Resume CV : Analytical Chemistry, Quality Control and Management

[ravindrakhot]

Date : 20.04.2010
Dear Sir,

Few important things about me :
I can be best described as ever happy, positive and having a vision for self as well as for the family. I have my own set of objectives in my personal life and always strive to achieve them. The values taught by the parents and the experiences gained so far makes me believe that success/ money shall not be chased. It will automatically come if I work sincerely and give my best. I believe in myself. Respect the values and know the cultural and business ethics. I am strongly influenced with the human psychology and read a lot about it. I like to admit that like everyone else in this world I have made mistakes and have learned a lot from them. I have rich experience of industries for the last 17 years and all throughout my experience with the industries and society, I believe that Honesty, simplicity and working through the minds of people can only pave rich dividends.

My Quest : To challenge own self with new challenges in life
My Belief : Challenges met with confidence are sure shots towards success

The assignments handled as of date include :
- Lead Auditor for ISO 9001 :2008 / ISO 14001:2004 / BS OHSAS 18001:2007 and Integrated Management System Auditor
- Industrial Chemicals Manufacturing with Quality assurance
- Statutory compliance as per Integrated management system
- Budgeting /cost controlling/ Monitoring
- Planning, procurement and inventory management
- Cost reduction/ energy conservation/ process improvement program initiatives
- Management Representative for ISO 9001 :2000 and Environment coordinator for ISO-14001 and Implementation of both the systems
- FIVE S, TPM activities.

This has given me valuable hands on experience, knowledge, exposure and Confidence in these areas to thoroughly understand functions and run the operation. I am sure my experience, knowledge, sincerity and determination to serve the company with honesty, sincerity and positive attitude will contribute in the organization's growth and prosperity.

Thanking you.
R.N.KHOT My Resume is on next page

RESUME :
RAVINDRA.N.KHOT
Email : ravindrakhot AT rediffmail.com

The existing responsibility :
As Lead Auditor April 2006 –
· Auditing various organizations [industries/institutes] for conformance to ISO 9001, ISO 14001 & BS OHSAS 18001 requirements, Integrated Management System, market development, etc.
· Bureau Veritas provides system certification services viz. QMS [ISO 9001 :2008], EMS [ISO 14001:2004], BS OHSAS 18001:2007, etc.

Brief :
Founded in 1828, Bureau Veritas is an international group specialized in the inspection, analysis, audit, and certification of products, infrastructure (buildings, industrial sites, equipment, ships, etc.) and management systems (ISO standards etc.) in relation to regulatory or voluntary frameworks.
Bureau Veritas ranks as the world's second largest group in conformity assessment and certification services in the fields of quality, health and safety, environment, and social responsibility ("QHSE") and the world leader in QHSE services not including commodity testing. Bureau Veritas is recognized and accredited by major national and international organizations.
Bureau Veritas is present in 140 countries through a network of 850 offices and laboratories. At the end of 2007, it has more than 33,000 employees and a client base of more than 300,000.

Education :
1 I did my Bachelor Degree in Science from The New College, Kolhapur in the year1985 and Master Degree in Analytical Chemistry from Institute of Science, Mumbai in the year1987.
2 Sun Java programming with JDK 1.2 using UML std. - 25.4.2001, NIIT – Mahad

Details of work experience :
Bureau Veritas Certification India P. Ltd.
1 Working since April 2006 as Lead Auditor for ISO 9001 :2008, ISO 14001:2004 & BS OHSAS 18001:2007 standards and Integrated Management System.
2 Preparation of audit plan and forwarding it the customer
3 Ensuring travel & if required staying arrangement for the audit team
4 Conducting opening meeting
5 Leading a team of auditors for the actual audit
6 Interaction with top management of the customer for briefing the audit findings
7 Conducting closing meeting
8 Audit findings/preparation and sending it to the customer
9 Closure of nonconformities, forwarding audit report for approval
10 Ensure issuing certificate to the customer, collecting customer satisfaction feedback & forwarding it the back office
11 Support to the back office for business development, etc.
12 Awareness trainings on QMS.

Akzo Nobel Chemicals India Ltd. - Mahad :
1 Worked since December 1996 to 2006
2 The company is based in Netherlands.
The company is operations in 4 main areas :
Coating/pharmaceuticals/ chemicals/surface chemistry.

Kesar Petroproducts Ltd., Lote Parshram :
1 Worked since January 1993 to June 1996
2 Manufacturing Bisphenol-A, worked as ‘Senior Chemist’.

ITA Lab Private Limited, Mumbai :
1 Worked since November 1987-January 1993
2 Government approved / Third party inspection laboratory, worked as ‘Analytical Chemist’.

The career at Akzo Nobel Chemicals India Pvt. Ltd :
1 Joined as Assistant Manager Quality Control and Management Representative for ISO 9001 :2000 in 1996
2 Was trained at Research center in The Netherlands for basic knowledge in Organic peroxides in 1998
3 2000 : Was promoted as Manager Quality Control.
4 2001 : Direct reporting to Site In charge
5 2004 : Shouldered additional responsibility as Manager Purchase
This working in Managerial position and a member of Management Committee that involves strategically planning for business operation including factory operation.
1) Prepare SOPs based on latest developments in the testing methods as per the international guidelines.
2) Prepare and plan periodic internal QMS audit and its reporting the Management review meeting.
3) Identify training needs and execution of the same.
4) Total Productive maintenance system/workers training/ check list.
5) Analysis of break down/ Preventive and predictive maintenance System implantation to keep the down time to minimum.

QHSE, ISO 9001, ISO14001, 18001 :
1) System Implementation monitoring of ISO 9001, ISO 14001 and BS OHSAS 18001 for the last 6 years.
2) In charge of Quality Control, QMS, Purchase. Adhering to international standards.
3) Preparing the Quality POLICY, Quality Manual, Departmental procedures, SOPs for ISO 9001, ISO 14001, BS OHSAS 18001, in the direction of Group policy, International standard Implementation of these policies, Preparation and tracking of Management Program, Audit plan, Review of NCs,
4) Designing of components and KPI, Targets, Improvement Plan, its analysis etc., for Bench marking, as per the requirement of International Standard and local statutory requirement like Pollution control Board, Factory Inspectors, etc.
5) 5S implementation and Monitoring
6) Implementation of Preventative maintenance (TPM) for all plant and work as a pillar for the service group. Dealing with the essential services for customer, plant employees and contractors. Working for improving the services at al levels of the company.
7) Conducting Internal audit & Management review meetings with department wise and with Management for implementation of ISO 9001 systems.
8) Liaise with external agencies viz. certification bodies.

ACEDEMIC QUALIFICATION :(and other Training/Course attended)
1 Master Degree in Analytical Chemistry from Institute of Science, Mumbai in the year1987.
2 Diploma in Computer Application [Java] from NIIT.
3 Leadership qualities training at MRA Panchagani
4 IRCA approved QMS 9001 :2008 Lead Auditor Transition course [up-gradation], conducted by Bureau Veritas dt. 09th December 2008 at Pune.
5 IRCA approved OHSAS 18001 :2007 Lead Auditor course [up-gradation], Lead Auditor course conducted by Bureau Veritas dt. 24th Aug 2007 at Indore.
6 IRCA approved OHSAS 18001 :1999 Lead Auditor course, conducted by Bureau Veritas dt. 3rd to 5th April 2007 at Indore.
7 IRCA approved ISO 14001 :2004 Lead Auditor course, conducted by BVQI dt. 10th to 14th July 2006 at Nasik.
8 Analytical and Safety Training undergone at research center in Akzo Nobel Chemicals, The Netherlands for about 18 days
9 Have gained inspiration through Shiv Khera program – Blue Chip for Success
10 Have improved own working style through trainings taken on Total Productive Maintenance. 11 Implementation of Preventative maintenance (TPM) for all plant and work as a pillar.
12 Well coordinated Five S activity throughout the organization
13 Added up knowledge in business through practical training on Operating working capital, 14 Supply Chain Management (SCM), Customer Relations Management (CRM), Business Principles and many more.

Achievements, which have won accolades :
F Appointed as Management Representative [lead auditor] for ISO 9001 :2000 (QMS) in the organization
F Instrumental in winning 3rd position in Pune region for Akzo Nobel Chemicals (India) Limited towards effective implementation of QMS systems in the organization. This award was given by Total Quality Forum, Pune.
F Constructively reduced paperwork in the organization through right implementation of software for ISO documents making communication & systems accessible & reachable to all employees

[Guest]

Latha.K.N.
Email ID :latha.d2814 AT yahoo.in

OBJECTIVE :
To obtain a potential a long-term position where my knowledge, skills and experience are Apply utilized and challenged to meet the needs of growing global-minded company.

INNOVATIVE :
Consistently analyze and improve capabilities related to the field there by increasing the efficiency and completion with fast growing technologies.

ACADEMIC QUALIFICATION :
1. Graduation : Bsc – Chemistry, Botany, Zoology from Maharani Lakshmi Ammanni College. Bangalore.
2. Post Graduation : Msc-Biotechnology from Bangalore University (East West College).

PROFESSIONAL EXPERIENCE : 3 years

AREA OF INTEREST :
To work in Quality control/ Quality Assurance.

EXPERTISE IN :
- Preparation of SOPs, Documentation, Internal Audits.
- Good Exposure on regulatory guidelines from USP, IP, BP.
- Good knowledge of cGMP & GLP.
- Investigation of Quality Alerts, Quality incidents.
- To track for the completion and implementation of Action Plans.
- Good exposure in maintaining Microbiology Culture.
- Identification of microbiological contaminants in water, food and pharmaceutical excipients.

SUMMARY :
1. Organization : Ce Chem. pharmaceutical pvt ltd. Peenya industrial area. Bangalore.
Duration : From Jan 2007 to May 2009.
Designation : Quality control and Quality Assurance Chemist.

2. Organization : Mahendra labs pvt ltd, peenya industrial area. Bangalore.
Duration : From Oct 2009 to till date.
Designation : Quality control and Quality Assurance.

WORK EXPERIENCE IN QUALITY CONTROL :
- To carry out the process as per GLP.
- Preparation of SOPs & working procedures.
- Calibration of instruments & Documentation.
- Sampling of raw materials, packing materials, finished products & its record.
- Complete analysis & records of all raw material including graphs, Charts etc.
- In process Quality control and its specification.
- Sampling of intermediate bulk & its analysis to meet the specification.
- Sampling of finished product and release for distribution and its record.
- Analysis of all finished product & its record including graph, charts etc.
- OOS investigation – complete data investigation & its documentation.
- Method validation & its documentation.
- Maintaining of Reference Standard &Working Standard.
- Maintaining & periodic review of control samples & its documentation.
- Stability study & its written program.
- Internal and External Auditing was done successfully.

Instrument handling :
1. PH Meter.
2. Dissolution apparatus.
3. Disintegration time.
4. Friability apparatus.
5. Karl Fischer Titrator.
6. Leak test apparatus.
7. U.V spectrophotometer.
8. Polari meter.
9. Photo fluorimeter.
10. Refractive index.
11. Potentiometer.
12. TLC
13. HPLC

WORK EXPERIENCE IN MICROBIOLOGY LAB :
- Maintenance of cultures subculture and its records.
- Preparation & sterilization of culture media required for all the microbiological test
- Identification of microorganisms by different type of staining methods.
- Sterility test of sterile bulk raw materials, dry powder, packing materials (rubber stopper).
- Performed environmental monitoring of production area and microbiology lab by settle plate method & air sampler.
- Performed microbial test for water, raw materials, Empty hard gelatin capsules & excipients.
- Performed lactic acid Bacillus spores count.
- Performed swab testing to avoid cross contamination.

WORK EXPERIENCE IN QUALITY ASSURANCE :
- Implementing the GMP & quality systems and training awareness to my organization.
- Monitoring the facilities & Equipment.
- Knowledge of HVAC system & to protect against cross contamination.
- Documentation : MVP, Site master file, Sops, Work instructions, and MFR.
- Validation and its Documentation.
- BMR &BPR preparation accordingly to laid down procedure.
- Review & approval of batch records before release of products.
- Carry out the in process checks as per the quality norms.
- Monitoring the manufacturing and packing activities.
- Line clearance for all respective activities and its records.
- Monitoring the Raw/packing/Finished product storage condition.
- Verifying the QC raw data for finished goods release to exist market.
- Handling change control, Deviation and its Documentation.
- Vendor Approval & its documentation.
- Training program and its Records.
- Define, Develop and demonstrate job competence.
- Conduct planned and its periodic audits.
- Self-inspection & Quality Audit Records.
- Internal & External Audit is done successfully.

SOFTWARE SKILLS :
Basic Knowledge : MS DOS, WINDOWS, EXCEL.

STRENGTHS :
- Believe in my self-confidence.
- Full commitment to my work.
- Problem- solving skills, Good communication & management skill.
- Willing to learn new things and technologies to get job done.
- Work independently & as a part of team.

[Guest]

I want CV for R&D QC Qa i am Fresher