Walk In Interview 30th Aug to 7th Sept 2022 At Covalent Laboratories

Walk In Interview 30th Aug to 7th Sept 2022 At Covalent Laboratories. 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. 

Covalent Laboratories Pvt Ltd invites Experienced, Dynamic & Self-Motivated Professionals  for the below positions at the Hyderabad/Secunderabad location. 

Covalent Laboratories Pvt Ltd  is recruiting for the accompanying positions:

-Production

-Quality Control 

 -R & D

-Regulatory Affairs

Refer Notification & all relevant information below. Interested and qualified applicants can attend at scheduled time.

Opportunity subtleties:

Department:Production/ R & D/Quality Control/Regulatory Affairs

Post Name:Chemist / Sr. Chemist / Jr. Executive/ Executive - Production/ R & D/Quality Control/Regulatory Affairs

Capability: Any Graduate/B.sc/M.sc

Experienced:3 to 8 years

Set of working responsibilities: Covalent Laboratories Pvt Ltd  Hiring For Chemist / Sr. Chemist / Jr. Executive/ Executive - Production/ R & D/Quality Control/Regulatory Affairs !

Significant Details :

Place: Hyderabad/Secunderabad

Walk in Interview Date: 30th Aug to 7th Sept 2022

Time:9.30 AM - 4.00 PM

Walk In Address:-Covalent Laboratories Private Ltd.s (P) Ltd.Gundla Machanoor(Village), Hathnoor (Mandal), Sangareddy (Dist), Telangana, INDIA-502 296

Contact : Mr. Shiva ( 9100167917 )

Choice Process: The determination will be based on Interview.

Set of working responsibilities:

Chemist / Sr. Chemist / Jr. Executive/ Executive - Production

Monitoring of production process, inprocess checks and changeover

GMP incidents.

Investigating deviations, OOS and violation of GMP incidents.

BMR/BPCR change control forms CCF.

Training on SOPs to subordinates.

API CRO, HPLC / LCMS & Method development / Regular analysis

Responsible for testing of all In process, Raw material, Intermediate, stability samples , cleaning samples and Finished products analysis of HPLC/UPLC/GC as per Standard testing procedure.

Preparation of LOA (Read and understanding the requirement).

Hands on experience on Drafting of response to the DMF related queries and Technical queries. Preparation of Applicant part and Restricted part DMFs (USDMF and EUDMF).