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Zydus Lifesciences is seeking a QA professional for the Ahmedabad, Gujarat site to support sterile injectable manufacturing. Responsibilities include equipment qualification, validation, and process improvements, along with machine setup and startup activities.
The role requires a B. Pharm/M. Pharm and 2–4 years of relevant experience, with hands-on exposure to sterile manufacturing facilities. The team advocates a culture of innovation and quality in pharma operations.
Zhl-manufacturing Formulation|z For.mfg-vatva, Ahmedabad, Gujarat, India
Participate in equipment qualification,validation, and process improvement activities.
Participate in machine setup and startupactivities.
Ensuring implementation of Correctiveactions/Preventive actions.
Responsible for approving impact & riskassessment, URS, DQ, FAT, IQ, OQ, PQ documents for equipment’s/instrumentsand utilities.
Perform in-process quality assurance duringmanufacturing, filling and sealing of products.
To ensure compliance to cGMP in manufacturingfacility.
Requirements:
Qualification
B. Pharm/M. Pharm
Years of Experience
2 to 4 years
Experience in Zydus
1 to 2 years
Experience/ Exposure:
Must possess hands-on experience in SterileInjectable Manufacturing Plants
Job Snapshot
Updated Date
19-09-2026
Job ID
JOB11126
Division
ZHL LYOPHOLISE PLANT QA
Location
Location Zhl-manufacturing Formulation|z For.mfg-vatva, Ahmedabad, Gujarat, India
At Zydus Lifesciences, w e nurture a culture of innovation, excellence, and inclusivity , driving meaningful advancement in the pharmaceutical and healthcare industries. Fueled by creativity , we constantly exploring new ways to improve patient care and expand healthcare accessibility.
Our commitment to a positive and empowering work environment has earned us recognition as one of India's Best Workplaces in Biotechnology & Pharmaceuticals.