Aizant Pharm- Interview For Quality Control Manufacturing Formulation on 8 June, 2024

Aizant Pharm- Interview For Quality Control Manufacturing Formulation on 8 June, 2024

Aizant Pharm- Interview

Aizant Pharm Walk In Interview For Quality Control Manufacturing Formulation
Quality Control – Manufacturing Unit – Formulations
Department : Eligibility
Stability : 4-6 yrs of exp in Disssolution, HPLC, Stability Sample Management, RS
Raw Materials : 2-3 yrs of exp in Sampling of Raw Materials & Packing Material, Raw Materials(Core)
Analytical Method Validations : 3-5 yrs of exp in Core Experience in Analytical Method Validations, Handling of HPLC, Dissolution instruments

Microbiology : 2-3 yrs of exp in aware of environmental monitoring, Culture media prepartion, MLT Testing
Date: Saturday, 08 June, 2024
Time: 09:00 AM
Venue: Aizant Drug Research Solutions Pvt. Ltd.
Sy. No. 172 & 173. Apparel Park Rd. Dulapally, Quthbullapur Mandal, Hyderabad. Telangana 500100
Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

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Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 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

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