Rangaprakash Cherukuri
About
Rangaprakash Cherukuri is from Hyderabad, Telangana, India. Rangaprakash works in the following industries: "Pharmaceuticals". Rangaprakash is currently Director Of Operations at Valens Molecules (Fomerly Posh Chemicals Private Limited), located in Hyderabad, Andhra Pradesh. In Rangaprakash's previous role as a Exceutive-API Sourcing& Procurement at Mylan Laboratories Limited, Rangaprakash worked in hyderabad area, india until Mar 2014. Prior to joining Mylan Laboratories Limited, Rangaprakash was a Validation Engineer at SBP Global Coporation and held the position of Validation Engineer at NJ, USA. Prior to that, Rangaprakash was a Quality assurance specialist at Posh Chemicals Private Limited, based in Hyderabad Area, India from Jun 2010 to Feb 2011. Rangaprakash started working as Intern Trainee at Dr. Reddy's Laboratories in Hyderabad Area, India in May 2009. From May 2008 to Jul 2008, Rangaprakash was QA trainee (Internship) at Posh Chemicals Private Limited, based in Hyderabad Area, India.
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Rangaprakash Cherukuri's current jobs
Rangaprakash Cherukuri's past jobs
Invovled in Vendor development operations, sourcing key starting materials& general materials for API's
Wokred on a Validation Remediation Project for a Medical device company which was under a consent decree. Invovled in th Authoring, Reveiwing and Executing various validation documents like Risk assesment,validation Plan, Qualification protocols(IQ,OQ,PQ), commisioning and decommisioning reports for both Equipment and various softwares
Duties included Preparation, Issuance and Review of BPCR’s. Review COA and test reports. Preparations of SOP’s and raise change controls for the revised SOP’s and assess its impact on the process and the product. Preparation of Annual production quality records (APQR). Assessing vendor questionnaire to Qualify\Disqualify the Vendors and updating the database by coordinating with central purchase dept. Conducting Internal audit and preparing CAPA reports. Posh Chemicals is an USFDA approved facility therefore had opportunity to gain Good knowledge on cGMP requirements. Assisted in preparation of DMF of an API. Successfully faced Regulatory audits viz., USFDA and Mexico ministry of health. Also attended few Quality system and customer audits.
Trained about the unit operation in production of Active pharmaceutical Ingredients (API’s)
Trained in quality assurance department for records keeping, preparation of sops and general functioning of QA department.