Walk in Interview for M.Pharm, MSc, B.Pharm in Production at Aizant Drugs Research Solutions Pvt. Ltd
Aizant is an integrated drug development solutions provider. Aizant was established by experienced pharmaceutical professionals with global exposure. We are a rapidly growing formulation CDMO and CRO with a diverse portfolio of capabilities partnering with health care companies specializing in new molecular entities (NME’s), generics (ANDA’s) and over the counter (OTC’s) products globally.
Post : Executives / Operators
Qualifications : B.Pharmacy / M.Pharmacy / BSc / MSc / ITI / Diploma / B.Tech (Mechankal / Chemical)
Experience : Candidates with 0 to 4 years experience with good experience in Production Department as Capsule filling / Coating / Compression & Granulation operators as well as executive level with Pharmacy Background.
• For all positions, candidates having exposure to regulatory requirements of documentations CMP / GDP and worked in regulated plants shall be preferred
• Interested Candidates may Walk-In for an Interview along with their updated CV, passport size photo, Last 3 months payslips of the present employer. Latest or Previous Increment Letter. Bank statements of 6 months
• Candidates those are unable to attend Walk-In may email their updated resumes on following email ID’s for further consideration, if needed.
DATE & TIME :
Jan 7th & Jan 8th ; 3:00 PM to 4:30 PM Gate Closes at 4:30 PM
Jan 11th & Jan 12th ; 3:00 PM to 4:00 PM Gate Closes at 4:00 PM
Aizant Drugs Research Solutions Pvt. Ltd.
Sy No. 172 173 – Apparel Park Road. Dulapally, Village Quthbullapur Mandal, Hyderabad, Telangana. India
E-mail ID : [email protected]
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube