Cadila Pharmaceuticals

Perform chemical analysis of APIs, intermediates, and raw materials as per approved specifications and SOPs. Handle and review analytical testing using HPLC, GC, UV, FTIR, KF, pH, and other QC instru

"To maintain proper hygienic condition before entering to manufacturing area To follow manufacturing area entry exit procedure properly. To take part in training whenever necessary. Preparation of

•To maintain proper hygienic condition before entering to manufacturing area •To follow packing area entry exit procedure properly. •To take part in training whenever necessary. •To check and ensur

1. Planning and execution of Validation, Qualification, Re-Qualification and Re-Validation activities pertaining to Manufacturing facility at Dholka site in line with the cGMP requirements of national

To maintain proper hygienic condition before entering to parenteral manufacturing area. To follow parenteral manufacturing area entry exit procedure properly. To take part in training whenever neces

1. Ensure compliance with cGMP requirements, Good Engineering Practices (GEP), and all applicable statutory laws, rules, and regulations. 2. Carry out operation and maintenance activities related to

• Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of raw material on non-chromatographic instrument such as FTIR, UV, Polarimeter, KF, Autotitrator etc. by following tes

To ensure proper hygienic condition of workmen before entering to packing area. To ensure packing area entry exit procedure is properly followed by workmen. To ensure packing area equipment are oper

JOB RESPONSIBILITIES 1. Working on Unit operations related toupstream processing during Drug Substance (DS) manufacturing. 2. GMP documentation related to DS manufacturing like batch records, equip

Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process condi