Walk -in Drive For AR&D positions - HPLC,LCMS & Wet Analysis

Dear Candidate,

We are conducting walk-in drive on 05th July (Saturday) 2025 for the positions in our Analytical Research & Development department.

Position Name:

Experience:

Qualification:

Work location:

Walk-in Date: 05th July 2025 (Saturday)

Time: 09:00 AM to 12.00 PM

High-Performance Liquid Chromatography (HPLC)

Key Skills and Competencies:

• Operation and Maintenance

  : Proficiency in operating HPLC systems (e.g., Agilent, Waters, Shimadzu) and performing routine maintenance, calibration, and troubleshooting of equipment issues like pressure fluctuations or detector errors.

• Method Development and Validation

  : Ability to develop and optimize HPLC methods for analyzing small molecules, impurities, or degradation products, adhering to ICH guidelines (e.g., ICH Q2 for validation).

• Data Analysis

  : Expertise in interpreting chromatograms, quantifying analytes, and using software like Empower or ChemStation for data processing and reporting.

• Sample Preparation

  : Skilled in preparing samples (e.g., dissolution, extraction) for pharmaceutical or chemical analysis, ensuring reproducibility and accuracy.

• Regulatory Compliance

  : Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) for documentation, method validation, and audit readiness.

• Troubleshooting

  : Ability to diagnose and resolve issues such as peak tailing, baseline drift, or column degradation.

Experience Level (1-5 Years)

• 1-2 years: Basic operation, routine analysis, and data interpretation under supervision.
• 3-5 years: Independent method development, validation, and troubleshooting with familiarity in handling complex matrices.

2. Wet Analysis in Good Laboratory Practices (GLP)

Key Skills and Competencies:

• Classical Analytical Techniques

  : Proficiency in titration (acid-base, redox, complexometric), gravimetric analysis, and other wet chemistry techniques for assay determination or impurity profiling.

• GLP Compliance

  : Strict adherence to GLP standards, including proper documentation, sample tracking, and maintaining a chain of custody for regulatory audits.

• Standard Operating Procedures (SOPs)

  : Ability to follow and draft SOPs for wet analysis methods, ensuring consistency and compliance.

• Quality Control

  : Knowledge of preparing and standardizing reagents, performing limit tests, and ensuring accuracy in quantitative and qualitative analysis.

• Safety and Handling

  : Expertise in safe handling of chemicals, waste disposal, and maintaining a contamination-free lab environment.

• Data Integrity

  : Ensuring accurate record-keeping, traceability, and error-free reporting in lab notebooks or electronic systems.

Experience Level (1-2 Years)

• 1-2 years: Performing routine titrations, standardization, and sample preparation under GLP guidelines.

3. Liquid Chromatography-Mass Spectrometry (LCMS)

Key Skills and Competencies:

• Instrument Operation

  : Proficiency in operating LCMS systems (e.g., Thermo Fisher, AB Sciex) for qualitative and quantitative analysis, including single quadrupole, triple quadrupole, or high-resolution MS (e.g., Orbitrap).

• Method Development

  : Ability to develop LCMS methods for identifying and quantifying trace-level impurities, metabolites, or active pharmaceutical ingredients (APIs) in complex matrices.

• Mass Spectra Interpretation

  : Expertise in analyzing mass spectra, identifying molecular ions, adducts, and fragmentation patterns for structural elucidation.

• Sample Preparation

  : Skilled in sample extraction techniques (e.g., SPE, LLE) and matrix effect minimization for bioanalytical or pharmaceutical samples.

• Software Proficiency

  : Familiarity with LCMS software (e.g., Xcalibur, Analyst) for data acquisition, processing, and reporting.

• Regulatory Knowledge

  : Understanding of regulatory requirements (e.g., FDA, EMA, ICH) for bioanalytical method validation and GLP/GMP compliance.

• Troubleshooting

  : Ability to address issues like ion suppression, carryover, or instrument sensitivity.

Experience Level (1-5 Years)

• 1-2 years: Conducting routine LCMS analysis, sample preparation, and basic data interpretation under guidance.
• 3-5 years: Independently developing and validating LCMS methods, troubleshooting complex issues, and supporting drug discovery or development projects.

Interested candidates can attend walk-in drive or share their profiles to