Senior Executive, Quality Control (QCC)

2 - 7 years

0 Lacs

Posted:1 day ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

You will be responsible for testing and releasing raw material, packing material, and miscellaneous material samples. You must maintain reserve samples as per standard operating procedures (SOP). Your role will involve preparing specifications of raw materials, packing material, in-process and finished products, and stability protocols as required. You will also be responsible for preparing study protocols for the laboratory. Your key responsibilities will include: - Sampling raw material, packing material, and miscellaneous material samples and maintaining reserve samples as per SOP - Preparing volumetric solutions, reagent solutions, working standards, and maintaining records - Performing water analysis according to specifications, SOP, and GTP - Maintaining daily water analysis trend records - Preparing and maintaining laboratory reagents and volumetric solutions as per SOP - Ensuring workplace cleanliness and following good laboratory practices - Testing and releasing in-process, finished products, standards, and stability samples - Updating instrument logbooks and recording data in the Laboratory Notebook during testing - Performing calibration and maintenance of all instruments/equipment as per schedule Additionally, as part of the QC department of a sterile manufacturing plant, you must have a Bachelor of Science (B.Sc.), Master of Science (M.Sc.), or Bachelor of Pharmacy (B.Pharma) degree with 2-7 years of experience. Candidates applying for internal jobs should have completed at least 2 years within their existing role. Please note that the company values training and development. You will be responsible for training new employees, sharing login credentials, updating training records, and ensuring employees are trained as per function mapping before work. As the Department training coordinator (DTC) for the QCC Department, you will oversee training-related activities, including initiating AIMS requisitions, preparing and reviewing QC-related SOPs, and handling general test procedures. In summary, you will play a crucial role in the quality control department by ensuring compliance with SOPs, maintaining accurate records, and contributing to the overall efficiency of the laboratory operations.,

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Amneal Pharmaceuticals logo
Amneal Pharmaceuticals

Pharmaceutical Manufacturing

Bridgewater New Jersey

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