This curriculum vitae summarizes the professional experience and qualifications of Dharmendar B.S. He has over 9 years of experience working in quality control at Biocon Limited, a leading biopharmaceutical company in India. He holds an MSc in Biotechnology and BSc in Chemistry, Botany, and Biotechnology. His role at Biocon involves ensuring quality standards, analyzing samples, maintaining laboratory instruments, developing methods, handling audits, and more. He has knowledge of cGMP, analytical instruments, and seeks to continue learning and growing in his career.

1. CURRICULUM VITAE
Dharmendar B.S.
# 58,4th cross, Widia layout,
Chandra layout, Vijayanagar,
Bangalore 560040.
Mobile No: 9886998501
Email ID: dharmebs29@yahoo.com
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OBJECTIV:
To work in tandem with a team in a challenging and competitive environment where I could improve my knowledge,
capabilities and put them to use for the development of the organization.
Name : Mr. Dharmendar B. S
Date of birth : 28th
April, 1983
Languages known : English, Hindi, Kannada.
(To read, write and speak)
Father’s name : Late Sadashiaviah. B
Nationality : Indian
Hobbies : Reading, Music, Sports etc
STRENGTH:
1. Scientific knowledge and understanding (analytical chemistry)
2. Thorough understanding of cGMP, ICH guidelines.
3. Scientific interpretation of regulations and scientific advice.
4. Experience in working with major biotech like BIOCON
5. Presentation skills.
6. Communication skills in English.
7. Meeting deadlines.
8. Analytical skills and problem solving
9. Understanding of finance and economics.
EDUCATION QUALIFICATION:
MSc Biotechnology, PESIT College Bangalore.
BSc Chemistry, Botany, Biotechnology. Government science college Bangalore.
Currently working as Deputy Manager at ‘’Biocon Limited’’, A leading Biopharmaceutical company, referred to as the
Biotech major, the largest Biotech company of India since June 2007.
PERSONAL INFORMATION:
PROFESSIONAL INFORMATION:

2. CURRENT JOB PROFILE:
Overall 9+ years of working experience, I offer includes
 Planning of work within the team.
 Raw material, In-process, finished product inspection/testing/approval.
 Product traceability.
 Customer complaints relating to quality of the product.
 Identification recording and evaluation of all Nonconforming products.
 Corrective and preventive actions as and where applicable.
 Adherence to GLP.
 Maintenance and calibration of all instruments.
 Preparation/review and maintenance of quality records.
 Training of personnel in QC.
 Preparation/review of product specification and analytical reports.
 Review of cleaning validation/process validation protocols.
 Preparation and review of analytical method validation protocols and method transfer records and reports.
 Updating stability protocols and calibration records.
 Investigation of OOS.
 Handling of product recall.
 Review of change controls.
 Handling of customer complaints.
 Customer audits and follow ups.
 Responding and complying to audit observation.
 SAP
 Vendor qualification, making key RMs trend as per vendors. Updating of OOT to superiors.
 New method development and validation for raw materials.(Developed GC purity method to analyze 21 different
solvent in single method)
 Investigate deviations, incidents in lab, out of specifications under GMP and ISO guidelines.
 Co-ordination with R&D for technology transfer,method transfer.
 Maintaining Primary and analytical standards. Preparation of analytical working standards, solutions and
maintenance of impurities.
 Testing of fermentation and synthetic product intermediates at in process stage. Developed kjeldhal method of
analysis by Skalar instrument to analyses nitrogen & phosphate in fermentation raw material & in in-process
samples.
 Prepared short Observation raw data which reduced writing work.
 Submitting analytical reports to Regulatory authority & handling regulatory quires.

3. EXTRA SKILL:
Multi-task oriented, versatile and adaptable.
Aggressive and highly motivated, quick learning capability.
Excellent knowledge of CGMP, vendor qualification & Regularity Affairs.
Knowledge of MSDS,GMP, GLP,USP,BP,and SOP. Experience in operating analytical Instruments.
(HPLC,GC,FTIR,SKALAR, RAMAN,TLC,UV Spectrophotometer etc.)
INSTRUMENTS KNOWLEDGE:
 High pressure liquid chromatography (Agilent software)
 Gas chromatography (Agilent software)
 FTIR (Thermo nicolet)
 particle size analyzer (Malvern mastersizer 2000)
 UV spectrophotometer (Shimadzu)
 Melting point apparatus (Buchi M-565)
 Karl-fischer/Auto titrator (Metrom)
 Polarimeter (Rudolph auto pol V)
 Viscometer (Make : Anton paar)
 SKALAR
 Homogenizer (IKA)
 Centrifuge (Remi)
 Refractometer (Make :Anton paar)
 Raman instrument (BW tech)
 Densitometer (Make : Anton paar)
 Analytical balances
 pH and conductivity meters
AUDIT EXPERIENCE:
 Been a successful auditee for audits conducted by various national and international pharmaceutical regulatory
organizations such as WHO, usfda, euGMP, MHRA, MOH, etc.
 Been a successful auditee for audits conducted by various national and international customers.
 Been a successful auditee for audits conducted by various national and international management system
implementation organizations such as ISO9000 and ISO14000.
 Been a team member in the implementation of KAIZEN at work place to improve productivity and efficiency and cut
down analytical times.

4. TRAINING IN ABROAD:
Got trained in handling & trouble shooting of Skalar instrument during Feb 2011 Amsterdam, Holland.
ABOUT ME:
I am a thinking individual; clear and decisive, open to others' ideas, views and suggestions. The final decisions are products
of my thought process and hence my responsibility. Independence and freedom of thought brings out the creativity in me
and I live by the motto: "HONESTY IS THE BEST POLICY and THE TRUTH SHALL SET YOU FREE".
AIMS AND ASPIRATIONS:
In the next 5 years, I look forward to
1. A fulfilling career filled with exciting problem solving, client interactions, contributing to clinching business deals,
understanding customer needs and delivering the best.
2. A period of professional growth, encompassing work that stimulates the mind to think, generates questions, forges ideas,
culminating in solutions, in an environment conducive to give free reign to scientific thought.
3. A period of continuous learning from every project and every hurdle ultimately contributing to the growth of the
organization.
Reference
1. Mr. Muthu Krishna; Senior manager (SMV-QC) Biocon Ltd. Contact No-9845226589
2. Mr. Harish M Nayak; Manager(QC) Biocon Ltd. Contact No- 9901088337
EXTRACURRICULAR ACTIVITIES:
Represented biocon corporate cricket team in corporate level matches.
I do here by declare that the above information furnished details are true to the best of my knowledge and belief.
Place: Bangalore yours faithfully
Date: (Dharmendar B.S)