Walk in Interview for R&D Department @ Maithri Drugs Private Limited on 2nd jan’2020| 15 posts
MSN Group is one of the fastest growing manufacturers of Active Pharmaceutical Ingredients (APIs) and Finished dosages in India. Established in the year 2003, MSN Group comprises of 330 API manufacturing plants (including one for Oncology), three finished dosage facility ( including one for Oncology)and a dedicated R&D Center . Our plants are ISO 9001-2000 certified, WHO: GMP, EU:GMP and USFDA approved. Our manufacturing units are designed to confirm to the principles of Quality, Safety and sound Environment.
API Division : R&D Department
Trainee’s/ Junior Executive’s/ Executive’s/ Senior Executive’s
Eligibility Criteria : B.Sc (Chemistry)/M.Sc (Organic Chemistry) with minimum 0-6 yrs of work experience.
No of Posts : 15
1. Need to have sound knowledge in API R&D.
2. Need to have experience in process developmemt R&D
3. Should be able to handle SCM activities related to R&D
Documents to be carried : Candidates are requested to carry Recent passport size photograph (MUST), Updated resume, Photostat copies of Educational Certificates, Latest Increment Letter, Last 3 Months Pay Slips, Last 6 Months Bank Statement and Photostat copy of Aadhar Card…
Venue & Job Location : Maithri Drugs R&D Technology Center, Gummadidala.
Landmark : 2nd gate beside IPC Church, Gummadidala
Note : Free transport is provided for selected candidates from Balanagar X Roads and Kukatpally and also subsidiary canteen food is provided.
Only MEN Candidates may walk-in from 09:00 AM to 12:30 PM
Interview on 02nd January 2021, Saturday
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