Jamjoom Pharmaceuticals Company Ltd Saudi Arabia : Chemist

[mskavi]

Jamjoom Pharmaceuticals Company Limited Saudi Arabia : QC,AMD,F&D,QA,Validation-Chemist/Microbiologist/Production Technician

Designation: QC,AMD,F&D,QA,Validation-Chemist/Microbiologist/Production Technician
Experience: 5 - 10 Years
Location: Saudi Arabia

Job Description:
Chemist – Analytical Method Development
1. Development and validation of analytical methods for the raw materials, finished products for Soft Gelatin capsules products including multi-vitamins and trace element formulations as per ICH guidelines.
2. Prepare dossiers for registration including all analytical profiles and reports.
3. Execute technical development related to soft gel development.
4. Analytical Instrument Calibrations, maintenance and qualification.

Production Supervisor - Soft Gelatin Encapsulation & Packaging Machine
1. Operation and maintenance of PHARMAGEL, ITALY make soft gel encapsulation machine.
2. To perform & supervise manufacturing activities as per cGMP requirements for soft gel capsules.
3. To prepare & supervise medicament and gelatin manufacturing.
4. To guide a team of technicians, troubleshooting of machine problems and to ensure smooth operations to meet the production demands.

Pharmacist – Formulation Development Soft Gelatin Capsules
1. To design, development and execute experiments leading to soft gelatin drug product development as per regulatory guidelines.
2. To maintain documentation and dossiers for regulatory filings for the registration of products.
3. To coordinate internal departments and external organizations for all F&D activities, management of the lab activities.
4. To prepare technical reports and technology transfer.
5. Trouble shooting of problems related to formulations of soft gelatin capsules like multi-vitamins, trace elements, etc.

QUALITY CONTROL – CHEMIST
1. Analysis of Raw materials / Bulk / Intermediate / Finished Products / Stability samples using Chemical and instrumental Methods.
2. Preparation of Test procedures, Specifications for Raw materials / Bulk / Intermediate / Finished Products / Stability samples.
3. Preparation of Standard Operating Procedures
4. Operation, Use, maintenance, validation and calibration of analytical instruments.
5. cGMP / GLP Compliance in QC Laboratory
6. Documentation as per cGLP.
7. Compliance with USFDA, MHRA, TGA, EU requirements for testing in a Quality Control Laboratory.
8. Maintain inventory and records for chemicals, spares, columns.
9. Willing to work in Night shifts on continuous basis.

QUALITY CONTROL – MICROBIOLOGIST
1. Analysis of Raw materials / Bulk / Intermediate / Finished Products / Stability samples using microbiological methods
2. Performance of Environment monitoring, trending and record maintenance.
3. Preparation of Test procedures, Specifications for Raw materials / Bulk /Intermediate / Finished Products / Stability samples.
4. Preparation of Standard Operating Procedures
5. Operation, Use, maintenance, validation and calibration of testing instruments.
6. cGMP / GLP Compliance in QC Laboratory
7. Documentation as per cGLP.
8. Compliance with USFDA, MHRA, TGA, EU requirements for testing in a Quality Control Laboratory.
9. Maintain inventory and records for media, chemicals, spares, glassware.
10. Willing to work in Night shifts on continuous basis.

VALIDATION & QUALITY ASSURANCE - EXECUTIVE / MANAGER
1. To perform all activities related to quality assurance like documentation control, SOP writing, review of documents for correctness and compliance.
2. To conduct internal and external audits, vendor assessments.
3. To perform process validation, analytical and instrument qualification and validation documentation and reviews.
4. To review all stability reports and validation, regulatory documentation.
5. To handle all OOS/OOT, CAPA and QMS systems, review of batch records, Annual Product reviews, PSQRs.

Desired Candidate Profile:
INTERESTED APPLICANTS MUST BE WILLING TO RELOCATE TO JEDDAH, SAUDI ARABIA IMMEDIATELY AFTER APPOINTMENT AND VISA STAMPING.

Chemist – Analytical Method Development
Ideal candidate should have B Pharm or Masters Degree in Science (Chemistry) or equivalent with 5 years hands on experience in Analytical method Development of Soft Gelatin Capsule with exposure to USFDA / EU / MHRA documentation.
Well versed with computer skills, HPLC, GC, AAS, Dissolution, FTIR, Calibration of instruments,Software validation. Ability to work in teams.
Production Supervisor - Soft Gelatin Encapsulation & Packaging Machine
HSC / Diploma in Pharmaceutical or technical / engineering with experience on PHARMAGEL, Italy make encapsulation machines for soft gel capsule manufacturing and UHLMANN, Germany make packaging machines. Hands on experience of above 5 years and able to trouble shoot machine problems – mechanical and electronic.
Pharmacist – Formulation Development Soft Gelatin Capsules
B. Pharma or M. Pharma and above with 5+ years or a Masters degree with equivalent experience (9+ yrs) within the pharmaceutical industry directly working with the development of soft gel dosage forms.Qualified candidates must have direct experience with the full development process from pre formulation, formulation development through scale-up. This is currently a hands-on laboratory development role, but the ideal candidate will have the leadership and project management skills to eventually lead others. Excellent interpersonal skills and oral and written communication skills are required.

QUALITY CONTROL - CHEMIST
Ideal candidate should have B Pharm or Masters degree in Science(Chemistry) or equivalent with 3 years hands on experience in quality control testing of raw materials, finished goods, in a quality control / quality assurance department of a
USFDA approved company for formulations or MNC.Well versed with computer skills, HPLC, GC, Dissolution, FTIR, Calibration of instruments,Software validation.USFDA, MHRA, EU requirements for QC testing and quality systems.

QUALITY CONTROL -MICROBIOLOGIST
Ideal candidate should have Masters Degree in Microbiology or equivalent with 3 yearshands on experience in MICROBIOLOGICAL TESTING in quality control testing of raw
materials, finished goods, in a quality control / quality assurance department of a USFDAapproved company for formulations or MNC
Well versed with computer skills, Pharmacopoeial testing of formulations, culture maintenance, Calibration and validation of instruments, Environment monitoring. Testingof sterile formulations. Identification of micro-organisms.

VALIDATION & QUALITY ASSURANCE - EXECUTIVE / MANAGER
Ideal candidate should have B Pharm or Masters degree in Pharmacy / Science(Chemistry) or equivalent with 5 years hands on experience in a quality assurance department of a
USFDA approved company for formulations or MNC. Well versed with computer skills, process validation, documentation, instruments,Software validation. USFDA, MHRA, EU requirements for quality systems.

FOR ALL POSITIONS:
Yearly return air ticket for home country with one month leave.
Visa will be arranged by the Company including all the cost for the Visa Application.
Age Limit : Below 35 years.
Experience: 5-15 years

Address:
Jamjoom Pharma
P. O. Box 6267 Industrial City Phase 5
Jeddah, Fax Number-6081222
Jeddah,Other,Saudi Arabia 21442

Email Address: cv@jamjoompharma.com
Website: http://www.jamjoompharma.com

Keywords: Soft Gelatin Capsule Quality Control Assurance Production Maintenance Chemist Executive Manager Validation GMP USFDA EU Analytical Pharmacist Microbiology Gulf Pharmaceutical R&D Tablet drug regulatory technician supervisor assistant PHARMA ICH GLP

[Guest]

SARFRAZ. MAMADAPUR
Email : sarfraz_ahmed106 AT yahoo.com

OBJECTIVE :
To be involved in service of people through best of my knowledge & skills in “Pharmaceutical field” as Healthcare Professional & establish working partnerships with healthcare professionals.
PERSONAL SUMMARY :
An enthusiastic, dedicated and hard working person with an outstanding academic background and excellent attitude to work. Highly motivated, reliable with a real passion for healthcare and the ability to develop and grow as a health professional.
ACADEMIC QUALIFICATIONS :
2007-2010 : Bachelor of Pharmacy.
Acharya & B. M. Reddy College of Pharmacy.
(Soldevanahalli, Hesaraghatta Road, Bangalore 560 090)
- Second year - 75.5% (Distinction)
- Third year – 80.5% (Distinction)
- Final year – 77.8% (Distinction)
2004-2006 : Diploma in Pharmacy.
Acharya & B. M. Reddy College of Pharmacy.
(Soldevanahalli, Hesaraghatta Road, Bangalore 560 090)
- First year – 77.7% (Distinction)
- Second year – 78.2% (Distinction)
2002 – 2004 : Pre-university College.
B.N.E.S College.
(Mahalaxmi Layout, Near Iskon Temple, Bangalore)
- First year – 60.3%
- Second year – 61.6%
2002 : S.S.L.C
Sri Vidya Kendra.
(Sri Muneshwara Education Society, Peenya 1st Stage, Bangalore 560058)
- Class 10 – 77.7%

WORK EXPERIENCE :
Dec 2010 – till present : Remidex Pharma Pvt. Ltd (Manufacturing of GSK products)
(B-249/B-250, 2nd stage, Peenya Industrial Estate, Bangalore 560058, India)
Job Title : Quality Assurance
Responsibilities :
- Checking Quality of all the Drugs manufactured in industry.
- Maintaining documents of all the drugs.
Nov 2010 – Dec 2010 : Columbia Asia hospitals Pvt Ltd.
Job Title : Hospital Pharmacist
Responsibilities :
- Contacting and working closely with other healthcare professionals.
- Checking prescriptions for errors & making sure they are appropriate for patients.
- Accurately dispensing drugs to patients according to a doctor’s prescription.
- Instructing patients on how to use medications, possible side effects and storage.
Nov 2006 – Nov 2007 : Ravi Kirloskar Memorial Hospital.
(No. 19, 2nd main road, 1st phase, peenya industrial area, Bangalore 560058.)
Job Title : Hospital Pharmacist
Responsibilities :
- Dispensing drugs to patients according to a doctor’s prescription.
- Measuring, packaging and labelling medications issued to patients.
- Re-shelving pharmaceutical stocks.
ACHIEVEMENTS :
- Attended Seminar on Clinical research conducted at our college.
- Attended Seminar on Community Pharmacy conducted at our college.
- Attended Conference Held by Indian Pharmaceutical Association at Acharya & B.M. Reddy college of Pharmacy, Bangalore.
- Participated in polio vaccination health camp held in Bangalore.
- Actively participated in blood donation camp held in Chennai.
EXTRA CURRICULUM ACTIVITIES :
- Actively participated in debates, dramas, quiz & essay competition held in school and college.
- Participated in Poster Presentation in college.
- Assisted in organizing various programmes in college.
- I like to involve in playing various sports.
KEY SKILLS AND COMPETENCIES :
- Microsoft Office. (Word, Excel, Power point)
- Keeping up to date with developments in the pharmaceutical industry.
- Able to work on tasks individually or as part of a team
- Excellent organisational skills that allow me to multi task effectively.
- Proven ability to understand problems and then develop imaginative and inventive solutions.

[Guest]

CURRICULLUM VITAE
Hutesh Ashok Bharambe.
Email Id- huteshb AT gmail.com
huteshb AT yahoo.com
_____________________________________________________________________
Carrier Objectives :
To achieve a responsible and challengeable position that will utilized my talent and provides potential for personal as well as organization growth.
Work Experience :
I have experience, at DK Pharmaceuticals Pvt.Ltd.Badlapur as a “Quality Control Chemist” and major responsibilities included Quality Control Analysis of various Chemicals and API Products for a period 18 Months.
Technical skills :
- High Performance Liquid Chromatography
- Gas Chromatography
- UV Sprectophotometer
- Karl-Fischer Auto titrator
- pH Meter
- Melting Point Apparatus
- Brookfield Viscometer
- Nephelometer
- Turbidometer
- Flame Photometer
Research Projects :
A project sponsored by University Grants Commission (UGC)Delhi,
“Eco-friendly Chemical Recycling of Polyamide waste.”

A project sponsored by Moolji Jaitha college,Jalgaon
“Isolation and characterization of milk components using analytical tools.”
Academic Details :
Examination Discipline Board/University Year Class
M.Sc. Analytical Chemistry North Maharashtra University 2011 First Class
B.Sc. Chemistry Mumbai University 2008 Second Class
H.S.C Science Mumbai Board 2004 Second Class
S.S.C. All subjects Mumbai Board 2002 First Class
Computer Literacy :- MS-Office
Article published :
Article name : - “Chemical Recycling of Polyamide Waste”
Published in : - Articles of Research Projects of Budding Researchers
under CPE programme of University Grants Commission
Extra Curricular Activities :
Seminar and poster presentation of “Eco-friendly Chemical Recycling of Polyamide waste” in the National Conference on Natural Resource Management for Sustainable Development (NRMSD-2010)

[Guest]

CURRICULUM VITAE
ANIRUDH KUMAR
Email id : kumarchemgndu AT gmail.com
*OJECTIVES :
Seeking a position to utilize my skills and abilities in a Pharmaceutical organization.

*PERSONAL SKILS :
Comprehensive problem solving abilities, positive attitude, willingness to learn, team facilitator, leadership quality.
*QUALIFICATIONS :
S.No. Levels Passing %age Board/university
1. M.Sc.(Industrial chem.) 2008 60.0% G.N.D.U.Amritsar
2. B.Sc (P.C.M) 2004 60.0% H.P.U.Shimla
3. +2(P.C.M) 2001 54.0% H.P.B.S.E.Dharmshala
4. 10th 1999 68.0% H.P.B.S.E.Dharmshala

*ORGANIZATION : Ranbaxy Lab. Ltd (MNC-All plant FDA approved).
*DESIGNATION : Quality Control Officer.
*EXPERIENCE : 3 years
*JOB ROLE :
1. Analysis of Raw Materials/Intermediates/Finished Goods.
2. Calibrations of instruments/Qualification of instruments.
3. Maintain Inventory of chemicals and chromatography columns.
4. cGMP/GLP compliance in QC laboratory.
5. Documentation as per cGLP.
6. Handle USFDA, TGA, WHO, EU and customers audits.
7. Ensure all instruments complies 21CFR PART 11
8. Create and Review SOP and specification in Document Compliance system.
9. Initiate OOS/OOT/CAPA in CAPA Quality Management System.
10. Knowledge of Vendor Qualification, change control, Sampling of Raw material/ Intermediate/FG/Packaging Materials testing.
11. Ensure 100% training of all QC employees.
*INSTRUMENT HANDLED :
1. High Performance liquid chromatography.
2. Gas Chromatography.
3. High Performance Thin Layer Chromatography.
4. UV visible Spectroscopy.
5. IR Spectroscopy.
6. NIR Spectroscopy..
7. Karl –Fischer Titration.
8. Volumetric Titration.
9. Potentiometer Titration.
*COMPUTER SKILLS :
SAP System, LMS, CAPAQMS, Chemidraw, MS office, Window XP & vista.

[Guest]

CURRICULUM VITAE
MIRZA ZAHANGIR BEIG
E-mail : mirzazahangir.beig AT gmail.com

CAREER OBJECTIVE
To work as a Pharmaceutical Quality Assurance Professional which is innovative, challenging, and rewarding which offers a profound base to enhance my talent , exposure and zeal of learning.
WORK EXPERIENCE
Working with ACME FORMULATION, NALAGARH (H.P.) approved by WHO,ISO And GMP as a Jr.qa officer from JUNE. 2010 till now.(Tablets & Capsules).
Area of interest
IPQA & QA.
JOB RESPONSIBILITY :
(1) Line clearance for different area like dispensing, granulation, compression, coating,
Packing and filling.
(2) Doing online in- process for quality parameter during Manufacturing of various product.
(3) Collection sample(analysis,control and stability). (4) Reviewing of BMR & BPR.
(5) Ensuring the daily log card and Calibration of equipment & instrument are up-to-date.
(6) Handling of process validation.
(7) Handling of change control & deviation.
(8) Swab from different section.
EQUIPMENT EXPOSURE :
(1) Operation and calibration of Electronic Weighing Balance.
(2) Operation and handling of Leak Testing Apparatus.
(3) Operation and calibration of Friability Test Apparatus.
(4) Operation and calibration of Disintegration Test Apparatus.
(5) Operation and handling of Monsanto hardness tester.
EDUCATIONAL
M.Pharma (Pharmaceutics) : From Kanak Manjari Institute of Pharmaceutical Sciences, Rourkela, Orissa, an Institution approved by PCI, AICTE and affiliated to Biju Patnaik University of Technology with CGPA-8.81
B. Pharma : From Kanak Manjari Institute of Pharmaceutical Sciences, Rourkela, Orissa, an Institution approved by PCI, AICTE and affiliated to Biju Patnaik University of Technology with CGPA-7.26
D. Pharma : From Indra Gandhi Institute of Pharmaceutical Sciences, BBSR,Orissa approved by PCI, AICTE and affiliated to OSBP in first year with 1st div.and second year with 1st div.
Intermediate : From Balikuda College,Balikuda, Jagatsingh pur, Orissa, with 3rd div.
Highschool : From Narendranath Bidyapitha,Purnanga, Jagatsingh pur,Orissa with 1nd div

[Guest]

Dear Sir,
This is Jahir Hussain, (Microbiologist)
I have around 16 years hands of experience in PHARMACEUTICAL MICROBIOLOGY
Please consider my attached C.V. for the post of QUALITY CONTROL - MICROBIOLOGIST
Best regards
Jahir Hussain
QC/Microbiology Senior Analyst
CURRICULUM VITAE
Name : M. JAHIR HUSSAIN

email : ayd.jahir AT gmail.com,ayd_jahir AT yahoo.com
Educational Qualifications : Bachelor of Science (B.Sc. – Botany)
: Bachelor of Education (B.Ed. – Biology)
Training Courses :
1.ISO 9002 Quality Awareness Course
2.Good Manufacturing Practice
3.Good Lab Practice
4.Health & Hygiene Training
Member of Pharmaceutical Microbiological Forum(PMF)

Professional Experiences : Worked as a Q.C- Microbiology Technician
Manufacturing Sterile Surgical Devices in
Compliance with Quality Standards
ISO 9000, EN 46000 & CE
United Medical Industries Co. Ltd, Riyadh
(Jan 1997 to Feb 2003)
: Working as a Senior Microbiology Analyst
(QC-Microbiology) in a Leading and US FDA Approved Pharmaceutical Co.
Jazeera Pharmaceutical Industries (JPI), Riyadh, K.S.A
Since June 2003 till date.
Instruments Handle : Autoclave, ETO sterilizers, Milliflex Pump
Laminar flow cabinet, fume cabinet, Microscope,
Incubators, Vacuum dryers, Ultrasonic bath,
Water Bath, Digital thermocouples, pH meter, Thermometer, and Colony Counter.
Responsibilities :
- Microbial Water sampling and testing of De-ionized water, Tap water, raw water.
- Microbial limit test for raw materials, finished products and stability samples such as Syrups, Creams, Ointment, Tablets, Suspension, Flavors, gelatin capsule etc, as per USP, EP & BP methods.
- Environmental monitoring of Air sampling, Surface sampling, Settle plate, Rodec plate method and Finger tab test.
- Suitability test for Raw materials, Antimicrobial Preservative Effectiveness test and test method Validation for Finished product. Sterility test for sterile product.
- Antiseptic-Disinfectant efficacy evaluation by use dilution method for Dettol, 70%Alcohol, Liquid hand Soap.
- Preparation of different types of Culture media, reagents and standardization size of inoculums.
- Prepared culture media test for pH, Growth promotion, Inhibitory, Sterility and Indicative test.
- Calibration of Microbiology Lab pH meters and balances.
- Identification of bacteria and fungi by biochemical methods such as gram staining, Oxidase,
Catalyst, Endospore and API kit. Re-hydration of Bacteria and Fungi from stock culture.
- Control the stock arrangement purchase orders for any shortage in culture media, Bacteria and Fungi from ATCC and Disposable items.

- Investigation for any out of limit results. Labs. Supervising, data collection, entering and
Reporting to manager.

[Guest]

CURRICULUM VITTAE
SK SABER ALI
E mail : saber_bpharm AT yahoo.co.in ,
Objective :-
Looking forward into work in a supportive and co-operative environment with opportunities to enrich my knowledge, experience and skill in the emerging and challenging pharmaceutical field while contributing my best.
Interested in : -Pharma companies in Saudi Arabia and other gulf countries.
Strengths :
- Able to work in flexible schedule
- Zeal to take challenge and keep learning
- Equal effective ,working independently or in a team management
Professional Experience :-
Worked as a technical supervisor (Production-Packing) in Zydus Healthcare (Zydus Cadila), Sikkim (INDIA) from August 2006 to February 2008.
Worked as Senior Executive (Production-Packing) in Dr Reddy’s Laboratories Ltd. Hyderabad, Andhra Pradesh (INDIA) from March 2008 to November 2010.
Working as Executive (Production-Packing) in Ind-Swift Laboratories (GBU), Derabassi, Mohali, Punjab (INDIA) since December 2010 to till date.
Job Profile : Equipments Handled:
Independently Handling , Changeover, operation and Troubleshooting of Blister Packing Machine PG 230XT, Unipac (PAM-PACK),Alu-Alu Pack-BQS (PAM-PACK), EPI-2500 (Elmach), Rotovac 210 (P.G), 240-CH (P.G).
Independently Handling, Changeover, operation and Troubleshooting of Strip packing machine (Sattelite Engineers).
Independently Handling, Changeover, operation and Troubleshooting of Bulk packing machine (Brothers Engineers)

Independently Handling , Changeover, operation and Troubleshooting of Check Weigher Machine(Techno four) and Carton coding printers - Videojet Printer, Condot HSA printer.
Job Responsibility :
- Looking after Tablet & Capsule Packing independently and reporting to Manager Production-Packing.
- Looking afterTablet & Capsule Quarantine independently and reporting to Manager Production-Packing.
- Handling and looking after of all shop floor activities of packing department.
- Maintaining of proper handling and destruction of rubber stereos
- Proper handling and maintaining of Primary & Secondary Packing materials.
- To make and execute daily Production Planning
- Man power handling and target achievements
- To provide shop floor training to subordinate and down the line
- Maintain cGMP Regulatory requirements
- To co-ordinate with service oriented departments such as PPMC, Warehouse, QA,QC ,HR & A and Engineering department for day to day activity
- To maintain and ensuring to keep online of documents and BPRs related to manufacturing & packing.
- Preparation of BPRs and SOPs
- Preparation of monthly Reports related monthly outputs, Overall Equipment Effectiveness (OEE).
Major Achievements :
- Worked with ZYDUS CADILA since project stage.
- Exposure to initial teething problem during initiation of production activity till streamlining of all production activity
- Experience while installation of all sorts of machine and equipments related to production & Packing for 1st time
- Special Exposure for being a part of the project team of Zydus Healthcare.
- Attained 700 minutes cGMP training form CALGS.
- Participated in Safety Training organized by Safety Team, Dr Reddy’s Laboratories Ltd.
- Faced MHRA, USFDA and ANVISA audit.
Educational background :
B.Pharm from NORTH BENGAL University (W.B) in 2006 with 75.18%
D.Pharm from West Bengal State Council of Technical Education in 2003 with 70.8%
Higher secondary school examination from WBCHSE in 2000 with 67.3%
Secondary school certificate from WBBSE in 1998 with 80.04%

[Guest]

CURRICULUM VITAE
Name : - JUNED AKHTAR
Email ID : - Juned.bfit AT gmail.com
Designation- MICROBIOLOGIST
CAREER OBJECTIVE :-
To serve in a dynamic and growth oriented organization where I can utilize my knowledge as well as potential to achieve the organization goals.
PROFESSIONAL QUALIFICATION :-
- M.sc Microbiology from H.N.B Garhwal Central University, 2011
- Bachelor of Science in applied Bio-technology from Sikkim-Manipal University of Health, Medical & Technological Science,2009

ACADEMIC QUALIFICATION :-
- Intermediate with (Science) from, UP Board Allahabad in 2006.
- High School from B.S.E.B, Patna in 2003.
COMPUTER SKILLS :-
- Basic knowledge of computer
- Windows 98/2000/xp
- MS office : Word, Excel, PowerPoint
- Internet
INTERNSHIP-
- Company : IPCA LABROTRIES
Location : Dehradun, Uttrakhand(India)
Duration : 1 Month
Project : QC

- Company : LUMBINI BEVERAGE PVT.LTD
Location : Hajipur Bihar(India)
Duration : 1 Month
Project : Water treatment plant
STRENGTHS :-
- Communication skills, Convincing power
- Integrity, Positive Attitude & Honesty
- Punctuality, Hard worker and loyalty.
TECHNICAL SKILLS
- Microbial Media Preparation and cultivation of microbes using standard microbiological method.
- Growth, isolation techniques (Agar plating method), identification of microorganisms.
- Staining Techniques (Simple Staining, Negative Staining & Gram Staining).
- Microbial Assay of Antibiotics by Diffusion Method.
- Cultivation techniques for isolation and enumeration of microorganisms.
- Microbiological examination of air, water, food, soil and dairy products.
- Clinical screening of various body parts for pathogenic microorganisms.
- Microbial limit test and pathogen test of R.M., Bulk and Finish goods.
- Rehydration, maintenance and identification of stock culture.
- Bioburden tedt.
- Environmental and personnel hygiene monitoring(By settle plate and air sampler, swab test).
- Autoclave validation.
- Water vailation.
- Growth promotion test.
- Preparation of document related to tests.

EXPERIENCE-
- Presently working as a Microbiologist with FMCG Company Sarvotham
Care(manufacturer of AMWAY product) Baddi, H.P. from Sept.2011 to till now.
- Worked with Shahara hospital lucknow, U.P as a Microbiologist from jan 2011 to august 2011.

[Guest]

SATPAL VERMA
Email :satpalverma1982 AT gmail.com

CAREER OBJECTIVES :
To learn current and relevant technology from your vast experience and use it in combination with my acumen and sound knowledge acquired over the years to develop effective skills to maximize individual and organizational productivity
WORK EXPERIENCE :
Total Experience – 6.0 Years
- Rene Industries Limited Kampala Uganda at the designation of Manger Q.C [Nov 2011- present]
- Ranbaxy Lab Ltd, Mohali (Pb.) at the designation of Sr. Officer Q.C. USFDA Approved plant. [Aug 2010- Oct-2011]
- Jubilant Life sciences Noida at the designation of Research Associate in Analytical Research and Development. [Jan 2010. – Aug 2010]
- 3 Years & 3 Months of experience in Torrent pharmaceuticals Ltd, Baddi (H.P) as QC Executive. [ Sept 2006– Dec 2009]
JOB RESPONSIBILITIES :
Current
- Coordinate with other section/department on day to day basis for timely data collection, timely review and release of RM and PM.
- Accountable for Compliance in GLP, RM, PM, FP, Stability & Documentation
- To Review and Approval the Certificate of Analysis/Trend report after completion of review of the raw data of Raw Materials, Packing materials, Finished Products and Stability Products.
- Review the Protocol, Report for Process Validation
- Responsible to investigate OOS/OOT reported in QC department.
- To ensure & review compliance of GLP in the QC Lab.
- To ensure & review calibration & AMC of all QC instruments as per their schedules.
- Review of the SOPs, Specs, STPs & worksheets of RM, PM, SFG, FP.
- To conduct training for QC personnel
At Ranbaxy Lab Ltd :
- Review of analytical data and maintenance of GLP compliance in Laboratory.
- A member of Technology Transfer team and receives new methods from R&D on plant location and transfer analytical method to other plants.
- To solve trouble shooting and analytical related problems.
- Handling of OOS, investigations and Deviations.
- Performing and verifying calibration, qualification, validation & preventive maintenance of instruments and measurement devices as per schedule in Quality control.
- Routine review of SOPs for adequacy and compliance.
- Providing inputs during internal and external audits.
At Jubilant Organosys Ltd :
- Analysis of drug substances using chromatographic technique and providing analytical support to CRD department for development of new molecule.
- Impurities profiling of various projects.
- To solve trouble shooting and analytical related problems
- Review of analytical data and maintenance of GLP compliance in Laboratory.
- Calibration of instruments
In Torrent Pharmaceuticals Ltd :
- Testing of raw materials, in process, intermediate, semi-finished , samples and finished
Pharmaceutical products.
- Preparation of Working Standard and maintaining their records
- Preparation of standard operating procedures, product data sheets, standard test procedure and specification under the guidance of the section head.
- Calibration of HPLC, UV, FTIR, Autotitrator, KF Apparatus.
- Providing Inputs during internal and external audits
- Working in environment, which follows GLP

ACADEMIC QUALIFICATIONS :
M.Sc. (Organic Chemistry) Secured 68.0%
COMPUTER SKILLS :
Operating System : MS-Office.
System Software : Exposure to end usage of SAP
Documentum Compliance Manager (SOP/STP/GP)
CAPA-Track wise Software(OOS,OOT& Deviations
Learning Management System Software( Trainings)
INSTRUMENTS HANDLED :
- HPLC (Dionex, Shimadzu, Waters) (UV-Visible, RI,PDA Detectors)
- UV- Visible Spectrophotometer. (Perkinelmer, Shimazdu)
- Dissolution Test Apparatus, Disintegration Apparatus.
- FTIR( Perkin Elmer Spectrum1 & Spectrum100)
- Autotitrator(Metrohm-836) , Karl Fisher Titrator (Metrohm-841)
AUDITS FACED
- USFDA
- EU GMP
- ANVIZA (Brazil)
- WHO
- NABL
- NDA (Uganda)

PERSONAL DETAILS :
Date of Birth : 2nd Feb 1982
Nationality : Indian
Gender : Male
Marital Status : Single
Language Known : Hindi, English
SATPAL VERMA

[Unregistered]

Personal information
First name(s) / Surname(s) Gohar Ali
Rawalpindi. (Pakistan)
Nationality Pakistani
Date of birth 20/09/1976
Gender Male

Desired employment / Occupational field : Quality Control, Pharmaceuticals Industry

Work experience :
Dates 11/12/2007
Occupation or position held :
Sr. Assistant Manager Quality Control :
Main activities and responsibilities :
- Preparation of finished product dossiers for the registration in different countries for export purposes.
- Tested many new drug products for their stability Ongoing and accelerated conditions and determination of the shelf life of various products.
- Control of the quality of drug products during production to ensure that they meet standards of potency, purity, uniformity, stability and safety.
- On the basis of research work have developed the new analytical Methods for the analysis of products including solid dosage form and Pharma Injectables products. Delivered excellent results as far as cost effectiveness of the production is concerned.
- The Stability studies of new products and existing products i.e. accelerated stability and on going stability and its monthly stability schedule, On the basis of the stability studies we fixed the expiry dates of many products.
- Particularly the Validation of Analytical Methods, Process validation and after wards its successful and uninterrupted operation as per cGMP standards.
- Have performed the analysis of Infusion, Injectable, Solid dosage Form and Liquid Dosage Dry suspension etc. by using UV Spectrophotometer, titration and HPLC.
- To collect the sample of incoming raw materials, in process and finished. Performed the required testing to ensure the proper disposal of chemicals and maintain the record of the disposal.
- Involved in the analytical testing of raw materials, finished products. Worked on FTIR, HPLC, and UV Spectrophotometer.
- Have performed calibration of instruments like HPLC, Moisture analyzer, Balances, Karl Fisher, Disintegration Time Apparatus etc and preparing monthly calibration schedule.
- Compilation of the Validation data and development of various validation protocols for calibration certificates, stability studies Bin cards and their Record keeping is under my control.
- Involved to implement the compliance of all the activities in the Quality Control Department as per WHO guidelines, all applicable regulatory and international standards requirements (ISO 9001 :2008).
- To implement the compliance of all the internal polices approved by managing Director.
- To adopt the cost effective measures to enhance the overall profitability of the organization and strive continuously for the improvement of skills.
- Well knowledge and well aware about Microbiological Tests and Clean Rooms.
- Also performed Sterility Test of Sterile Products (Dry Powder & Liquid), performed LAL Test (Chromogenic & Gel Clot Methods) of Sterile Raw Materials, Intermediates, and Finished Products as well as Water.
- To monitor clean rooms by using Particle Counter for Non-Viable Particles and also Biological Air Sampler for Viable Particles.
- Also can operate Colony Counter, Microscope, Validation of Dry Heat Sterilizer and Steam Sterilizer.
- Media Preparation, performed Growth Promotion Test of Media, Zone of Inhibition Test (Bio-Assay of Antibiotics).
Name and address of employer Global Pharmaceuticals Islamabad,
Plot # 204-205, Industrial triangle Kahuta Road, 46000 Islamabad (Pakistan)
Type of business or sector : Pharmaceuticals Manufacturing

Dates 2004 - 2007 :
Occupation or position held : Senior Quality Control Analyst
Main activities and responsibilities :
- To analyze Semi finish/ Finished products and raw materials by using HPLC, UV-Visible Spectrophotometer and titration method and to maintain their records.
- To look after the stability testing for products on specified conditions and to maintain their records.
- Sampling of raw materials and analysis of packaging materials and to maintain their records.
- Preparation of volumetric and test solutions.
- Calibration of laboratory instruments.
- Have performed the analysis of Solid, Liquid and Injectable dosage form by using HPLC, UV Spectrophotometer.
- Directly involved in the Process (prospective) validation of newly launched products, analytical method validation, concurrent validation, cleaning validation.
- Compilation of the Validation data and development of various validation protocols for calibration certificates, and their Record keeping is under my control.
- The Stability studies of new products and existing products i.e. accelerated stability and on going stability and its monthly stability schedule, On the basis of the stability studies we fixed the expiry dates of many products.
- To collect the sample of incoming raw materials, in process and finished. Performed the required testing to ensure the proper disposal of chemicals and maintain the record of the disposal.
- Involved in the analytical testing of raw materials, finished products. Worked on HPLC, UV Spectrophotometer.
- Involved, to implement the compliance of all the activities in the Quality Control Department.
Name and address of employer Vision Pharmaceuticals
Plot # 224, I-10/3, Industrial Area, 46000 Islamabad (Pakistan)
Type of business or sector Pharmaceuticals Manufacturing

Dates 2001 - 2002 :
Occupation or position held : Quality Control Analyst
Main activities and responsibilities :
- Have performed the analysis of Solid, Liquid dosage form by using, UV Spectrophotometer and Titration Method,
- Evaluation of labelling, packaging and advertising of drug products,
- To collect the sample of incoming raw materials, in process and finished. Performed the required testing,
- Involved in the analytical testing of raw materials, finished products. Worked on UV Spectrophotometer,
- Tested many new drug products for their stability on ambient and accelerated conditions and determination of the shelf life and Quality as per international standards of various products,
- Have developed new analytical methods for the analysis of new drug products. Involved to implement the compliance of all the activities in the Quality Control Department as per Standard Guidelines, all applicable regulatory and l standards requirements (ISO 9001 :2000).
Name and address of employer Nafar Pharmaceuticals,
Hayatabad Industrial Estate, Peshawar (Pakistan)
Type of business or sector Pharmaceuticals Manufacturing

Education and training :
Dates 1999 - 2001
Title of qualification awarded : Master of Science
Principal subjects / occupational skills covered :Organic Chemistry, Physical Chemistry,
In-organic Chemistry, Biochemistry.
Name and type of organisation providing education and training : University of Peshawar (Govt; Postgraduate College,)
Kohat (Pakistan)
Dates : 1996 - 1998

Title of qualification awarded : Bachelor of Science
Principal subjects / occupational skills covered : Chemistry, Geography, Zoology
Name and type of organisation providing education and training : University of Peshawar (Govt; Postgraduate College,)
Kohat (Pakistan)

Dates : 1993 - 1995
Title of qualification awarded : Inter of Science
Principal subjects / occupational skills covered : Physics Chemistry, Biology, English.
Name and type of organisation providing education and training : Board Of Intermediate and Secondary Education Peshawar (Govt; Degree College, Lundkhwar)
Mardan, (Pakistan)

Dates : 1991 - 1993
Title of qualification awarded : Secondary School Certificate
Principal subjects / occupational skills covered Physics, Math, Chemistry, Biology, English.
Name and type of organisation providing education and training : Board Of Intermediate and Secondary Education Peshawar (Govt; High School, Lundkhwar)
Mardan, (Pakistan)

Personal skills and competences :
Mother tongue(s) Pashto
Other language(s) :

Social skills and competences : I am young, confident, hardworking and reliable person with full professional commitment. I compose a friendly disposition with a good sense of humour. I can work well under pressure, either as an individual or a part of a team. Combined with my dedication, determination and hard work, the same shall help me go up the specialist ladder.

Organisational skills and competences : Self initiator, devotion and dedication to work, work in a challengeable atmosphere, proven administrative ability, communicate effectively with people from other cultures, cheerful under pressure, remain enthusiastic ever in the face of frustration, persistence, personal contact, self reliance and confidence are those factors which have helped me to maintain a consistent record of achievements.

Technical skills and competences : Good command of quality control processes (I was responsible for the implementation of quality audit in my deptt.).

Computer skills and competences : 1. Computer awareness
2. MS Office, Internet and E-mail etc.

Other skills and competences : 1. Training Course: “Two days training on Stability Testing/cGMP Compliance held on January 10-11, 2007 by Pakistan Pharmaceutical Educational Foundation.
2. Training Course : Process Development & Validation 11th march 2006 held by Ministry of health.

Driving licence(s) A, B

[KAILASHPANT]

Looking for a Challenging Job in Quality Control Department as Executive / Technician (analysis & Instrumentation)

[Unregistered]

Sir, i am Lahu Pathare, i am M.Sc. Organic chemistry passout at june 2010 with first class. i have 3 years experiance in organic synthesis in cipla pharmaceauticals.

[Unregistered]

KESKAR NAGNATH BALKRUSHNA
E-mail : keskar2011 AT hotmail.com / nagnath72 AT rediffmail.com

Professional Summery :
** Professional experience of 15 years in Pharmaceutical Industry As Analyst (Q.C.) / Senior Analyst/ Q.C. In charge with different organizations

Working with UMANG PHARMATECH PVT.LTD Vasai as a Q.C Head from 20 March 2010 to till date.

** Worked with JASMIKA HEALTH CARE PVT LTD VASAI AS A Q.C. In charge from April 2009 to March 2010

** Worked with UNIBIOS LOBORETORIES LTD as Q.C. In charge Duration- From Aug 2006 to March 2009

** Worked with LIBERAL PHARMACEUTICAL at Palghar as Q.C. In charge. Duration - Dec 2003 to July. 2006

** Worked with RICHIE LABORETORY LTD. at Vasai as Chemist Duration - Nov.1999 to May. 2003

** Worked with M.J.LABORETORIES as Trainee Chemist Duration - Dec.1997 to Oct. 1999

Educational Qualification :
** B.Sc.(Chemistry) passed with second class from Pune university April 1997
** M.Sc. (Chemistry) passed with First class From Vinayaka Mission University Tamilnadu May 2012

Technical Qualification :
** Having FDA approval in Chemical & Instrument department From FDA Thane (Maharashtra)
** Having FDA approval in Microbiology department from FDA (Thane) (Maharashtra)
** Certificate course in Computer (M.S.C.IT)

Skill summery :
** Analyst Q.C. :
** Handling Spectrophotometer U.V. Visible model Jasco V 530,
** Shimadzu 1201,1701 ,1700 Elico SL-159 , UV Visible
** Spectrophotometer SYS 118
** FTIR ( PerkinElmer, Jasco-410, Nikolite 380)
** HPLC : Model : Jasco,UV 975,PU980 Water 486 ,510( Win Chrome )
** Agilent 1120Compact LC,( Ezichrome Elite Software) Auto sampler
** Shimadzu LC-2010( LC Solution Soft ware )
** GLC : Perkin Elimer With FID ( Iris 32 )
** Karl fisher (Vego,Lab India )Flame photo meter, Dissolution
** Apparatus(Vego, Lab India Disso 2000),Florimeter
** Potentiometer,(Vego),pH meter& other laboratory instrument

Audit Handled :
** WHO Audit Role as a Q.C. Head total responsibility of Quality Control in Jan 2010 In Ms Jasmika HealthCare Pvt Ltd Vasai & Jan 2009 in Ms Unibios Lab Ltd Palghar
** NAFDAC Audit ( Nigeria ) Role as a Q.C.Incharge In Feb 2010 in Jasmika Health Care Pvt Ltd Vasai.
** NDA Audit ( Uganda ) Role as a Q.C .Manager In Feb 2009 in Ms Unibios Lab Ltd Palghar
** ISO 22000 { HACCP } Role as a Q.C. Head Audit in March 2011 in Umang Pharmatech Pvt Ltd Vasai
** Iran Daru Pharmaceuticals ( Iran ) audit Q.C. Head Audit in March 2013 in Umang Pharmatech Pvt Ltd Vasai
** Themes Medicare / Merck audit Q.C. Head Audit in March 2013 in Umang Pharmatech Pvt Ltd Vasai

Professional training :
** Training on Lab Quality system Accreditation as per ISO 22000 at Mumbai.
** Training on Handling & development of Analytical method on different Instrument at Mumbai
** Training on Computer System Validation CFR 21 Part II by IBC Mumbai

Job Description :
** Present Employer :
Organization : UMANG PHARMATEC PVT.LTD VASAI
Umang Pharmatech Pvt Ltd is GMP approved unit manufacturer of Pharmaceuticals,Nutra and cosmetic pellets,extrude& Mouth dissolving Film For domestic as well as export purpose.
Designation : Q.C.Head
Duration : From 20 March 2010 to till date
Responsibilites :
1. Handling about 10 – 15 analytical team and coordinating with about 4 member Analytical QA
2. Monitor analytical activities and experiments in support of the development, including method development, method validation, method transfer, compatibility studies and stability tests as per ICH, MHRA, USFDA, etc…guidelines.
3. Responsible for timely deliverables of laboratory activities related to Chemical, Instrumentation and microbiology testing
4. Provide oversight on environmental monitoring and microbiology during facility validation activities.
5. Ensure laboratory compliance.
6. Ensure regulatory and customer inspections readiness; represent area and participate in audits.
07. Ensure compliant and timely testing of samples received at laboratory and stability samples.
08. Ensure Stability studies and reports are compliant and timely.
09. Evaluate analytical raw data and laboratory analysis.
10. Ensure quality control department and equipment is maintained and reliable.
11. Ensure necessary equipment qualification and validations are complete.
12. Ensure the necessary training within the department is carried out and modified according to need.
13. Monitor and control method performance.
14. Designate and monitor the storage conditions for materials and products.
15. Maintaining Laboratory in compliance with the requirement of cGMP & cGLP and WHO.
16. Preparation and Review of SOP, STP, GTP, Specifications, protocols, etc.
17. To ensure that organization policies and disciplines are implemented and maintained effectively.
18. To notify the management in case of OOS, OOT, Deviation, Change control and to fill the required documents.
19. Timely Investigation and closure of all such notifications with CAPA.
20 To update the system as and when required due to any change, revision in regulatory guideline, pharmacopeias, or any additional customer requirement.
21. Define roles, responsibilities, project scope, timelines and deliverables. Track progress of projects within agreed timelines.
22. Directs Work Instructions to analysts for the testing and analysis of Stability Develop and administer schedules, assign responsibilities within the group Document all laboratory work to meet regulatory standards and perform data Review.
23. Stability testing : Protocol design, Long - term stability test, Drug substance stability testing, Comparator stability testing, Formulation evaluation stability testing, data trending, Forced degradation studies, Photo stability, Temperature cycling.
24. Collect, analyze and interpret data, keep records of experiments including results and conclusions, recognize aberrant results and data trends, and provide plausible explanations including plans for follow up experiments to clarify findings.
25. Assign and perform training and development goals to the group.
26. Achieved deliverables and contributed to meet targets for each quarter.
27. Successfully initiated and executed stability studies with detail trending and investigation.
28. Designed experiments and delivered results, demonstrating awareness of customer demands and focus.
Reporting : Reports to COO

Past employers :
ORGANIZATION : JASMIKA HEALTH CARE PVT. LTD VASAI
WHO GMP approved pharmaceuticals formulation unit. Manufactured general tablets & capsules for export purpose
Duration : From April 2009 to march 2010
Designation : Q.C. In charge
Responsibilities :
** Responsible for total Q.C. department as a Head for third party as well as FDA & other regulatory audits
** Total responsibility of maintain documents, analysis& daily activity in Q.C. Department
** Distribution of work in chemist of chemical, instruments & microbiological
** Department.
** Responding to the Technical Queries of Chemists
** Preparation of Standard operating procedures
** Report cheking and sinning as authorized person
** Responding to the technical quires of the customers
** Responding to the Technical Queries of clients .

ORGANIZATION : MS UNIBIOS LABORATORIES LTD PALGHAR
Duration : From August 2006 to march 2009
WHO GMP approved pharmaceuticals formulation unit. Manufactured general & betalactum tablets & capsules for export and domestic purpose
Designation : Q.C.In charge
** Responsible for total Q.C. department as a Head for third party as well as FDA & other regulatory audits
** Total responsibility of maintain documents, analysis& daily activity in Q.C. Department
** Distribution of work in chemist of chemical, instruments & microbiological

** Department.
** Responding to the Technical Queries of Chemists
** Preparation of Standard operating procedures
** Report checking and sinning as authorized person
** Responding to the technical quires of the customers
** Responding to the Technical Queries of clients.

Organization : Liberal pharmaceuticals at palghar
Manufacture of Tablets, Capsules Liquid oral & ointment for export & domestic purpose
Designation : Quality control in charge
Period : June 2003 to July. 2006
Responsibilities :
** Job allocation of chemists
** Checking Analytical reports, B.M.R., Packing material etc.
** Supervision of different I P Q C work
** Proper supervision in Production & Q.C. department

Organization : Richie Lab Ltd . (vasai)
Designation : Junior Chemist
Duration : Nov.1999 to May. 2003
Richie Laboratory was WHO approved formulation company they have three sections
Tablets, Capsules , Liquid oral They manufacture for Govt supply
** Responsibilities : Sampling of raw material as per SOP 100 % sampling for API and for expients use Square root n+1 formula
** Analyzing raw materials , finished products , as per procedure
** Keeping stability , validation records Working in Microbiology department caring out sub culturing , microbiological Assay of Antibiotics, Idn of E-coli, salmonella in DM
** water and other Compound Making record of plate count, sub culturing, media preparation, swab test, Incubator, etc.
** Working on HPLC , IR , GLC

Organization : M.J. Laboratories ,Wada
Designation : Trainee Chemist
Duration : Dec.1997 to Oct. 1999
M.J. Laboratories was FDA approved public testing Laboratory. They can carry out Different type of pharmaceutical , cosmetic testing
Responsibilities :
** Preparation of volumetric solutions and general reagents
** Analyzing Raw material , finished products ,vitamins ,
** Working in instruments department under supervision of expertise.
** Handling HPLC,GLC , U.V. , IR .

Personal information :
Name : Mr. Keskar N. B.
Date of Birth : 5/6/1972
Marital status : Married
Lang wages Known : Marathi , English ,Hindi
Hobby : Reading & Playing

Declaration :
I here by declare that all the statement furnished here are true to the best of my knowledge
Date :
Place :
N.B.Keskar.