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Walk -in Drive For Ar&d Positions - Hplc,lcms & Wet Analysis @ Chemveda Life Sciences

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Chemveda Life Sciences  Walk -in Drive For Ar&d Positions - Hplc,lcms & Wet Analysis

Job Description

Dear Candidate,


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


Job Description:


Position Name: Research Chemist/Senior Research Chemist/Research Associate

Experience: 1 to 5 years

Qualification: M.Sc Analytical Chemistry/Organic Chemistry/M.pharm

Work location: Uppal/Mallapur


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

Time: 09:00 AM to 12.00 PM
Venue:-Plot No. B-11/1,,,IDA Uppal,HyderabadKey Skills and Competencies:

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 sa***************i@ch*******s.com

Job Classification

Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Research & Development
Role Category: Research & Development - Other
Role: Research & Development - Other
Employement Type: Walk-ins

Contact Details:

Company: Chemveda Life Sciences
Location(s): Mallapur

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Keyskills:   AR&D HPLC LCMS Wet Analysis

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Chemveda Life Sciences

Chemveda Life Sciences is a mid-sized, rapid-growing solution provider to the pharmaceutical, biotech, academia, and agrochemical industries. As a contract research partner Chemveda is boosting its value creation along and beyond the drug discovery & development continuum with a strong focus on ...