Pharma Formulation and Development : Resume

[Guest]

dear sir its my destiny work in formulation and development in pharmaceutical industry
I attach my c.v for that,

Name : Tejas Modi
Email :tejas_ankit AT yahoo.co.in

Job Objective :
Assignments in product Development/ Quality System Implementation, Production oriented with a high growth oriented organization.

Professional Synopsis :
- Offering 3 + years of experience in the areas of Production of Tablets and Capsule in area of Pharma field.
- Presently associated with Zydus Cadila Pharma Ltd Ahmedabad as production officer.
- Adept at developing formulas for necaw products at commercial scale production and ensuring its quality compliance.
- Excellent analytical, troubleshooting and inter-personal skills with proven ability in driving numerous quality enhancement, process improvement and cost savings initiatives during the career span.
- Result oriented, Presentation and Leadership skill
- Well versed with the production of Tablets like Metformin,simvastatin,paroxetine,and carvedilol

Academic Credentials :
- M.sc In pharmaceutical science from Greenwich University U.K in 2007
- B.Pharma from Shree S.K Patel Collage of Pharmacy Ganpat Vidhyanagar Mehsana in 2004

IT Skill Set :
- Window based software’s i.e. MS Office, utilization of other facilities.
- Familiar with SAP system.

Areas of Expertise :
Quality System Implementation
- Setting up facilities in the organization to spearhead quality management initiatives.
- Establishing Quality System across various processes to meet the pre-set quality standards and reduce rejection levels.
Product Development / Process Improvement / Productivity Improvement
- Ensuring complete in-process check and continuous improvement in process capabilities.
- Imparting training to all employees, pertaining to quality implementation and productivity improvement.
Documentation
- Preparing and maintaining documentation. i.e. BMR, SOP’s and other quality related documents
- Executing USFDA Documentation Maintaining & Creation.
- Reviewing SOP’s, technical specifications, qualification protocols, qualification reports and other quality documents.
- Implementing stringent systems to ensure high quality standards at all the stages of production.

Organizational Experience ::
Since2009 working in Zydus Cadila as an Executive.

Key Role Area :
- Steering initiatives towards handling of production related activities right from stage of Dispensing, Granulation, Compression, Coating and Inspection.
- Actively participated during USFDA audit.
- To assist investigation and market complains .So as to find out and correction actions.
Follow up for release and keep the batches ready as per belt wise packing plan on time.
- Establishing coordination with QA, QC, Stores & Maintenance Department for timely &smooth production activities.
- Work allocation to supervisory staff.
- Generation of new sops of new instrument & equipment as per cGMP.
- Handling shift schedule independently.
- Familiar with process validation and calibration

Highlights :
- Demonstrated abilities in achieving planned production within specified time limit with best quality parameters with minimum production losses.
- Suggested & implemented many improvement/modification in the process, machine & system to increase the productivity, improved quality, cost reduction & manpower saving.
- Increased the frequency of the Training Program me to the operators and juniors during USFDA Audit to increase awareness in quality.
- Dedication, Result Oriented, coordinating team activities.
- Proven ability to efficiently and adapting new technology.
- Conceptual thinking and adapting new technology.
- Dependable and flexible character, with inexhaustible stamina for work.
- Reviewing batch production and control records.
- Maintaining the records of Punch receipt, issue and return & destruction record.
- Generation of new sops of new instrument & equipment record.
- Planning of production targets as per firm plan.
- Handling manpower & machinery for Qualitative and Quantitative production in tablet Dispensing granulation, compression and coating.
- Responsible for all Tablet Department Activity.

June 2008 to July 2009 : IPCA Laboratories Ltd. Kandla as a Production Officer
Key Role Areas :
- Reviewing batch production and control records.
- Maintaining the records of Punch receipt, issue and return & destruction record.
- Generation of new sops of new instrument & equipment record.
- Planning of production targets as per firm plan.
- Handling manpower & machinery for Qualitative and Quantitative production in tablet Dispensing granulation, compression and coating.
- Responsible for all Tablet Department Activity.

Highlights :
- Actively involved in small group activity i.e. TQM training and got three star and four star project from CSC Mumbai.
Established capability to follow procedures and guideline.

Audit Exposure :
- USFDA, MHRA (U.K), TGA (Australia), WHO & Ukraine.
- MCC (South Africa), Brazil (ANVISA).

Personal Profile :
Name :Tejas Bharatbhai modi
Language Known :Hindi,English & Gujarati
Mehsana-2
Present Salary :3.79 Laces/per Annam

[usha rani guru]

Usha Rani Guru
Vapi, Gujrat Email :ushaguru AT ymail.com

CAREER OBJECTIVE :
- To Seek a challenging position that offers opportunity to explore my Qualification , Experience & skills in the area of Formulation & Development in such organizations that provides a work environment that foster teamwork and allows independent responsibilities.

WORK EXPERIENCE :
- 6 months experience as a trainee in BHABA ATOMIC RESEARCH CENTRE.
- Currently working as a F&D Executive in UMEDICA LABORATORIES PVT Ltd. Since 2ndJuly 2010 till date.

CURRENT JOB RESPONSIBILITY :
- To carry out formulation development and evaluation of Reference product..
- Conducting literature search by USP, BP, Martindale, Orange book & Patent Consultant.
- Conducting the Preformulation study for the product development.
- Conducting development trails of tablets capsules achieving desired dissolution profile and manufacturing the stability batches.
- Preparing MFR ,PDR & Stability protocol
- Providing technical support in the Commercial batches as an when required.

ACHIEVEMENT :
Qualified the GATE Examination with All INDIA Rank of 504.

SKILLS :
Instrument handling : Tablet Compression machine, Rapid Mixer granulator, Fluidized bed drier, Vibratory sifter , Double cone blender, PLM, Roche friabilitor, Disintegration apparatures., Multimill , Halogen moisture analyser.
Computer Skill : MS Office, Internet Browsing

PERSONAL STRENGTH AND ATTRIBUTES :
- Self Starter with Good Interpersonal Relation ship Skills.
- Persistent & Thoughtful in undertaking tasks with structured work habit.
- Self confident, flexible & Adaptable to a changing Environment focused.

PROJECT WORK :
- “Spectrophotometric Determination Of Ramipril & Amlodipine IN Pharmaceutical Dosage Form” in my B.Pharm.
- “Preparation & Evaluation Of Lyophilized Kit For Tc-99m Human Serum Albumin Microspheres” in my M.Pharm at Board Of Radiation Isotope & Technology, Bhaba Atomic Research Centre.

PROFESSIONAL QUALIFICATION :
COURSE BOARD SCHOOL /COLLEGE YEAR of passing& CGPA

M.Pharm(Pharmaceutical technology) Biju Patnaik university of techniology,Orissa Royal college of pharmacy & health sciences,Orissa 2010, 9.24
B.pharm Biju Patnaik university of techniology,Orissa Roland institute of pharmaceutical sciences, Orissa 2008, 8.0

ACADEMIC QUALIFICATION :
COURSE BOARD SCHOOL /COLLEGE YEAR of passing& %
Intermediate (science) CHSE Ramadevi Womens college,Orissa 2003, 58%
Matriculate ICSE St. Marys school, Orissa 2001, 76%

PERSONAL DETAILS :
Nationality : Indian
Fathers Name :Mr Abhina Guru
Birth date : 1st june 1985
Languages known : English , Hindi, Oriya
Martial status : Married
JAJPUR , ORISSA

DECLARATION :
I hereby declare that the above information is true with best of my knowledge & belief.

Date :
Place : USHA RANI GURU

[Guest]

JYESTA SAI PAVAN
Mail :pavanpharma1 AT gmail.com
CAREER CONSPECTUS :
A dynamic professional with 1 Year 9 months of experience in Regulatory Affairs.
CORE COMPETENCIES :
Regulatory submissions, Licensing and NOCs of Drugs, Samples and Trial Batches, Client servicing, Vendors Handling, MIS Maintenance.
CAREER CONTOUR :
SPANSULES PHARMATECH PVT LTD
Executive-Regulatory Affairs
2011 June Till date
JOB PROFILE :
LICENSING :
Export NOCs from CDSCO (Central Drugs Standards Control Organisation)
Applying for Test licence, Licence renewals, Loan licence, additional products, GMP, WHO GMP, Free sale certificates from State Licensing Authorities (DCA)
Import Licences from DCGI (Drug Controller General of India)
Food Licence from FSSAI (Food Safety Standards Authority of India)

SAMPLES & EXHIBITS :
Following up samples through coordinating with various departments viz QA, QC, Production and R&D and dispatching them as per customer specifications.
Vendor Management, Complaints handling, CAPA reports (Corrective and Preventive Action), MIS Maintenance and Feedback surveys to ensure compliance.
Analyses per se Assay and Dissolution of sample pellets using UV.
REGULATORY DOCUMENTATION :
Preparation and review of Open and Closed part DMF (Drug Master Files), CTD (Common Technical Documents) with in the stipulation of customer’s request.
Verification of Dossiers and Tech Packs.
SCHOLASTICS :
Completed M.Pharm in 2011 from Annamalai University, Tamilnadu with 7.5/10.
Completed B.Pharm in 2009 from Annamalai University, Tamilnadu with 6.76/10.
Completed Intermediate Bi.P.C in 2005 from Narayana Jr College, Ongole with 60.6%
Completed S.S.C in 2003 from D.R.R.M.M Govt High School, Ongole with 62%
ACADEMIC PROJECT :
B.PHARM : Anti-microbial activity of plant extracts (Plantarum Resimosa)
M.PHARM : Formulation and evaluation of pantoprazole sodium enteric coated tablets.
IT SKILLS :
Packages :
MS Office
Operating System :
Windows, DOS

PERSONAL DOSSIER :
Name : J. SAI PAVAN
Father’s Name : J.V. PRASADA RAO
Date of Birth : 01.05.1988
Gender : male
Marital status : Single
Religion : Hindu
Nationality : Indian
Personal Interest : Listening to Music & Reading books
Languages Known : English, Telugu, Tamil & Hindi
DECLARATION :
I hereby declare that the information furnished above is true to the best of my knowledge.
Date : JYESTA SAI PAVAN

[bunny2797]

Respected Sir/ Madam,
I take this opportunity to introduce myself. I am completed Master of Pharmacy with Pharmaceutics specialization in G. Pulla reddy college of Pharmacy (affiliated to OU Hyderabad), Andhra Pradesh in the academic year 2009-2011.(november)
I have keen interest to pursue progressive and intellectually fulfilling career by being a part of your esteemed organization. I have gained firsthand knowledge in formulation development and I did my project on formulation and evaluation of levocetrizine dihydrochloride with natural and synthetic superdisintegrants. I have interested in formulation research and development, regulatory affairs and quality assurance.
I will really appreciate if you can provide me an opportunity to work in your esteemed organization.
I am hereby enclosing my curriculum vitae for your kind persual.
Thanking you sir/madam
Yours sincierely
Y. Narendra
M.Pharmacy (Pharmaceutics)