Quality Control Executive – Chemical Analyst

About this role

Role involves performing and reviewing chemical analyses of raw materials, in-process materials, intermediates, finished products and stability samples using approved methods and laboratory instruments. It requires familiarity with analytical software and maintaining records for HPLC and related usage. The position targets candidates with 5–8 years of quality control experience in chemical analysis within the pharmaceutical API or regulated chemical manufacturing sector.

What you would do

• Perform and review chemical analyses of materials and products using approved methods and laboratory instruments
• Maintain HPLC usage logs and related records, including mobile phase usage
• Verify and record usage of working standards, impurity standards and reference standards; manage vial destruction records
• Review analytical data from HPLC, GC, GC-HS, IR and UV and document outcomes
• Prepare certificates of analysis and assist in developing new analytical methods for HPLC, GC or GC-HS as required by MOA
• Oversee instrument qualification/validation, maintenance planning and SOP preparation; support QA activities

What they are asking for

• BSc or MSc in Chemistry, Industrial Chemistry, Pharmaceutical Chemistry or a related discipline
• 5–8 years of Quality Control experience in chemical analysis within the pharmaceutical API or regulated chemical manufacturing industry
• Technical competencies in chemical analysis and instruments (HPLC, GC, GC-HS, UV); knowledge of cGLP, data integrity and laboratory documentation

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