The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global lifesciences company that discovers, develops, manufactures, and markets a broad range of healthcare therapies. The group employs over 23000 people worldwide and is driven by its mission to unlock new possibilities in life-sciences through quality healthcare solutions that impact lives.Â
- Vacancy details:
- Department:IPQA professional for our OSD manufacturing
- Experience: Â 3 to 7 year(s)
- Qualification:M.Pharma/B.Pharma
- Salary:₹ 4-9 Lacs P.A.
Job Description: Greeting from Zydus Pharmaceuticals Ltd!!!
Important Details :
- Location:Ahmedabad
- Post of date :14/10/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Greetings from Zydus Pharmaceuticals Ltd!!!
We are looking for IPQA professional for our OSD manufacturing facility for the below role.
Officer to Senior Executive – (IPQA ): B. Pharm / M. Pharm with 3 to 7 Years of relevant experience of IPQA in Oral Solid Dosage Manufacturing facilities. which Includes below roles and responsibilities
To perform batch/equipment/area Line clearance activity.
To monitor dispensing, manufacturing and engineering activities.
To sample at In process and finished product stages and sampling for engineering/validation batches.
To execute of cleaning verification and validation activities.
To investigate deviations, out of trend/out of specification results and market complaints.
To review equipment audit trails, alarms and to trend critical alarms with appropriate investigation and CAPA, if applicable.
To review of Batch Manufacturing Records and to perform batch release.
To ensure timely completion of CAPAs and to perform change control/CAPA effectiveness.
To ensure effective implementation of Continued Process Verification through on line trending and statistical evaluation of Critical Process Parameters (CPP) and Critical Quality Attributes (CQA)
To monitor and take forward manufacturing tech transfer activities
For all the positions, it is essential for candidates to have exposure in regulatory requirements of documentation and cGMP/GLP. The person should be specifically from OSD formulations.
Interested candidates Please share their resume at manan.hathi@zyduslife.com.
