Covalent Laboratories Private Limited, an ISO 9001:2008 & ISO 14001(2004) accreditated pharmaceutical company and WHO GMP certified for all its products, is specialized in the manufacturing of Cephalosporins.It has a wide range of products and is fast expanding to meet the present and future market demands for the high value, low volume drugs. Covalent Laboratories manufactures the Active Pharmaceutical Ingredient (API) in bulk quantities for both domestic and international markets.
- Qualification: MS/M.Sc(Science) in Organic Chemistry
- Experience : 00-05+years
- Role: Trainee RA
- Department:API Drug Regulatory Affairs
- Job Location: Sangareddy
Time and Venue
30 May – 7th June , 9.30 AM – 5.30 PM
Factory : Survey NO. 374, Gundla Machnoor Village , Hathnoor Mandal , Sangareddy Dist., Telangana India.phn : 9100167917
Contact – Mr. Yashoda Krishna ( 9100167917 )
Job description
The Trainee RA (Regulatory Affairs) Department will be responsible for assisting with regulatory procedures, compiling and submitting regulatory documents, and maintaining and tracking regulatory submissions and supporting to Manager & Team .
Required Candidate profile
Master’s degree ( MSc Organic Chemistry ONLY) Good communication, organizational, and analytical skills Good attention to detail and ability to manage multiple tasks effectively Good computer skills .
