Home / Job / Alivira Animal Health Ltd – Walk-In Interviews for Analytical R&D on 2nd Jan’ 2021 @ Ambernath (East)

Alivira Animal Health Ltd – Walk-In Interviews for Analytical R&D on 2nd Jan’ 2021 @ Ambernath (East)

Alivira Animal Health Ltd – Walk-In Interviews for Analytical R&D on 2nd Jan’ 2021 @ Ambernath (East)

Walk in interview – Analytical Research and Development – Analyst @ Alivira Animal Health Ltd

Walk in interview on Saturday, 2nd January 2021 between 9.30 am to 4 pm.

Venue :

Alivira Animal Health Ltd;

Plot no. A-68, MIDC, Near Panchatara Hotel,

Additional Ambernath,

Ambernath (East) 421 506

Analytical Research and Development Analyst (4 openings)

M.Sc, B.Pharm, M. Pharm with 1 to 8 years of experience in Pharmaceutical Formulation – ARD for regulated market. Good knowledge of analytical method development, validation and transfer, stability testing for different dosage form like Tablet, injectable and suspension etc. Experience of handling modern analytical instruments like HPLC, Dissolution etc and should be familiar with documentation activities like preparation of spec’s, STP, Protocol and Report etc.

Contact Person : Lalit Raut – 073044 40950

Required Documents:

Updated Resume, Latest 3 months Salary Slips, Increment letter and 1 passport size photograph

For more details please visit http://www.alivira.co/

Those who are unable to attend the Walk-in, may send their resume to [email protected][email protected] and [email protected]

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

About Pharmaceutical Guidanace

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

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