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Walk in interview in Quality Control, R&D & ARD at Covalent Laboratories

 

Clinical courses

 

Clinical courses

Covalent Laboratories Private Limited is an ISO 9001:2008 & ISO 14001(2004) accreditated pharmaceutical company and WHO GMP certified for all its products Covalent Laboratories is specialized in the manufacturing of Cephalosporins and its intermediates. It has a wide range of products and is fast expanding to meet the present and future market demands for the high value drugs. It manufactures the Active Pharmaceutical Ingredient (API) in bulk quantities for both Indian and international regulated and semi-regulated markets. All the drugs manufactured meets USP / BP / JP standards.

Chemist/Sr.Chemist/Jr.Chemist(R&D & ARD)
M.SC (Organic Chemistry with 1-3 Years hands on experience in R&D Department and for AR&D with B Sc / M. SC Analytical Chemistry) having 1-3 Years experience in handling of HPLC, GC, UPLC Preferences will be given to candidates having experiences on handling of LCMS In relevant Bulk Drug Manufacturing Companies of repute.

Chemist/Sr.Chemist/Jr.executive(Quality Control)
B.Sc, M.Sc with 2 to 8 years experience in handling of HPLC, GC with head space. UV. IR.Polarimeter instruments, in addition to routine chemical analysis. Experience In, empower/ relevant software is desirable. Should have sound knowledge of GMP and related documentation practices and Knowledge of OOS / OOT and handling of laboratory incidents / stability studies and its documentation.

 

Chemist/Sr.Chemist
B.SC with 1 to 3  years hands on experience in Powder Processing /Packing Area in any Bulk Drug Companies.

Intersted candidates may email their resumes : bpvreddy@covalentlab.com

COVALENT LABORATORIES PVT. LTD.,
Attn. HR-Factory H.O: # 8-3-677/18,2nd floor, S.K.D. Nagar,
Yallareddyguda, Hyderabad -500 073

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