Senior Research Scientist

Macsen Laboratories; Udaipur District; On-site; INR 420,000 - 640,000; Full time

Job summary

Macsen Laboratories seeks a qualified analytical chemist to support pharmaceutical analysis and method development. You will handle chromatographic instrumentation (HPLC, GC, LC-MS) and perform critical analysis of R&D and QA samples, ensuring accuracy and compliance.

The role requires hands-on experience with instrument operation, method validation, SOPs, and GMP practices, with strong documentation and autonomy in daily lab activities.

Qualifications

• Experience in preparation of volumetric solutions and reagents.
• Knowledge of GMP/lab safety and PPE.
• Familiarity with SOPs and documentation.
• Ability to troubleshoot sophisticated instruments.

Responsibilities

• Prepare volumetric solutions, mobile phase, and reagents.
• Hand-hold operation of instruments HPLC/GC/LC-MS.
• Apply good chromatographic practices and troubleshoot instruments.
• Engage in method development and validation, instrumental analysis.
• Manage stability and shelf-life studies for products.
• Analyze samples from R&D (Synthesis) including in-process monitoring.
• Prepare/review SOPs, protocols, and ARD documentation.
• Manage reagents and consumables requirements.
• Know regulatory guidelines relevant to the work.
• Work independently and handle lab operations when needed.
• Maintain lab records and GMP-compliant logbooks.
• Handle chemicals and samples with appropriate PPE and safety norms.

Skills

Chromatography

Instrument handling

Documentation

Education

Bachelor's degree in Chemistry or Analytical Chemistry

Tools

HPLC

GC

LC-MS

Job description

Role & responsibilities

1. Expertization on Preparation of Volumetric solution, Mobile phase, and Reagent.
2. Familiar with hand-holding for operation and handling of the latest laboratory instruments, Apparatus, and software (HPLC/GC/LCMS/GCMS, etc.)
3. Working Knowledge of Good chromatographic practices and Troubleshooting related to sophisticated instruments like HPLC/GC, etc.
4. Sound knowledge of Method development & Method validation, instrumental method of analysis, and logical approach.
5. Manage Stability & shelf-life Studies for new product /existing product as and when required.
6. Analysis of samples received from R&D (Synthesis) (Samples include in-process Reaction monitoring, intermediate, finished product.
7. Responsible for the preparation and review of SOPS, protocol, Reports and relevant documentation of ARD.
8. Manage all reagent and consumable Requirements.
9. Knowledge of Different regulatory guidelines.
10. Capable of working independently and handling laboratory operations if required.
11. Maintain lab records and logbooks according to GMP.
12. Familiar with handling chemicals, pharmaceutical product samples, and aware of laboratory safety norms and PPE usage.

Preferred candidate profil:

Experience in handling instruments like HPLC, GC, and LC-MS.