Zydus Lifesciences Limited Walk In Interview 2023.Zydus Lifesciences Limited Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue.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.
- DESIGNATION: Senior Executive to Dy. Manager – (IPQA )/ Oral Solid Dosage Manufacturing facilities
- Qualification: B. Pharm / M. Pharm
- Experienced:04 to 9 year(s) of experience
- Salary: 5-12 Lacs P.A.
Job Description: Greeting from Zydus Lifesciences Limited !!!!
Important Details :
- Location: Ahmedabad
- Post of date:19/03/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
- Interview Rounds of Interview: HR
We are looking for IPQA professional for the below role.
Senior Executive to Dy. Manager – (IPQA ): B. Pharm / M. Pharm with 4 to 10 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 email@example.com for further evaluation.