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Walk in Interview on 3rd october 2020 for M.Pharm, B.Pharm @Sri Krishna Pharmaceuticals Ltd

Walk in Interview on 3rd october 2020 for M.Pharm, B.Pharm @Sri Krishna Pharmaceuticals Ltd

 

Sri Krishna Pharmaceuticals Ltd (SKPL), established in 1974, started life as a pioneer in the bulk manufacture of acetaminophen (Paracetamol) for the domestic Indian market. Today, the company is a vertically integrated bulk manufacturer of multiple first-line-of-defence APIs, PFIs and finished dosage drugs. Paracetamol is still very important to the company and the company remains one of the largest manufacturers in the world.

Formulation R&D
Qualification: B. Pharma/M. Pharma
Experience : 3 yrs. to 4 yrs.
Exposure : Develop products or dosage forms for Nutraceutical, experience of microencapsulation and vitamin stabilization project, Feasibility study of diversifying product range such as carotenoids, Plant extract, food fortification etc
B. Pharma or M. Pharma fresher’s can also walk-in for Trainee Level

Formulation Analytical R&D
Qualification: B. Pharma/M. Pharma, MSc
Experience : 3 yrs. to 6 yrs.
Exposure : Must have experience in Method Development, any one from API or OSD can attend but should have Method Development experience.

If you are interested and having similar background then attend F2F interview on 3rd Oct 2020 at 11:00 AM.

Interview Venue Details
Sri Krishna Pharmaceuticals Limited
Unit-IV: Survey No 296/7/10, IDA, Bollaram, Jinnaram Mandal 502 325
Medak District, Telangana, India

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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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