Chemveda Life Sciences Walk-in Interview.Chemveda Life Sciences Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Position Name: Research Chemist/Senior Research Chemist/Research Associate
- Experience: 1 to 5 years
- Qualification: M.Sc Analytical Chemistry/Organic Chemistry/M.pharm
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
We are conducting walk-in drive on 05th July (Saturday) 2025 for the positions in our Analytical Research & Development department.
Job Description:
Work location:ย 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,Hyderabad
Key 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 toย saivardhan.kothuri@chemvedals.com