Avisa Pharma Advanced Research Centre

R&D Chemist – Quality Control Department

Role Overview: We are looking for a dedicated R&D Chemist to join our Quality Control Department. The role primarily involves conducting analytical testing and ensuring compliance with quality standards. The ideal candidate will have experience in quality control procedures and possess strong analytical skills.

Key Responsibilities:

  1. Perform analytical testing of raw materials, intermediates, and finished products using various techniques such as HPLC, GC, UV-Vis spectroscopy, and wet chemistry methods.
  2. Execute method validation and method transfer activities in accordance with regulatory requirements.
  3. Investigate out-of-specification results and deviations, and propose corrective and preventive actions.
  4. Participate in stability studies to assess the shelf-life and quality attributes of products.
  5. Maintain laboratory instruments and equipment, and troubleshoot technical issues as needed.
  6. Ensure compliance with Good Laboratory Practices (GLP) and other relevant regulatory guidelines.
  7. Document and report analytical data accurately and timely.

Qualifications:

  • Bachelor’s or Master’s degree in Chemistry.
  • For freshers: BSc in Chemistry or related field. For experienced candidates: MSc in Chemistry or related field.
  • 1-2 years of experience in a quality control laboratory, preferably in the pharmaceutical industry.
  • Familiarity with analytical techniques such as HPLC, GC, and spectroscopy.
  • Strong attention to detail and ability to work independently as well as part of a team.

Note: Candidates with relevant experience in quality control are encouraged to apply for the R&D Chemist position in the Quality Control Department.

Job Type: Full Time
Job Location: Por

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