Zydus Pharmaceutical Ltd, 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. The group aspires to become a global life-sciences company transforming lives through pathbreaking discoveries. The group has manufacturing sites and research facilities spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim in India and in the US and Brazil.
Greetings from Zydus Pharmaceutical Ltd!!!
We are looking for QC Analyst for Greenfield OSD Facility based out of Ahmedabad and below are the details for your reference.
- Executive / Sr. Executive – (Analyst) B.Sc. /B. Pharm/M.Sc. with 4 to 7 years hands-on experience on analytical instruments like HPLC, GC, Dissolution apparatus, UV Visible Spectrometer.
- Candidate should also have exposure of wet Analysis, Stability Studies, for Oral Solid Dosage.
- The software exposure of LIMS , documentum, Trackwise will be preferable.
For all the positions, it is essential for candidates to have exposure in regulatory requirements of documentation and cGMP/GLP.
Kindly note : The role is required to do the analysis and not the review.
Interested candidates please share their resume at manan.hathi@zyduslife.com.
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Greetings from Zydus Pharmaceuticals Ltd!!!
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 manan.hathi@zyduslife.com for further evaluation.
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