Executive - Quality Control

About Intas

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Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations. The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world.

Through its subsidiaries, the International presence of Intas includes the following countries : over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare. The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world.

Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA. Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare.

At Intas, our success is fundamentally built on the strength of our people. Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence. This approach ensures that every employee plays a meaningful role in driving both the company's growth and advancements in global healthcare.

Job Title : Executive - Quality Control

Job Requisitions No. : 15783

Job Description

Roles and Responsibilites

• Responsible for IPQC testing for Albumin and IVIG testing on routine batches.
• Preparation of DRS, Log book entry and related documentation to be make online.
• Support to prepare Albumin and IVIG drug substance and Drug product testing and its release with all documents.
• Handling of QC instrument as HPLC / GC for routine sample and other instrumentation maintenance.
• Preparation of STP / SOP / DRS for QC documentation on routine basis.
• Responsible for IPQC, DS, DP and stability sample testing on routine batches.
• Involved in Analytical method validation. 8. Handle the instrument and Equipment for routine use as well as calibration and qualification.
• Routine Document checking.
• QMS related activities.
• Additional task as allocated by HOD.

Relevant Skills / Industry Experience

HPLC

GC

Industry : Biotech / Parenteral / Injectable

Relevant professional / Educational background

M.Sc. - Biotechnology / Organic Chenistry

B. Pharm

Location :

Plasma Fractionation Unit, Ahm, GJ, IN, 382210

Travel : 0%

Life at Intas Pharmaceuticals

For over three decades, Intas has thrived due to the exceptional talent of its people. Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success. We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape.

Date : 5 Nov 2025

Skills Required

Hplc, Gc