About Intas

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Intas Pharmaceuticals does not request or accept any fees during recruitment. If someone asks for payment on our behalf, it is a scam. Please report the incident to the local police or cybercrime unit. Your trust and safety are important to us.

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.:  13819
Job Description: 

Purpose of Job

Responsible for handling Instrumental analysis of all products ,Planning, Documentation, Method
Validation, Instrument Calibration / Verification.

Skill Required

-Analysis of samples for batch release, stability testing, comparative analysis, validation and
other testing activities along with proper documentation as per approved STPs and approved
protocols.
-Support in investigation of Deviation, LIR, OOS or OOT. 

-Preparation and revision of documents as & when required

Roles and Responsibilites

-Participate in training/ qualification/ validation of methods during technology transfer from R&D
to QC as per schedule and to complete related documentation timely.

-Perform verification/ calibration/ qualification/ monitoring activities of various QC instruments/
equipments as per schedule.-To support in internal as well as external audit compliance. 

-Responsible for general work place cleanliness, safety compliance, equipment management
and adherence to all approved SOPs and GMP procedures.

-Any other responsibility assigned by the supervisor.

-To follow ‘Good Documentation Practices and Data Integrity’ requirements during any GxP
Operation and recording at site.

-To take responsibility that application of Data Integrity requirements and potential
consequences for not following it are understood and followed

Qualification Required

M.Sc/M.Tech - Biotechnology & Analitical Chemistry

Relevant skills / Industry experience

Relevant professional / Educational background

Any other requirements (If any)

Compensation / Reward

Location: 

Biotech, Ahmedabad, GJ, IN, 382213

Travel:  0% - 25%

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:  26 May 2025