Walk in interview in Production, Packing, Quality Control at Ajanta Pharma Limited
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 and Mauritius. 2 of die facilities in India have been successfully approved by USFDA. We are looking for competent young professionals to be an integral part of our team for Formulations site at Paitlian, near Aurangabad (Maharashtra).
Production / Packing (Manufacturing OSD)
Sr. Officer/Officer (Production) : B.Pharm/M.Pharm with 02 to 06 years of experience of Production actvities such as; granulation, compression, coating & capsules areas. Packing activities such as; bottle packing, blister packing, pouch packing, track & trace system etc.
Quality Assurance (QA)
Officer (IPQA) : B.Pharm/MPharm with 03 to 05 years of experience of in-process testing of manufacturing and packing operations, line clearance, sampling, review batch records, manual, electronic data. Checking compliance as per SOP. Entering batch process data.
Officer (LAB QA) : B.Pharm/MSc with 03 to 05 years of experience of review analytical reports, instrument log book, online check of cGMP and QC analytical documents. Verify compliance as per SOP in lab. Co-ordinate with validadon and DRA team. Ensure integrity of data either manually or electronically.
Officer (QMS) : B.Pharm/M.Sc with 03 to 05 years of experience review and closure of change controls, deviations incidents, CAPAs pertaining to production dept.
Quality Control (QC)
Executive/Sr. Officer/Officer : B.Pharm/M.Pharm/M.Sc./B.Sc. with 02 to 09 years of experience of FP, in-process, process validation and stability. Handling of instruments like HPLC, GC, UV-Spectrophotometer, Particle Size Analyser. KF-Autotitrator (Metrohm), Dissolution test apparatus, QMS & LIMS, Handling of OOS, OOT incident investigation. Expertise in software qualifications and designing and validation of report templates.
Interview Date, Time & Venue
19th January 2020 (Sunday)
Between 09.00 a.m to 05.00 p.m
Hotel Woodlands NH-8, Near Desai Automobiles Balitlia,
1) For all positions candidates having exposure to regulatory requirements of documentation cGMP/GDP and worked m regulated plants shall be preferred
2) Interested candidates may "Walk-in" for an interview alongwith their udpated CV, Passport size photo, latest annual] CTC breakup and relevant documents.
3) Candidates working in USFDA & MHRA approved facilities only , those are unable to attend walk-in may email then updated resumes on following email IP's for further consideration, if needed
email@example.com / firstname.lastname@example.org
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