Pharma & Chemistry Analyst Post Vacancy @ Cipla Ltd

Exclusive Job Opportunity for Pharma and Chemistry candidates. Cipla Ltd has announced the recruitment of Msc Chemistry M Pharma & B Pharma experience candidates. Msc Chemistry jobs at Cipla Ltd. Pharmacy jobs @ Cipla Ltd. Cipla Ltd hiring undergraduates and postgraduates Pharma candidates for the post of analyst. Check out all the details on the same below:

Job Title: FORMULATION ADL ANALYST – LCMS / GCMS

Work Location: Mumbai

Eligibility:

B.Sc – Chemistry, B.Pharma – Pharmacy, MS/M.Sc(Science) – Any Specialization, Chemistry, M.Pharma – Pharmacy

Experience: 1 to 5 years

Job Description:

  • Perform part method validation, forced degradation studies, excipient compatibility studies, reverse engineering, add-mixture studies, in-use studies, hold-time study and analysis of routine & stability studies
  • Conduct cleaning validation studies
  • Perform analysis of API, excipients and secondary material (packaging material, ink, adhesive etc.)
  • Develop cost effective & time saving analytical method for new or existing product
  • Evaluate the pharmacopeia and verify the documents
  • Maintain the lab instruments / equipment and troubleshoot the issues
  • Perform calibration (schedule / breakdown) and calculate instrument utilization
  • Up-keep the HPLC/GC/IC/LCMS/GCMS columns as per cGLP
  • Record and document all analytical activities in timely manner in ELN, instrument/equipment and column log book
  • Provide base documents for MOA / COA preparation for better coordination in analytical studies
  • Transfer methods and technologies to other units and departments
  • Study the literature to resolve units and regulatory queries and conduct investigation studies in stipulated time period
  • Analyse samples at pilot plant and unit for trace determination (Cleaning Validation)
  • Follow safety guidelines by ensuring use of PPE & MSDS of chemicals at time of analysis
  • Upkeep the samples given for analysis and ensure timely destruction after analysis as per SOP
  • Dispose solvents and waste generated during the analysis
  • Arrange analytical requirements like column, impurities, standards, placebo and samples for units and other department like Validation Lab or Outsourced Lab
  • Review and recommend corrections in the MOA, COA & Specifications

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