrations and qualification of analytical instruments.
• Strong GLP documentation practices and record maintenance.
• Compliance with GLP and company quality standards.

Responsibilities

• Analyze development and stability samples using HPLC and other chemical analytic techniques.
• Perform analytical method development, evaluation and optimization.
• Execute method verification, validation and transfer activities per regulatory requirements.
• Conduct calibration and qualification of analytical instruments.
• Prepare and maintain analytical records, reports and technical documentation.
• Ensure compliance with GLP and company quality standards.
• Support laboratory investigations, troubleshooting and continuous improvement.

Skills

HPLC operation

Method development

Method validation

Method transfer

Stability analysis

Instrument calibration

GLP documentation

Analytical lab operations

Education

M. Pharm

Job description

Hiring: Research Scientist

Location: Gurugram
Department: Analytical Development(Formulation)
Qualification: M. Pharm
Experience: 2-6 Years

Key Responsibilities

Analyze development and stability samples using HPLC and other chemical analytical techniques.

Perform analytical method development, evaluation, and optimization.

Execute method verification, validation, and method transfer activities as per regulatory requirements.

Conduct calibration and qualification of analytical instruments.

Prepare and maintain analytical records, reports, and technical documentation.

Ensure compliance with GLP and company quality standards.

Support laboratory investigations, troubleshooting, and continuous improvement initiatives.

Required Technical Skills

Hands-on expertise in HPLC operation and troubleshooting

Experience in Method Development & Method Validation

Knowledge of Method Transfer and Verification

Experience in Stability Sample Analysis

Understanding of analytical instrument calibration

Strong knowledge of GLP documentation practices

Good understanding of pharmaceutical analytical laboratory operations

Desired Competencies

Excellent communication and interpersonal skills

Proactive and collaborative mindset

Strong analytical and problem-solving abilities

Adaptable and flexible approach to work

Detail-oriented with a strong focus on quality and compliance

Ability to manage multiple priorities in a fast-paced environment