Ajanta Pharma Walk-in Interviews for QA, QC & Production (Manufacturing OSD) on 26th Jun 2022 (Sunday)
About Company
Ajanta Pharma Limited, a specialty pharmaceutical company engaged in development, manufacture and marketing of quality finished dosages in domestic and international markets. Ajanta operates 7 state-of-the-art manufacturing facilities in India. 2 of the facilities in India have been successfully approved by US FDA. We are looking for suitable candidates for our formulation facility at PAITHAN, Dist- Aurangabad (Maharashtra).
Quality Control
Officer/Asst. Officer (QC) : B.Pharm/ M.Pharm/M.Sc.
Experience range: 02 to 05 years Over all experience in analysis of FP, IP, PV and Stablity samples. Handling of various instruments like IR, UV and HPLC. Expertise in Chromatography and Spectroscopy analysis.
Production (Manufacturing OSD)
Sr. Officer/Officer (Production): B.Pharm / M.Pharm with 03 to 06 years of experience. Candidates should have experience of granulation, compression, coating & capsules areas.
Sr. Executive (Production): B.Pharm / M.Pharm with 12 to 13 years of experience. Should have worked in capacity of Shift in-charge. Experience with E-BMR systems is preferred.
Quality Assurance
Officer: B.Pharm / M.Pharm/ M.Sc. with 02 to 03 years of experience. The candidate should have exposure in preparation of BMR/BPR. Experience with E-BMR systems is preferred.
Officer (Lab QA): B.Pharm/ M.Pharm/ M.Sc with 03 to 04 years experience. The candidate should have exposure of review of analytical reports (QC), instrument log books, compliance of procedure in lab, co ordination with DRA, ensure integrity of data.
Date, Time & Venue :
26th Jun 2022 (Sunday)
Follow up to reach at seme
Between 10.00 a.m. to 05.00 p.m.
The Fern Kesarval Hotel & Spa Verna Plateau, Kesarval Cortalim Goa 403 710
HOW TO REACH AT VENUE
Go to gle Play Store
Download QR code scannis app Scan the QR code (image shown let) Cick the link for Google Maps
Follow up to reach at seme
1) For all positions, candidates having exposure to regulatory requirements of documentation cGMP/GDP and worked in regulated plants shall be preferred.
2) Wearing of mask is compulsory at the venue. Maintain social distancing.
3) Interested candidates who are working with USFDA/MHRA approved facilities only, may attend interview along with updated CV, current CTC structure, 3 recent salary slips, documents of educational qualification and previous employments.
4) If unable to attend interview then forward updated CV at;
[email protected]/[email protected]
