c.v for bulk drugs.doc

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V.Madhav Rao Mobile: 09397110352 Email: [email protected] Objective: A desirable position in Quality Assurance and seek a close association with pharmaceutical industry utilizing my technical knowledge and expertise. Contribute significantly towards the growth of the industry and be a keen learner throughout. EDUCATIONAL QUALIFICATION M.Sc., Biochemistry from Andhra University affiliated college RITAMS Tanuku West Godavari, A.P (May2001/69%) B.Sc., Biochemistry, Biotechnology and Chemistry from Andhra University M.V.R Degree College Gajuwaka, A.P (April 1998/ 65%). Pharmaceutical Experience: Organization: Sri Vyjayanthi Labs (p) Ltd, Vishakhapatnam. Duration October 2011- to till date. Designation: Working as Executive in Quality Assurance. Key Responsibilities: Ensure internal audits are carried out as per schedule and necessary corrective and preventive actions are taken. Ensure maintenance and calibration of equipment/instrument as per schedule Update Customer Specs format, Vendor Questioner and other Quality documents. All GMP documents shall be maintained and started with good trainability.

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V.Madhav Rao Mobile: 09397110352 Email: [email protected]:A desirable position in Quality Assurance and seek a close association with pharmaceutical industry utilizing my technical knowledge and expertise. Contribute significantly towards the growth of the industry and be a keen learner throughout.

EDUCATIONAL QUALIFICATIONM.Sc., Biochemistry from Andhra University affiliated college RITAMS Tanuku West Godavari, A.P (May2001/69%)B.Sc., Biochemistry, Biotechnology and Chemistry from Andhra University M.V.R Degree College Gajuwaka, A.P (April 1998/ 65%).Pharmaceutical Experience: Organization: Sri Vyjayanthi Labs (p) Ltd, Vishakhapatnam.

Duration October 2011- to till date.

Designation: Working as Executive in Quality Assurance. Key Responsibilities: Ensure internal audits are carried out as per schedule and necessary corrective and preventive actions are taken.

Ensure maintenance and calibration of equipment/instrument as per schedule

Update Customer Specs format, Vendor Questioner and other Quality documents.

All GMP documents shall be maintained and started with good trainability.

Approving procedures like SOPs, Specs, MOAs, BPRs, Master formulae, forms etc.

Handled customer queries to meet their expectations. Analysis of customer complaints. Work with Production personnel in an advisory role to assist them with quality issues within their department. Handling of internal and external calibrations of instruments and equipments. Ensure deviations & OOS are investigated and necessary correction, corrective and preventive actions are implemented. Approve all proposed changes that potentially affect to the intermediate and API quality attributes.

QA Release of Finished Product to the market based on the customer requirements and planning. Handling of products - change controls and planned deviations and ensuring that they are closed properly.

Release of finished products (API & Intermediates) for sale after review of all the Batch Production Records, related documents and ensure compliance to GMP requirements prior to release.

Review and revise with necessary changes/periodical review of standard operating procedures in all departments.

Maintain accurate record of labels and documents related to QA release.

Review & maintain the all product specimen labels as per the requirement.

Conduct the investigations through inter department core teams on need base marketing complaints and on failure batches

Conduct the internal audits and vendor audits to maintain the Quality as per the established procedures.

Coordinate and approve the process validations and Qualification protocols and reports.

Conducting the GMP classes for the new trainee and for all the employees as per year schedule. Preparation of Audit response for the customer audit.

Preparation of Investigation report of unplanned deviations.

Preparation of ISO Documentation procedures, manuals, standards and specifications. Participate in the Environment, Health & Safety audits. To distribute the relevant documents to concerned departments.

Planning, execution and monitoring of complete stability program.

To receive, review, approve and archive all records relating to the manufacture, testing and packaging of the companys products. Handling of Training - On Job And cGMP Handling of Annual Products Review of ProductsResearch Experience Organization: NiTza Biologically (p) Ltd HYDERABAD, Andhra Pradesh. Duration Aug 2009 to April2013 Designation: Technical Head

Key Responsibilities in NiTza Biologicals (p) Ltd in: Job profile:

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.

Training the post graduate students of the life science as part of their fulfillment of master degree in different techniques of respective topics. Preparation the thesis for the students for M.phil and Ph.D Degree. Training the staff as part of on job training in the subject of Microbiology and biochemistry.

Conducted workshops in Enzymologists in and around A.P, ODISA, and CHATISGARRH AND JARKHAND.

Academics Experience: Organization: D.N.R. Degree College and P.G Center. Bhimavaram.West Godavari. A.P Duration: 2001 2009. Designation: Head of the Department Biochemistry and Biotechnology.

Key Responsibilities: Department founder and H.O.D. for Biochemistry & later 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 ofStudies in Biochemistry & Biotechnology Departments for the years 2006 to 2009 in D.N.R. College.

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.

Other Activities: Programme coordinator for Blood Grouping Camp in the College for the years 2005 & 2006 conducted by Association of Life Sciences, D.N.R. College.

Conducted National & State Level seminars in the year 2006&2007.Strengths: Highly motivated and result oriented professional with strong analytical and team building skills.

Ability to convert technical skills into practical applications.

Good exposure in management, planning and presentation skills.

Clear, articulate communicator: Excellent interpersonal, verbal, and written communication skills.

Productive and responsible team player: Embraces challenges and enjoys learning new things.

Proven ability working in fast paced deadline environments managing multiple tasks. Trained the candidates of different field in communication skills and personality development. Computer savvy: Well versed with operating system like windows2008,2003, and windows XP professional and soft ware packages like MS Office word and Excel.Address for correspondence:

Name: V.Madhava Rao

Dr.No:9-5-94

New GajuwakaVishakhapatnam -530026

Andhra Pradesh.

Email: [email protected]: 09397110352.

I here declare that the above furnished details are true and correct to the best of my knowledge and belief.

Place: Vishakhapatnam

Date: