www.astron-research.com Ltd Ahmedabad : FORMULATION RESEARCH

[muthukalee]

FORMULATION RESEARCH

Group Leaders/Research Scientists/Research Associates

Qualifications : M.Pharm/Ph.D.

Capabilities : Well acquainted with all activities pertaining to formulation development techniques, product development from literature survey, patent evaluation for product under development, stability studies, technology transfer and process optimization to get cost effective and quality formulations. Competent enough to design and develop various pharmaceutical dosage forms, give technical inputs for dossier preparations & product registration. Should have knowledge and exposure in NDDS, Euro, ANDA and other regulatory requirements.

ANALYTICAL RESEARCH

Group Leaders/Research Scientists/Research Associates

Qualifications : M.Sc./M.Pharm/Ph.D.

Capabilities : Thorough understanding and on-hand experience in Analytical Method Development, Validation and Stability Studies as per EU/US requirements. Having thorough knowledge of impurity profiling, dissolution profiling and stability studies for developed market. Should possess operational knowledge of sophisticated instruments like HPLC, GC, FTIR, LC-MS, etc. Essential to have exposure to regulatory audits like US FDA, MCC South Africa, MHRA UK, TGA Australia, ANVISA Brazil, etc.

About us :
Astron Research Limited, a leading IP oriented pharma contract research organization, is a fast growing Pharma Contract Research Organisation (CRO) with a strong quest to deliver best services to the rapidly growing Healthcare industry and has embarked its presence as a prominent global CRO.

Contact us :
Astron Research Limited
10th Floor, Premier House, Opp. Gurudwara,
Sarkhej-Gandhinagar Highway, Bodakdev,
Ahmedabad - 380054, Gujarat, India

Email : careers@astron-research.com
http://www.astron-research.com

[Guest]

Ruchir Shah (M.Pharm, DDRA)
Email : ruchirshah88 AT gmail.com Birth Date: 14/06/1988

Career Objective
A result-oriented professional seeking a Quality environment where my knowledge and experience can be shared and enriched, I am currently looking for a position in the industry that will challenge my skills and provide room for growth and advancement contributing to the best of my abilities.
Education
Post Graduation : MS Forensic Pharmacy (Pharmaceutical Analysis) 7.7/10
Institute of Research and Development, GFSU May- 2011
Subject studied : A) Impurities profile of drugs. B) Modern pharmaceutical analysis.
C) Pharmaceutical nano chromatography, separation and analytical technique. D) Research methodology. E) Fundamentals of Intellectual property, regulatory guideline. F)Pharmacovigilence
G) Risk management quality assurance and assessment.
Graduation : Bachelor of Pharmacy 72%
Sigma Institute of Pharmacy, VNSGU April 2009

Certificate : Diploma in Drug Regulatory Affairs (DDRA) 67%
Institute of Pharmaceutical Education and Research, Pune
Professional Skills
- Thorough knowledge of GMP and Regulatory guidelines like USFDA and CTD.
- Acquaintance in the preparation of Drug Master File, DMF error sorting and dealing with deficiency letters.
- Can assist in the preparation of registration dossier for drug product in the foreign country.
- Well acquainted with ICH guidelines on quality, safety and efficacy.
- Thorough in schedules and the forms pertaining to import, export, manufacturing and loan licenses.
- Knowledge of QA, QC, Validation aspects and Clinical trials.
- Knowledge of various grades of solvents as per their applicability.
Technical skills
- Measure the absorbance, transmittance and peak finding of the compound analyzed using UV Spectrophotometer (Jasco).
- Sample preparation and analysis of the functional groups to assist in the structure of compound using IR (Bruker, Perkin Elmer).
- Selection and preparation of mobile phase, Solvent to be selected, packing materials for the column and assay of the drug by using HPLC (Jasco).
- Able to analyse samples using GC-MS (Shimadzu).
- In depth practicality of MS office- Word, Excel, PowerPoint.
Projects Undertaken
- Nanopores in anticounterfeit packaging technique at Institute of Research and Development.
- Hydrogels : A controlled drug delivery system at Sigma Institute of Pharmacy.
Industrial Exposure
- 3 months training at West Coast Pharmaceuticals in QA and RA departments.
- Visited Torrent Research Center in the ADL and CMB departments.
Seminars, Workshops and Presentations
- Seminar on “Intellectual property” summit at Ahmedabad Management Association.
- Workshop on “Nano HPLC : Theory and practice” at Ahmedabad management Association.
- Poster on “Nano pores in Anti counterfeit packaging technologies” presented at “3rd Bangalore Nano international conference” on frontiers of nanotechnology.
Activities and Achievements
- Filed a Patent on “Anticounterfeit packaging technique”.
- Member of the Editorial board for the university news letter “NeosSol-The rising sun of new science”.
- Review paper on Anticounterfeit Packaging Technologies published in the International Journal JAPTR.
- Member of the Organizing Committee for the event “Myriad-Application of Nanotechnology in Model designing”.
Declaration
- I hereby declare that the above furnished information is true and to the best of my knowledge


Ruchir Shah

[Guest]

Resume :
MODI FORAM PANKAJKUMAR.
Email : fmodi24 AT gmail.com
forammodi AT ymail.com
Area of interest
Formulation and Development,IPR, Regulatory affair
OBJECTIVE
To apply my knowledge and skills of pharmacy into organization, work in an innovative and challenging environment to dedicate myself for work undertaken and utilize my efficiency at the my best to fulfill the organization’s requirements.
Education & Qualification :
Degree Name of collage & university Percentage Year of Passing
M. Pharm (Industrial pharmacy) Semester 4
S. K. Patel college of pharmaceutical education & research institute, Ganpat university 72.43 % April 2011
M. Pharm (Industrial pharmacy) Semester 3 S. K. Patel college of pharmaceutical education & research institute, Ganpat university 75.50% December 2010
M. Pharm
(Industrial pharmacy) Semeater 2 S. K. Patel college of pharmaceutical education & research institute, Ganpat university 72.80% June 2010
M. pharm (Industrial pharmacy) Semester 1 S. K. Patel college of pharmaceutical education & research institute, Ganpat university, 70% December 2009
B.Pharm Arihant school of pharmacy Uvarsad,Gandhinagar,
Gujarat University 70.42%
April 2009
HSC/Inter Science Stream GSHSEB, Gandhinagar 70% March 2005
SSC GSHSEB, Gandhinagar 89% March 2003
Achievement
- I have done 3 month training in viva laboratory after completion of B.Pharm.
- I have qualified GATE examination with 86.24 percentile.
- I have got certificate of excellence in poster presentation of 3rd Indian pharmaceutical association- student forum 2010 on topic “Future trend in pulsatile drug delivery system”
- My research paper was selected on topic “Formulation & evaluation of multiparticulate system of mesalamine in treatment of immflammatory bowel disease in 62nd IPC 2010.
- I have completed my 8 month project work on topic “Formulation, optimization & evaluation of fixed dose combination of moisture barrier film coated bilayer tablet of artesunate & amodiaquine hydrochloride” in formulation & development department of Lincoln pharmaceuticals Ltd., Khtraj, Ahmedabad under guidance of Dr. Priyal R. Patel &Mr. Jigar H. Patel during M.pharm semester 3 & semester 4.
Strengths :
- Positive attitude, Smart work, Good in team work

[Guest]

CURRICULUM VITAE
Piyush Rasikbhai Gaudani
E-Mail : piyush.gaudani AT gmail.com

Career Objective
I believe in myself and my willingness to work hard in right direction with proper attitude. I have confidence to tackle different situations. Success in professional life is of utmost importance to me. I am comfortable working in a group and discharging my duties to the very best of my ability and attain a position of responsibility in the organization.
Educational Qualification
Pursuing M. pharm ( PHARMACEUTICS) from NIMS UNIVERSITY ,JAIPUR
Qualification Name of the School/College Board/University Year of passing Percentage
M.Pharm-11 Nims institute of pharmacy, Jaipur NIMS University, jaipur 2011 waiting
M.Pharm-1 Nims institute of pharmacy, Jaipur NIMS University, jaipur 2010 65.66%
B. pharmacy N.R.Vekaria Institute of Pharmacy & Research Centre Saurashtra university 2009 60.79%
Higher Secondary A.P.Swaminarayan School.Gondal G.H.E.B 2005 60.00%
Secondary Shree Swaminarayan Vidyalaya.Una G.S.E.B 2003 71.29%
Project Work : (Zydus Cadila healthcare ltd. Ahmedabad)
“FORMULATION DEVELOPMENT AND EVALUATION OF SUSTAINED RELEASE COLON TARGETED ANTI-INFLAMMATORY TABLET”
Article Publication : (Journal of Global Pharma Technology)
“INSULIN DELIVERY : PRESENT AND FUTURE PROSPECTIVE ”
Seminar given on- Resealed Erythrocytes,
Soft Gelatine Capsule,
Drug master file,
Copy right.
IPC Attended- Attended National level seminar organized by 61st IPC in Nirama University,
Ahmedabad on December 2009.
Strengths
- Team spirit and adjustable nature
- Discipline and hard work
- Positive Attitude
- Time management, decision making power and enthusiastic
Area of interest :
- F&D
Hobbies

- Playing Chess
- Playing Cricket

[mrugank]

RESUME
Mrugank B. Parmar
Email : mrugank.b2 AT gmail.com


CAREER OBJECTIVE :

- To work for the challenging assignment that will provide me the opportunity to put my abilities towards growth in the respective field.
EXPERIENCE :
- I have an experience of 1 year for Preparation of Clinical Protocol & Submission of 1458 (1024 & 434) Adverse Drug Reactions (ADRs) cases to Peripheral Pharmacovigilance Center - GMCH at Guwahati Medical College and Hospital with its Detailed Scientific & Statistical Analysis as causality, severity, preventability & predictability assessment, from the Dept of Psychiatry at GMCH and Dept of Medical Oncology at Dr. B. Borooah Cancer Institute – Assam respectively, 2010.
AREA OF INTEREST :

- Pharmacovigilance – Drug Safety Associate
- Clinical Research
- Clinical Trials
- Regulatory Affair
- Medical Writing
- Pharmacokinetic
- Bioavailability & Bioequivalence Studies
Formulation & Development

ASSETS :
- Familiar with Industry-Standards such as ICH (USA, EUROPE, JAPAN) – GCP & Global Pharmacovigilance Guidelines provided by U.S.FDA (USA), CDSCO (INDIA) & ANVISA (BRAZIL).
- In more having familiar with Gold standards of Pharmacovigilance - MedDRA, WHOART, PSUR, CCDS, CCSI and FDA 21 CFR Part 11 etc.
- Having a good command on Scientific Medical Terminology.
- Shoulders are always enthusiastic to carry out the responsibilities and respect a venture to provide support to the Brand Safety Leader/Pharmacovigilance Leader (BSL/PVL) in the monitoring of the safety profile of assigned products including :
- Safety Update Report (PSUR),
- Risk Management Plan (RMP) updates and associated activities,
- Safety signal detection,
- Coordinating the management of large datasets for analysis purposes,
- Responses to external authorities,
- Review of clinical protocols and other regulatory activities, and
- Responsibility for the clinical review and evaluation of cases including input for follow-up and data cleaning, within agreed timeframes and to a high standard of accuracy, in compliance with IMS business rules, standard operating procedures and global and local regulatory requirements.
EDUCATIONAL QUALIFICATIONS :
- M.Pharm : M.Pharm in Pharmacy Practice from National Institute of Pharmaceutical Education and Research (NIPER) - GUWAHATI with Distinction - 8.04/10 CGPA (70.2 %), in the year of 2009-2011.
- B.Pharm : K. B. Institute of Pharmaceutical Education and Research (KBIPER), affiliated under Gujarat University with 60.25 % aggregate, Gandhinagar, in the year of 2005-2009.
- H.S.C : G.S.H.S.E.B. board with 86% merit, in the year of 2005.
- S.S.C : G.S.H.S.E.B. board with 88.71 %, in the year of 2003.
CREDENTIALS :
- Qualified NIPER - JEE exam in year 2009 and secured ALL INDIA RANK 434.
- Qualified GATE exam in year 2009 and secured 95.97 percentile, Governed by IIT Rorkee under Ministry Of Human Resource Department, Govt. of India
ADDITIONAL QUALIFICATIONS :
- Successfully accomplished a Distance learning Course on Intellectual Property Rights (DL-101), granted by WIPO, 2010.
- Successfully accomplished an online certification exam for “Clinical Research Training Programme” governed by National Institute of Health, US, 2010.
- Successfully accomplished an online certification exam for “Good Clinical Practice Training Programme” governed by PharmaXM School, UK, 2010.
PROJECT STUDY DURING M.Pharm :
1. A titled “Adverse drug reaction monitoring and drug drug interaction study at Psychiatry department of Guwahati Medical College and Hospital – Assam.” 2010.
2. A titled “Adverse drug reaction monitoring and drug drug interaction study at Medical Oncology department of Dr. B. Borooah Cancer Institute – Assam, 2010.”
LIST OF PUBLICATIONS :
1. Published a review article entitled "Assets of Pharmacovigilance, Its Necessity and Future in INDIA in coming five years." at Pharma Shine 2011 organized by Pharma Tutor, Available at http http://://www.pharmatutor.org/articl...lance-in-india
2. Published a case report entitled “A case of Neuroleptic malignant syndrome associated with olanzapine and responsive to bromocryptine.” at Scholars Research Library – Annals of Biological Research 2010; 1(4) :181-184.http://scholarsresearchlibrary.com/A...-4-181-184.pdf (accessed 31st December 2010).
3. Published a “Challenges facing Pharmacovigilance programmes in next ten years” review paper at national symposium on Pharmacovigilance, Sponsored and Coordinated by CDSCO, (pg no.62 - 64), 2010.
PRESENTATION DELIVERED :
- Poster presentation on “Neuroleptic malignant syndrome induced by olanzapine and awareness of adverse drug reaction monitoring”, 2010.
CONFERENCES/WORKSHOPS ATTENDED :
- National symposium on Pharmacovigilance, at GMCH, 17th march, 2010.
- Attended 61st “Indian Pharmaceutical Congress (IPC)” held at Nirma University, Dec, 2009.
- Attended 60th “Indian Pharmaceutical Congress (IPC)” held at New Delhi, Dec, 2008
INDUSTRIAL TRAINING :
- Indica Laboratory (P) LTD. in Analytical department, Ahmedabad, for six months 2008.
OMPUTER PROFICIENCY :

- Good in Microsoft Office package (MS word, Excel, Power Point).
- Scientific data retrieval from various Internet portals like Science direct, Pubmed, Medscape etc.
PERSONAL SKILLS :

- Excellent communication skill & Positive attitude.
- Good Coordinative in team work and can work independently too.
- Sincerity, dedication & loyalty towards work.
- Zeal to enrich my knowledge.
- Respect and abide to the rules of the Organization and culture.
- Enthusiastic to accept new venture for better opportunity.

[rajeev soni]

RAJEEV SONI
Email : rajeevsoni.bhu AT gmail.com
PRODUCT ASSIGNMENTS
~ Formulation Development ~ Process Development ~Product Development ~Project Management

PROFESSIONAL SNAPSHOT
A Formulation Development Pharmacist with around 7 years of experience in Formulation Development, Technology Transfer, Process Development, and Project Management presently designated as Senior Research Scientist in Product Development Research department with Ranbaxy, a renowned research based Pharmaceutical Company. Deftness in analysing existing processes, conducting the Lab/ Pilot scale up, and validation of new product. Demonstrated proficiency in dosage forms that include oral solid dosage, parenteral emulsions and dermatological formulations. Quality improvement of existing product, coordination with supporting department for new product launching activities with a chain of development scientists. Adept at business acquisitions, negotiations, contract development and strategic planning with an outstanding 'track record' of developing and implementing new procedures as well as taking cost saving initiatives. A keen communicator honed with managerial, relationship management, interpersonal, communication & problem solving skills.
Significant Attainments;
- Gathered skills in managing Formulation development Optimisation and scale up concerns of Conventional and extended Release Solid Orals, New Product Development, Validation Process, & Project Management as per the guidelines of Regulatory and Semi regulatory markets across the career.
Educational Status
- Qualified GATE 2003, scoring 99.01 Percentile with all India Ranking 61.
Examinations Institution/
University Year Main Subjects studied % of Marks Obtained
M.Pharm Institute of Technology,
Banaras Hindu University 2005 Pharmaceutics, Biostatistics, Biopharmaceutics and Clinical Pharmacokinetics, Novel Drug Delivery System, Dissertation Work 81.2%
B.Pharm Rajiv Gandhi University of Health Sciences, Karnataka 2002 Pharmaceutics, Pharm. Chemistry, Pharm. Analysis, Pharmacognosy, Pharmacology, Pharm. Microbiology, Forensic & Community Pharmacy, Biochemistry, Dispensing, Hospital and Clinical Pharmacy 60.6%
Diploma in Total Quality Management &
ISO 9000 Indian Institute of Management & Technology (IIMAT), Chennai 2002 Total Quality Management 74%
Diploma in Business Organization and Management IIMAT, Chennai 2003 Business Management 71.5%
International Research Publication
- In Vitro and in Vivo Evaluation of Buccal Bioadhesive Films Containing Salbutamol Sulphate, Chemical and Pharmaceutical Bulletin, 58 (3) 307-311, March 2010.
Core Competencies
- Good understanding of quality based ICH guidelines, module 2 and module 3.
- Effective coordination with team by educating stringent means for routine product development activities.
- Coordination with Marketing for getting New Product Development Request in a specified format.
- Preparation of technical write-up required for form 12, form 44 for new formulations.
- To give technical support to regulatory affairs department in solving country specific product related queries.
- Coordination with Purchase and Production Planning Inventory Control (PPIC) regarding procurement of raw materials (Active along with Technical Package and Vendor COA, Inactives along with vendor COA), packing materials along with COA and miscellaneous materials (Tools : punch sets, packaging change parts as per physically evaluated market samples or other In-House product development strategies). Getting raw material and packing material code generated by PPIC department under timely authorization by QA.
- Getting raw materials and packing materials tested by In-House Analytical Testing facility. Getting In-House COA generated accordingly.
- Coordination with QA-Validation and Engineering departments for obtaining IQ/OQ/PQ reports of every machine and instruments in the premises of F&D department. Monitoring calibration of every instruments on timely basis.
- Good understanding of literature survey along with Patents relevant for desired formulation development.
- Good understanding of preformulation studies, formulation development trials, dissolution medium selection criteria, analytical (Assay, Dissolution, Related Substances) method validation work, comparative product characterization, ICH compliant stability studies in proposed/ alternative market pack and understanding of Bioequivalence (Pilot/Pivotal) studies.
- Coordination with Packaging Development department and getting generated related Master Documents (Master Packing Card, Foil Artwork, Insert Artwork, Label Artwork, Carton Artwork).
- Good understanding of Technology Transfer Documents (Test License, Pharmaceutics Development Report, Master Formula Card, Master Packing documents, Raw Material Specifications, Finished Product Specifications (Release and Regulatory), Standard Analytical Test Procedures, Stability Reports).
- Good understanding of trouble shooting, as and when required, by analyzing process parameters of different manufacturing and packaging stages.
Career Highlights
Lupin Limited, Mandideep February 02-- January 03
- Traineee Officer (Process Development-Formulation).
- Dossier review, arrangement and adequate availability of all relevant documents (Master Formula Card, In-Process, Product Release and Regulatory Specifications, Raw Material (API and Excipients) Specifications, Stability Protocols).
- Execution and Subsequent technology transfer of Oral and Sterile (Dry Powder for Injection) Cephalosporins Products pertaining to Advanced and Domestic Markets in USFDA, UKMHRA approved formulation manufacturing unit.
- Ascertaining feasibility of trials and tooling development. Trouble shooting and route cause analysis.
- Preparation of Manufacturing and Packing Batch Production Records (Intended/ Commercial/ Hospital Supply) pertaining to Domestic and Export Markets of Oral and Sterile Cephalosporin Products.
- Preparation of Test Batch Monitoring, Process Validation Protocols, Stability Study Protocols, Hold Time Study Protocols and Compilation of Test Batch Monitoring, Process Validation, Stability Study, Hold Time Study Reports of Oral and Sterile Cephalosporin Products and other Reports of Experimental Batches conducted by Process Development Lab from time to time.
Reason for leaving : Joined M.Pharm course of prestigious IT, BHU on UGC Fellowship
Alkem Laboratories Ltd., Mumbai September 05-- February 07
- Research Associate (Formulation & Development)
- Was responsible to develop, scale-up, and validate commercializable robust products for US Market. Trouble shooting for process and products. Support stability group. Review and analyze stability data. Evaluation of new and alternative raw materials. Develop rework procedures. Preparation of CTD for US market.
- Worked in solid dosage forms such as Sustained release tablets, Conventional tablets, Enteric coated tablets for Advanced Markets
- Process development ; characterization, ranging and optimization; Facilitate Transfer of Technology (New products) ; Provide validation support for product site transfer ; Process audit, Identify process / product anomalies and address process deviations, regulatory guidance to internal partners.
Cadila Pharmaceuticals Ltd., Ahmedabad February 07 -- January 08
- Research Associate (Formulation & Development)
- Preparation of CTD (Module 2 & Module 3) for two projects US market.
- Patent drafting for a project intended for Australia.
Troikaa Pharmaceuticals Ltd, Ahmedabad January 08 --January 11
- Joined as Sr. Manager and promoted to the level of AGM (Formulation & Development)
- Was responsible for the formulation development team of 6 Scientists to develop NDDS (Dermatological formulations, Parenterals, solid oral dosage forms); Project Tracking and coordination (Technical) for New Product Development; Key member in Approval for DSIR of R&D centre Pharma Division. Responsible for technology transfer of Products; Project management of contract research project (FDA Classification Type 3); Coordinating with packaging development, procurement, Analytical, Costing, Marketing, Patent Cell, medical services, Production for both New Products and Site Transfer; Budgeting and Budgetary control.
- Demonstrated proficiency in generation and compilation of data required for quality overall summary and module 3, intended for EU, for a very commercially successful patent on injectable formulation. Also involved in effective coordination with Medical Services department regarding compilation of data concerning Non-clinical study reports and clinical study reports.
Ranbaxy Laboratories Ltd, Gurgaon
- Presently working as Senior Research Scientist in Product Development & Research department with Ranbaxy, a renowned research based pharmaceutical company.
Job Profile
- Formulation and Development for API source variation projects intended for Advanced Markets.
- Formulation and Development for harmonization activities intended for emerging markets
- Formulation and Development related documents preparation for dossier filling intended for Rest of African countries.
- Query response for filled dossiers.
Achievements at Ranbaxy.
- Successfully completed API source variation projects for Brazil and USA to meet timely production requirements.
Instrument/Machine Skills
- Experience in understanding instruments and machines like Silverson Homogeniser, Emulsiflex 160 Homogeniser, Sterile manufacturing tank, filtration tank, sterilization & depyrogenation tunnel, Compression machine, Rapid mixer granulator, Fitz Patrik® Roll compacter, Fluidised bed drier, Multimill, Supermill, , Planetary Mixer, Vibrosifter, Auto Coater with PLC, Brookefield Viscometer, Ultrasonicator, UV Spectrophotometer, IR moisture analyser.
Computer Skills
- Operating Systems : MS- DOS, MS-WINDOWS
- Working Knowledge of SAP, Documentum Compliance Manager

References
- Shall be made available on request
Notice Period
- One month or subject to relieving by present employer whichever is earlier.

[Guest]

CURRICULUM VITAE
VISHNU SHANKAR NAYAK
E-mail id- vishnushankar.nayak AT gmail.com
CAREER OBJECTIVE :
To grow in a conducive environment exploring my domain and potential to the fullest, and attain the ultimate objective of the organization where I can prove my caliber and nevertheless be a good team facilitator.
PROJECT TITLE :
- “Formulation and Evaluation Of Fast Dissolving Buccal Film of Ondansetron Hydrochloride and Compared with Fast Dissolving Tablet Of Ondansetron” from R.K.I.G.T, Ghaziabad.
EDUCATIONAL CREDENTIALS :
QUALIFICATION BOARD/UNIVERSITY YEAR OF PASSING % OF MARKS
M.Pharm(Pharmaceutics) U.P.T.U Lucknow 2011 74.66
B.Pharm R.G.P.V Bhopal 2008 73.00
ISC M.P.Board 2003 60.23
HSC C.B.S.E 2001 70.02
RESEARCH PAPER
Research paper has been communicated to The Journal of Pharmaceutical Development and Technology.
KEY SKILLS :
- Internet : Information searching and retrieval using various medical search engines viz. Google scholar, Sciencedirect, Pubmed, HighwirePress, Scifinder
- Knowledge of working on various computer software viz. Microsoft Office package
FIELDS OF INTEREST :
- Research & Development
- Regulatory Affairs
- Formulation & Development
INDUSTRIAL TRAINING :
- Worked as trainee for a period of 30 days at Lupin Limited, Mandideep Bhopal.
EXTRA CURRICULAR ACTIVITIES :
- Participated in The Hospital Pharmacist Association, Meerut U.P.
- Participated in workshop on Nanomaterial Recent Techniques and Application at Shobhit University Merrut.
- National seminar on Recent Trend in Pharmacy Education and Practice Held at Vigyan Bhawan, New Delhi.
- National Conference on Innovation in Pharmaceutical Sciences in SGIT Ghaziabad (U.P)

[Guest]

ABIKESH PRASAD KUMAR MAHAPATRA
Email - abikesh_mahapatra AT yahoo.co.in
OBJECTIVE
To secure a position that will enable me to use my strong organizational skills, educational background and ability to work well with people and the best possible extent to grow professionally with your organization.
EDUCATIONAL QUALIFICATION
M.Pharm (Pharmaceutical Technology) : Biju Pattanaik University of Technology, Rourkela, in 2010 securing 9.5 percentile out of 10.
B.Pharm : Biju Pattanaik University of Technology, Rourkela, in 2008 securing 8.2 percentile out of 10.
MBA : North Orissa University, Mayurbhanj (Pursuing).
Advanced DIPLOMA in Drug Regulatory Affairs and Drug Designing : Pharma Help line Society, Jaipur, Rajasthan.
ACADEMIC PROJECT
M.PHARM PROJECT
Formulation, Development and Evaluation of In-Situ Nasal gel of Sumatriptan Succinate.
B.PHARM PROJECT
Improving Drug Solubility by using Solid Dispersions.
ACADEMIC ACHIEVEMENT
I have qualified GATE in the year 2008 with (All India Rank : 1183), Securing 95.62 percentile and received JRF by AICTE, New Delhi.
I have successfully qualified the WIPO World wide Academy’s Distance Learning course, “General Course On Intellectual Property DL-101”
WORK EXPERIENCE
March 2010 to July 2011 – worked as F&D officer in ANKUR DRUGS AND PHARMA Ltd, Baddi, Himachal Pradesh.
July 2011 to Till Date – Presently working as F&D officer in ARISTO PHARMACEUTICAL Pvt. Ltd, Mandideep, Bhopal, Madhya Pradesh.
AREA OF INTEREST
Formulation Research and Development (FR&D)
JOB PROFILE
- To carry out formulation, development & evaluation of innovator product.
- Literature search by USP, BP, Ph.Eur., Martindale, Orange Book, Patent Consultant.
- Conducting Preformulation studies of both Innovator & Generic product.
- Handling trial batches of Tablets, Capsules, Liquids, Dry Syrups and analyzed their physical properties in both R&D and Manufacturing area.
- Preparing MFR, BMR, Product Development Report (PDR) & Stability Protocol.
- Development of formulation related to low RH Products.
- Deft in organizing day to day research activities and executing tasks as appropriate to the timely accomplishment of research objectives.
- Very much acquainted with taking scale up batches.
COMPUTER SKILL
Expertise in MS Windows, MS Word, MS Excel, MS PowerPoint, MS DOS and Internet Application.
LIST OF PUBLICATION
1. Anjan K. Mahapatra , P. N. Murthy ,Sudarsan Biswal, Abikesh P.K.Mahapatra, Siba P. Pradhan , “Dissolution Enhancement and Physicochemical Characterization of Valsartan in Solid Dispersions with ß-CD, HP ß-CD and PVP K-30”, Dissolution Technologies, February 2011,Volume 18,Issue-1.

[Unregistered]

CURRICULUM VITAE
ASODIYA HARSHADKUMAR VINAYKANT
B.Pharm, M.Pharm (Pharmaceutics)
Email harshadasodiya AT gmail.com

CAREER OBJECTIVE :
To start career with an organization that provides excellent job opportunity and which enables me to apply my skills to achieve best organizational objectives.

PERSONAL DETAILS :
Name Asodiya Harshadkumar Vinaykant
Date of Birth 17/12/1989
Nationality Indian
Gender Male

EDUCATIONAL DETAILS :
EXAMINATION MON/YEAR OF PASSING BOARD/
UNIVERSITY MARKS OBTAINED OUT OF PER/SPI
S.S.C. MARCH2005 G.S.E.B 553 700 79.00%
H.S.C. MARCH2007 G.S.H.E.B 451 650 68.20%
1st B.PHARM MAY2008 SAURASHTRA UNI. 663 1300 51.00%
2nd B.PHARM APRIL2009 SAURASHTRA UNI. 802 1300 61.69%
3rd B.PHARM APRIL2010 SAURASHTRA UNI. 727 1200 60.58%
4th B.PHARM APRIL2011 SAURASHTRA UNI. 892 1400 63.71%
M.pharm (sem1) FEB2012 GTU 7.4 SPI 10 SPI 7.40
M.Pharm (sem2) SEP2012 GTU 7.0SPI 10SPI 7.00
M.Pharm (sem3) MAR2013 GTU 7.57 SPI 10 SPI 7.50
M.Pharm (sem4) Thesis accepted GTU Awaiting for Result

I had completed my B.PHARM from C.U.SHAH COLLEGE OF PHARMACY AND RESEARCH, which is affiliated to Saurastra University & school from Girdharnagar higher secondary school affiliated to G.S.H.S.E.B. board.
Aggregate of the B.Pharm : 62.41%

COMPUTER AWARENES :
M.S. Office

TECHNICAL COURSES KNOWN :
Internet
TRAINING PROFILE :
1 Month industrial training in ZYDUS CADILA.
3 Month industrial training in SUNIJ PHARMA.
6 month Industrial Project on “Formulation and Development of Mouth dissolving Tablets of Amlodipine Besylate in LINCOLN PHARMACEUTICAL LTD, Ahmedabad.

ACHIEVEMENTS :
Poster presentation in SARSWATI COLLEGE OF PHARMACY & S.K.PATEL COLLEGE OF PHARMACY on ARTIFICIAL BLOOD.
Poster presentation in A.R.COLLEGE OF PHARMACY, VIDHYANAGAR, ANAND.
Attended National level seminar in BABARIYA COLLEGE OF PHARMACY,BARODA.
As a coauthour in paper publication, NOVEL APPROACH : CHEWING GUM in IJPRD Journal.
As a Author in Research Paper Publication, in IJPRJ JOURNAL (Formulation and Evaluation of diclofenac sodium Floating Tablet by Melt granulation Technique.)

PROFESSIONAL PROFILE :
Highly organized and dedicated, with a positive attitude.
Ready to accept challenge from surrounding to achieve the best.
Believe in perfection in everything.
Gives the best of myself.
Have excellent interpersonal communication skills.
Eager to learn regarding new technologies.
Doesn’t get afraid of losing.

HOBBIES :
Playing badminton, internet surfing and other outdoor games.
Singing songs,& play loud rocking music.
Reading novels, books & different articles.

[Unregistered]

Suman. A. Tripathi
E-Mail : suman2480 AT gmail.com

OBJECTIVE :
To Associated with a progressive organization that give me the scope to apply my knowledge & skills & also involve myself as a part of the team that work toward the growth of organization

EDUCATION QUALIFICATION :
COURSE INSTITUTION SECURED YEAR
S.S.C Pragati Hindi High School Gujarat Board 70.20% Dist 2005
H.S.C Seth C.L Hindi High School Gujarat Board 60.63% First 2007
B.Sc (BOTANY) Gujarat University 66.6% First 2010
M.Sc (BIOINFORMATICS) Gujarat University 67.6% First 2012

RESEARCH PUBLICATION :
Published my book “Normal and binding mode analysis of breast cancer resistance protein”. Alina Covali (Ed), LAP LAMBERT Academic Publishing GmbH & Co. KG, Saarbrucken, Germany, ISBN : 978-3-659-15312-9.

PROJECT WORK :
Investigation of ligand Binding in Breast Cancer Resistance Protein (BCRP) towards developing Resistance using computational methods.

RESEARCH AREA OF INTEREST;
1. Melecular Modelling
2. Sequence Anlaysis
3. Docking
4. Durg Desginging
5. In Vitro & In Silico Analysis
Academic Award
Best poster award (First prize) for “My Dream To Conquer Cancer” in one day Seminar on “Cancer” as a part of National Science Day Celebration-2013 organized at the Gujarat Cancer & Research Institute Ahmedabad

ABSTRACT PUBLICATION & POSTER PUBLICATION :
Poster Presented in the National Symposium on Evolving Paradigm to improve Productivity from Dynamic Management & Value Addition for Plant Genetic Resources organized by Department of Botany, University School of Science, Gujarat.
TRIPATHI SUMAN A, SHETTY SHILPA S. NEXT GENERATION SEQUENCING IN ARABIDOPSIS THALIANA PLANT GENOME in the National Symposium on Evolving Paradigm to improve Productivity from Dynamic Management & Value Addition for Plant Genetic Resources organized by Department of Botany, University School of Science, Gujarat.
Suman A Tripathi, Shiva Kumar Prashant Kumar, Himansu A Pandya , Yogesh T Jaisrai INVESTIGATION OF LIGAND BINDING IN BREAST CANCER RESISTANCE PROTEIN TOWARDS DEVELOPING RESISTANCE USING COMPUTATIONAL METHODS in XXVII Gujarat Science Congress at Charotar University of Science & Technology Changa.
Also Presented poster at XXVII Gujarat Science Congress at Charotar University of Science & Technology Changa on Breast Cancer.
Participating in state level Seminar on “Innovative Approaches to Biological Science Recent Prospecting organized by Department of Biology J.& J College of Science Nadiad.
Presenting poster in The Vignan Parishad the Science Excellence-2011 on GENE MAPPING.
Presenting Poster in BIOINFO CONCLAVE 2013 National Seminar on MD Simulation & QSAR In Drug Design Held on 29th Marh At GCRI Ahmedabad.

ATTENDED SEMINAR & WORKSHOP :
National Symposium on Evolving Paradigm to Improve Productive from Dynamic Management and Value Addition for Plant Genetic Resources.
Healthy environment for Youth.
Intellectual Property Rights Awareness.
Advance training on Bio-Computational statistics
Bioinfo Conclave- National seminar on Bioinformatics in High-throughput Era

BIOINFORMATICS SKILLS :
Programming Languages : C-lang, Java/Basic
Scripting Languages : Perl, Java/Basic
Database Development : MySQl
Database : NCBI, EMIBOSS, EXPASY, SWISSPROT, PIR, PDB,
GENOME BROWSER & all prominent Bioinfo database.
Molecular Docking : Mole grow, Argus lab, IGEMDOCK.
Protein Modeling : Homology modeling, Swiss Model, Pyre2 server.
Sequence Alignment : BLAST, FASTA, Clustal W, Clustal X.
Energy Minimization : YASARA
Structure Manipulation : YASARA, Rasmol, Spdv, & other offline & online tool
Structure Verification : SAVES, RAMPAGE.
Pharmocophore Analysis : Ligand Scout.
Molecular Dynamics : VMD, NMA, Felx Server.
Phlyogenetics Analysis : MEGA PACAKGE, PHYLIP PACAKAGE.

PERSONAL PROFILE :
Date of Birth : 7th May 1989
Father Name : Ajitkumar. V. Tripathi
Marital Status : Unmarried
Religious : Hindu/Brahmin
Email Id : suman2480 AT gmail.com
Nationality : Indian
Languages known : Hindi, Gujarati, English

REFERENCES :
Dr.Y.T Jasrai
Professor & Head
Bioinformatics Coordinator
Gujarat University Department Of Botany
School Of Science
Ahmedabad Dr. H.A Pandya
Professor & Coordinator
Department of Botany
School of Science
Gujarat University
Ahmedabad

DECLARATION :
I hereby declare that the above data presented is true to the best of knowledge and can be supported by necessary certificates for your ready reference.

Place : Ahmedabad
Suman A Tripathi

[Unregistered]

Respected Sir/ Ma’am, company
I under signed Tarang S. Shah. a student perusing M. Pharma in Clinicla Pharmacy, from KLEUs college of Pharmacy, Belgaum. I am at the end of my academic year as well as my Post Graduate Degree.

I am having exposure to clinical activities and played different role as a clinical pharmacist which are mentioned below.

Role as Clinical Pharmacist :
Ward round participation with Physicians (Medicine, Surgery, Pediatric)
Patient Counseling (Drug, Disease and life-style modification)
ADR reporting (Regional Pharmacovigilance Centre)
Prescription Analysis (appropriateness and rationality)
Case presentation and discussion
Drug information (Physician, MD student)
Handling of clinical trials

Other than clinical pharmacist I have exposure to Phase 3 and 4 clinical trials in different national and international company and played a role as a clinical research coordinator (CRC). The details are mentioned below.

Clinical Trial Exposure :
S.No Clinical trial area Designation Trial
Design Phase Experience
1 DVT Trial CRC RCT III 2011 Onwards
2 Diarrhea Trial CRC RCT III 2011 Onwards
3 Hypertriglyceride Trial CRC RCT III 2011 Onwards
4 Liver Cirrhosis Trial CRC Observational Study IV 2011-2012

I would like to apply for a job in your company, and work in the field of clinical research and to provide a batter patient care with the excellent work and enthusiasm. More details are mentioned in the CV attached in the mail.
I would welcome the opportunity to meet you and discussion my ideas for working in your company. I am looking forward to hearing from you soon.

Thanks and Regards.
Tarang S. Shah.
Clincila Pharmacist.