QC Chemicals

2 weeks ago

india Job Excel Full time
Job Description
  • Ensuring the quality and compliance of our pharmaceutical products, including those in formulation, through rigorous chemical analysis and testing. You will be responsible for overseeing and executing quality control activities related to the chemical aspects of product manufacturing, ensuring adherence to regulatory standards and company policies.
  • Performing a wide range of chemical tests and analyses on raw materials, intermediates, finished products, and formulation samples using various analytical techniques, such as HPLC, GC, FTIR, UV-Vis spectroscopy, and wet chemistry methods.
  • To improve analytical techniques, enhance sensitivity, and reduce analysis time and costs, with a focus on formulation testing.
  • Ensure all quality control activities comply with current Good Manufacturing Practice (cGMP), Good Laboratory Practice (GLP), and other relevant regulatory standards, including those applicable to formulation testing.
  • Maintain accurate and complete documentation of all testing procedures, results, and records in compliance with regulatory requirements and company policies, particularly for formulation samples.

Requirements
  • Previous experience working in a pharmaceutical quality control environment is essential, with a strong background in chemical analysis and testing techniques.
  • Proficiency in operating and troubleshooting analytical instruments and equipment, with hands-on experience in HPLC, GC, FTIR, UV-Vis spectroscopy, and other relevant technologies.
  • Knowledge of analytical chemistry principles, including qualitative and quantitative analysis, formulation analysis, separation techniques, and spectroscopic methods.
  • Familiarity with laboratory information management systems (LIMS), data analysis software, and electronic laboratory notebooks (ELN) is beneficial.
  • Understanding of current Good Manufacturing Practice (cGMP), Good Laboratory Practice (GLP), International Council for Harmonization (ICH) guidelines, and other relevant regulatory requirements
  • Strong analytical and problem-solving abilities, the ability to maintain accurate and complete records of testing procedures, results, and documentation in compliance with regulatory standards and company policies.
  • Excellent verbal and written communication skills to convey technical information effectively, collaborate with cross-functional teams.

Requirements
Previous experience working in a pharmaceutical quality control environment is essential, with a strong background in chemical analysis and testing techniques. Proficiency in operating and troubleshooting analytical instruments and equipment, with hands-on experience in HPLC, GC, FTIR, UV-Vis spectroscopy, and other relevant technologies. Knowledge of analytical chemistry principles, including qualitative and quantitative analysis, formulation analysis, separation techniques, and spectroscopic methods. Familiarity with laboratory information management systems (LIMS), data analysis software, and electronic laboratory notebooks (ELN) is beneficial. Understanding of current Good Manufacturing Practice (cGMP), Good Laboratory Practice (GLP), International Council for Harmonization (ICH) guidelines, and other relevant regulatory requirements Strong analytical and problem-solving abilities, the ability to maintain accurate and complete records of testing procedures, results, and documentation in compliance with regulatory standards and company policies. Excellent verbal and written communication skills to convey technical information effectively, collaborate with cross-functional teams.

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