ADL Executive

Job highlights

• Maintain proper documentation of test results,certificates of analysis (CoA),batch records,and specifications

• Ensure compliance with Good Laboratory Practices (GLP) and industry standards

• . Hands-on experience with analytical instruments (HPLC,GC,UV,FTIR,Dissolution)

• Conduct HPLC, GC, UV Spectroscopy, FTIR, Dissolution, and other analytical tests as per standard operating procedures (SOPs).

• Develop and validate analytical methods for raw materials, intermediates, drug substances, and finished products.

• Ensure methods are suitable for quality control, stability studies, and regulatory submissions.

• Analysis of formulation, API, and stability. (In-process / Intermediate / BU / CU / Assay / Dissolution / RS)

• Ensure compliance with Good Laboratory Practices (GLP) and industry standards.

• Conduct stability studies as per ICH guidelines and prepare related reports.

• Maintain proper documentation of test results, certificates of analysis (CoA), batch records, and specifications.

• Ensure compliance with GMP, WHO, USFDA, MHRA, EU-GMP, and other regulatory guidelines.

• Participate in internal and external audits and assist in audit preparations.

• Conduct periodic calibration and validation of laboratory instruments.

• Hands-on experience with analytical instruments (HPLC, GC, UV, FTIR, Dissolution).

• Knowledge of pharmacopoeial guidelines (USP, BP, EP).