QA Job at Intas | MSc Graduates Apply Now for the Chemistry Job
Are you looking for a rewarding QA job or chemistry job with strong growth potential in a global pharmaceutical organization? The Officer – QA role at Intas Career offers an excellent opportunity to work on qualification activities, regulatory submissions, and validation processes while contributing to high-quality standards in a world-class manufacturing environment.
About the Intas
Intas Pharmaceuticals is a globally recognized, innovation-driven pharmaceutical company committed to delivering high-quality, affordable medicines across more than 85 countries. With strong capabilities in R&D, biosimilars, manufacturing, and regulatory excellence, Intas maintains approvals from leading agencies, including the USFDA, MHRA, and EMA. The company’s integrated approach and rapid international expansion make it a trusted name in global healthcare. Intas fosters a collaborative, growth-oriented culture that encourages innovation and professional development, making it an excellent destination for individuals seeking a QA job, chemistry job, or long-term growth through Intas Career opportunities. Employees play a vital role in advancing impactful healthcare solutions worldwide.
Job Details
- Job Title: Officer – QA
- Job Requisitions No.: 13786
- Location: SEZ, Ahmedabad, GJ, IN, 382213
- Qualification Required: B. Pharm/ M. Pharm/ MSC.
- Skills / Industry experience
2 to 3 years of experience in a USFDA, MHRA, TGA-approved plant
Purpose of Job
Mr. Atul is working in Block H parenteral qualification activity. He is involved in qualification activities and regulatory summary submission activities.
Roles and Responsibilities
- Media fill and qualification summary preparation knowledge.
- To maintain track of qualification and validation activities.
- To prepare and review the protocols and reports. Execution of various qualification/validation activities.
- To review the correctness of the technical documents received from the supplier (DQ/OQ/IQ/PQ, FAT).
- Coordinate with production and other user departments for qualification/validation activities.
- Timely compilation and review of qualification validation reports.
- To review the equipment documents, like calibration reports, and ensure the correctness of the documents.
- To perform FAT.
- To coordinate with outside agencies for the execution of qualification activity whenever required.
- Identification of deviation through review and observation.
- To prepare the annual Re-qualification/validation schedule, update VMP and qualification-related SOPs as and when required.
