Intas Pharmaceuticals walk in interview for Quality Control Professionals

Intas Pharmaceuticals Hiring Quality Control Professionals: Shape Your Career with Excellence!
About the Company
Welcome to Intas Pharmaceuticals, a global leader in pharmaceutical formulation development, manufacturing, and marketing. With a presence in over 85 countries and a remarkable 20% CAGR growth, Intas contributes to a world of good health, happiness, and hope. Join us in our mission to make a difference every day.
Company Vacancies List
Position Titles:
- Assistant Manager
- Department: Quality Control
- Section: QC-Shift In Charge
- Qualification: M.Sc/B.Pharm/M.Pharm
- Experience: 12 to 16 Yrs
- Responsibilities:
- Resource Allocation and Work Schedule Planning
- Reduction of unconfirmed OOS/OOT
- Exposure to CDS and Non-CDS (Chromatographic Database Software)
- Worked in USFDA/MHRA/EU certified labs
- Exposure to Dl and DG
- Handling a team size of 10 to 15 employees
- Exposure to Formulations like Solid, Injectable, Onco Product, etc.
- Senior Executive
- Department: Quality Control
- Section: QC-Supervisor
- Qualification: B.Sc/M.Sc/B.Pharmacy/M.Pharm
- Experience: 07 to 12 Yrs
- Responsibilities:
- Verify sequence before the start of analysis
- Control human error
- Troubleshoot instruments & method techniques
- Reduction of unconfirmed OOS/OOT
- Review calibration & qualification activities of QC testing
- Officer to Senior Executive
- Department: Quality Control
- Section: QC-FG/Stability/AMV
- Qualification: B.Sc/M.Sc/B.Pharmacy/M.Pharm
- Experience: 02 to 08 Yrs
- Responsibilities:
- Work in Finished Goods & Stability Section
- Knowledge of Instruments HPLC/GC
- Preferably know-how of Chromeleon Software
Note: Carry your updated resume, educational credentials, and salary documents to the interview.

Job Description
About the Department & Responsibilities
At Intas, the Quality Control department plays a crucial role in ensuring the highest standards. Depending on the position, your responsibilities may include:
- Supervision of granulation, compression, or FG/Stability/AMV sections
- Verification of sequence and troubleshooting in analysis
- Handling various formulation processes like Solid, Injectable, Onco Product, etc.
- Compliance with regulatory standards such as USFDA, MHRA, and EU
- Reviewing calibration & qualification activities in QC testing
- Shift duties and the flexibility to work in a regulated plant environment
How to Apply
Join us for a walk-in drive on 17 November 2023 (Friday) between 09:00 am to 05:00 pm at Intas Pharmez, Ahmedabad. The venue details are as follows:
Venue: Intas Pharmaceutical Limited, Plot No 5 to 14, Pharmez Sarkhej Bavla Highway, At & Po: Motoda. Ta Sanad Dist: Ahmedabad-328 210.
Note: Intas Pharmaceuticals Ltd. does not charge any fee for job applications, processing, training, or any related activities.