V.Madhava Rao

Mobile: +91-939*******

Mail: ac2lwe@r.postjobfree.com

Pharmaceutical Experience

Organization: Sri Vyjayanthi Labs Pvt. Ltd. Andhra Pradesh.

Duration: 13th June 2011 to till date.

Present designation is Manager-QA

Reviewing completed production batch record and laboratory records before releasing API’s Intermediates for distribution.

Planning the internal audits.

Preparing/Reviewing the validation protocols and reports.

Preparing / Reviewing the APQR.

Preparing and reviewing the SOP.

Checking and approving the BPCRs after completion.

Review and approval of qualification protocols and reports for instruments and equipments.

Calibration records review.

Executed various validations like analytical method,cleaning,drying Blending and process validations

Checking the records for the proper maintenance of environment, safety and health of the working personnel.

Making sure that effective systems are used for maintaining and calibrating critical equipments.

Making sure that the materials are appropriately tested and the results are reported.

Making sure that there is stability data update to support retest or expiry dates and storage conditions on API or Intermediates.

Inspection of production operation periodically and check on the implementation of Standard Operating Procedures (SOP) during the Production operation.

Checking the house keeping and cleanliness of the work places.

Evaluating the clean room procedures and cleanliness of the working personnel in all departments.

Maintenance of job, service, skills, training records of all personnel working in the technical and Pharma areas.

Giving CGMP training to the all department personnel.

Preparing/reviewing the internal audit schedules and checklists.

Vendor and Supplier Qualification.

Logging and handling the investigations for deviations, OOS and providing CAPA for the same.

Co-ordinate with Production, QC, warehouse and Maintenance regarding non conformance & corrective action for the same.

Provide support to the various divisions for effective and efficient implementation of the Quality Management System.

Worked as core internal auditor in the facility.

Customer audits faced and CAPA submitted-06

Customer audits co-ordinated-53

Compiled and submitted CMC Documents for SVLL customers.

Faced Drug control, ISO-22000 and ISO 9001-2008 audits.

Member of safety committee in this site since 2013 to till date

Research Experience

Organization: NiTza Biologically (p) Ltd HYDERABAD, Andhra Pradesh.

Duration August 2009 to May 2011.

Designation: Sr. Scientific officer.

Key Responsibilities in NiTza Biologicals (p) Ltd:

Served as a technical resource person.

Ensure the laboratories operations adhere to the elements of good lab practice, such as Lab documentation, methods of analysis i.e.STP’s SOP’s, verifiable training of analysts, and applicable standards of quality control and quality assurance.

Ensure reliable and efficient laboratory operations, calibrations were done as per schedule.

Manage those individuals responsible for lab operation, implement and manage test schedules.

Maintenance of lab schedule, cGLP compliance.

Training analysts on lab methods.

Prepared technical documents such as reports, operating procedures, methods, and study protocols.

Designing the work plan for the new research projects and preparing cost analysis of the research works.

Responsible for advanced discovery research and developing new technology in the areas of interest to NiTza Biologicals.

Guided the post graduate students of the life science as part of their fulfillment of master degree in different techniques of respective topics of different regions students in India and helped them in preparing the thesis of not less than 150 students.

Training the staff as part of on job training on the techniques of Microbiology and biochemistry.

Conducted workshop’s in Enzymology in and around A.P, MAHARASTRA, ODISA, and CHATISGARRH AND JARKHAND not less than 50 workshops.

Academics Experience:

Organization: D.N.R. Degree College and P.G Center. Bhimavaram.

West Godavari. A.P Duration: June 2002 –July 2009.

Designation: Head of the Department Biochemistry and Biotechnology.

Department founder and H.O.D. for Biochemistry & later worked as in charge for Biotechnology Departments in D.N.R College since 2001 to 2009 in D.N.R. (Autonomous) Degree College, Bhimavaram. A.P.

Chairperson for Board of Studies in Biochemistry & Biotechnology Departments for the years 2006 to 2009 in D.N.R. College.

Worked as practical examiner for autonomous colleges from 2003-2009.

Worked as Deputy Chief Superintend for Intermediate exams from 2008-2009.

Worked as core committee member for NAAC accreditation in the year 2005.

Worked as Life science coordinator for the years 2005, 06, 07, 08 & 09.

Worked Admission committee Secretary from 2007-2009.

Served as staff Secretary 2007-2009

Organization: Ritam’s Degree College and P.G Center. Tanuku

West Godavari. A.P Duration: May 2001 –May 2002.

Designation: Lecturer in Department of Biotechnology

Worked as Lecturer for both Post graduation and Degree Biochemistry.

Worked as internal examiner for the P.G and Degree Practical examinations.

EDUCATIONAL QUALIFICATION

M.Sc., Biochemistry from Andhra University affiliated college RITAMS Tanuku West Godavari, A.P (May2001/69%)

Strengths

Very flexible and adaptable to change.

Responsible, operate with integrity and team work.

Learning attitude and logical approach.

Computer literacy skills in programs that applicable to role, solid written and Verbal Communication skills.

Technical Skills

Computing skills

OS XP, Vista & Windows 7

Packages MS Office 2003 and MS Office 2007

Personal Details

Date of Birth: 14.08.1975

Address: V.Madhava Rao

S % V.Venkateswara Rao

Dr.No. 95-5-94, Jogavani Palem

Gajuwaka, Visakhapatnam,

Andhra Pradesh - 530026

Languages’ known: Telugu, English& Hindi.

Date: 14.08.2017

Contact this candidate