Syed Muhammad A Alam

Syed Muhammad A Alam

$8/hr
Seeking a responsible position as DATA ENTRY JOB OR ANY AVAILABLE RESPONSIBLE POSITIONS; KHI – PK,
Reply rate:
50.0%
Availability:
Part-time (20 hrs/wk)
Location:
Karachi, Sindh, Pakistan
Experience:
25 years
 House # B – 406, Sector – 11 – A, North Karachi, Karachi – 75850; PK: Voice:- OBJECTIVE Seeking a responsible position as Data Entry Job or Any Available Responsible Positions; Karachi (Sindh) – PK, this would value my diverse trade ability to effectively interact and communicate with people, explores solution for difficult problems and work in a positive team-oriented environment CARRER PROFILE * M. Sc. Organic Chemistry (Pharmaceutical Chemistry as an Optional Subject) With Over 25 + Years of Professional Experience in Research And Development; QA / QC / Production / Sales & Marketing Departments of Various Reputed Pharmaceutical; Food & Petroleum / Oil & Gas Services Provided Companies; And Transformer Oil Testing Laboratories Plus Construction Laboratory * Taking The Responsibilities of Providing The Full Support to Managing The Daily Operations of Indus Pharma Divisions. I’ll Be The In-Charge of The Analytical Method Developments, Product Characterizations, to Provide The Supports For Process Design / Characterization And Also Support to Company’s Regulatory Related Filings; Which Are Includes Structural And Degradation Pathway And as Well as Resolving The Stability Issues And Support to The Formulation Development * Having Strong Knowledge of cGMP’s, GLP’s And GDP’s; According to FDA, HPFBI “Health Products And Food Branch Inspectorate (Canada)” And ICH Guideline Rules All The Times And Also Operation, Calibration And Trouble Shooting of All Modern Analytical Equipment’s, e.g. HPLC, GC, FTIR & Assurance GDS / PCR / DNA & UV-Vis Spectrophotometer, And TLC Techniques, Karl Fisher, Dissolution & Disintegration Apparatus & Also Development of New Analytical Testing Methods On HPLC Techniques With The Exposure of LIMS (Laboratory Information Management System) * Computer Skills By Using Software Such as MS Excel, MS Word, Outlook, a Document Management System; With Specialized By Using Scientific & Analytical Software Such as WinLIMSLink Method / AIM; WinELN Form / Labtronics to Enter, Manipulate And Report Data Performing ATM Validation, Equipment And Manufacturing Processes & Writing SOP’s Test Methods & Specs. * Routine Stability, Accelerated Stability And Post Marketing Surveillance Studies With Having New And Existing Products. * Verify The In-Process / Final Results & QA; Support Annual Product Review (APR); Trend Charting of Critical Process Parameters And Analytical Results, Identification of Corrective & Preventive Actions (CAPA) * Performing All Day-To-Day QC / QA Activities of Routine Tests And Release For Production * Self-Inspection And Internal cGMP Audits, Compliance Audits & Vendor Audits * Highly Motivated, Energetic, Confident, Highly Self-Driven, Independent And Having Excellent Interpersonal And Presentation Skills, Works Effectively in Multitask Environment With Cross-Functional Teamwork Activities By Taking Pride With The Doing Job EMPLOYMENT HISTORY The National Absorbent Cotton Mills Co.; (Karachi) Manager Quality Assurance (Resign) Dec 2020 – Dec 2020 * The Prime Function As “Manager Quality Assurance” is to Coordinates All Activities Involving Development, Implementation, And Maintenance of Quality Management Systems And Compliance Across The Company * As “Manager Quality Assurance” is Responsible For The Variety of Quality Standards And Whole Processes, Including ISO Standards, IQ (Installation Qualification) / OQ (Operational Qualification) / PQ (Performance Qualification) Validation, And PPAP (Production Part Approval Process) Executions at The National Absorbent Cotton Mills Co. * Also Develop, Manage And Maintain The Company’s Quality Programs And Secure Resources to Support The Project On Time Delivery * Serve as Administrator / Management Representative of Companies Quality System And Also Ensure That ISO Compliant Documents Are Created And Maintained * Coordinate And Conduct Quality Audits, Document Results, Implement Corrective Action to Ensure The Controls Are in Place Such That All Manufactured Products Conform to Company And Client Defined Quality Standards And Also Ensure Documentation And Maintenance of Corrective / Preventative Action Plans, Customer Complaints, And Vendor Complaints Including The Coordination of Follow Up to Ensure Timely Resolution of Complaints * Manage And Perform Client Requested First Article Inspections; And Also Responsible For Maintaining And Updating The Quality Manual And Communicating Updates Within The Organization * Responsible to Developing And Executing Client Specific QA Plans That May Include PPAP And IQ / OQ / PQ Validation To Ensure The Production Area Has Appropriate Equipment / Technology to Perform Needed Measurements And Inspections. Indus Pharma (Pvt.) Ltd.; (Karachi) Lead Analytical Method Development (Resign) Apr 2019 – July 31, 2020 * The Main Functions as “Lead Analytical Method Development” is a Senior Management Positions And Are The Prime Responsibilities of Providing The Leadership Quality And Managing The Daily Operations of The Method Development And Process Development in The Indus Pharma Divisions * Develop New Products By Using Formulation Skills And Technologies Based On Relevant Consumer Insights in Support of Brand Initiatives. Agree And Secure Resources to Support The Project On Time Delivery * Having Full Command And Experience in Analytical / Process Development With Hands-On And In-Depth Understanding of Different Drug Products Characterization Techniques And Associated Instrumentation Such as HPLC / UPLC, Capillary Electrophoresis, GC, LS / MS etc. * Collaborate With Marketing to Develop, Prioritize And Execute Project Portfolio * Work Cross-Functionally And The Lead Project Teams to Achieve Key Milestones And Their Objectives *As “Lead Analytical Method Developments” With Having Full Responsibilities to Ensure Timely Development of New Formulations For Indus Pharma Divisions of Ongoing / Pipelines Activities of Product Development Programs; & Transfer of Analytical Methods to In-Process And / or Drug Substance (DS) / Drug Product (DP) Release Supports * Plan And Execute Necessary Characterization; These Include Structural And Degradation Pathway Characterizations as Well; With Resolving Stability Issues And to Support The Formulation Development * Lead And Advance Multiple Projects Through The Product Development Process Within The Team * Interface With Key Partners And Stakeholders; (Supply Chain, Production, QA / QC Team, Regulatory Affairs & Marketing) * Lead The Development of Technical Product Strategies to Support Product Development With Short-Term And as Well as Long-Term Innovation * Evaluate And Implement The New Analytical Method Development Technologies; Collaborate And Coordinate With Other Colleagues From Basic Research, Involving And Taking Initiative During The Product Development, Process Development, Manufacturing Process, QA And QC Teams And Also Providing The Full Support And Guidelines of How to Increase The Product Quality * Coordinate The Product Development, Process Development, Manufacturing Process, QA And QC Teams With Pharmaceutical Chemistry For The Test Method Development And Performing of QC For The Stability Studies of New Products Pharmatec Pakistan (Pvt.) Limited.; (Karachi) Assistant Manager Quality Control (Resign) Mar 2017 – Jan 07, 2019 * The Key Functions as “Assistant Manager Quality Control” Were to Assure And Provide Assistance to The QC Manager in Administration Matters of The Quality Control Department And Officiate in His Place During The Absence From Quality Control Manager. * Provide Assistance to The QC Manager in Efficient And Systemic Organizations And Working of Packaging Section Including Physical Inspection of In-Process Bulk And Finished Products, Stability Samples or as Per Work Plan * Recommended to The QC Manager Means of Improving Efficiently And Reducing Cost in The Department Consistent With Company’s Standard * Prepare And Revise Specifications And Test Methods of Packaging Component And Provide The Necessary Required Training of All The Staff of Packaging Section. * To Ensure Good Laboratory Practices And Lab Safety Rules Are Strictly Followed And Implemented of All The Staff in The Packaging Laboratory * To Ensure Calibrations And Regular Service of All The Equipment’s of The Packaging Section According to Their Relevant SOP’s * Provide Support in Updating of Packaging Materials / Monographs And Finished Products Specifications And Test Methods According to BP / USP * To Ensure That Logbooks, Registers, Trend Cards Are Systematically Arranged, Accessible, Properly Filled, Signed And Correctly Kept in The Designated Area * To Ensure All Observation / Findings Identified in Self Inspection And Internal / External Audits Are Properly Addressed And Closed Out as Per Given Timelines * Provide Duly And Timely Support in The Analysis And Documentation of Export Products / Local Regulatory Documentation * For Making Daily Work Plan With Assign to All Analyst And Sign The Report After The Status Will Be Done * To Ensure Good Human Relationship Within The Section And Other Departments And Established Two – Way Communications Down to The Lowest Level to The Staff Pharmatec Pakistan (Pvt.) Limited.; (Karachi) Senior Quality Control Officer (Promoted) Sep 2016 – Mar 2017 * The Primary Responsibility as “Senior Quality Control Officer”; (Packaging Laboratory) Were to Assured That The Quality of The Product Throughout Facility, Through Supervising & Work Assigning of All The Senior Quality Control Officer / Quality Control Officer For The Performing of Physical Testing / Microbiological Testing of Packaging Materials Dimension / Physical Inspection of The Product By Using Balance, Micrometers / Vernier Caliper, Screw Gauge Plus Artworks And Development of New Products * To Ensure Laboratory’s Packaging Components And Equipment’s Accessories Are Readily Available * Also Performing of Some Basic Chemical Testing (e.g. Glass Bottle Alkalinity Test), & Sample Formulations, Disintegration Test, Friability Test, Hardness Test, Aluminum Foil For Lacquer Test, PVC / PVDC For Performing of Identification Test By Using Instrument FTIR, Vacuum Drying Oven For Loss On Drying (LOD) For Empty Gelatin Capsules. Variperm Canada Limited.; (Calgary) Pipe Drilling Associate (Lay Off) Nov 2013 – Mar 18, 2015 * The Main Functions as “Pipe Drilling Associate” Were to Assure That The Quality of Product Throughout The Facility & Working Alone or Together in The Manufacturing Process of The Product With Wearing PPE’s & Follow-Up The OHSE Rules & Regulations All The Times * As “Pipe Drilling Associate”; Supervise & Work Assigns to All The Drilling Bay Staff & Responsible For; To Make Sure That All The Required Services Followed By Variperm Specs & Also Verified / Completed Job Order Documentation as Per Client Job Product Specifications * The Perforation Zones Are Carefully Measured & “Marked Out” Before The Perforation Process Will Begins. Although The Standard Variperm Perforation Patterns Are Used For All API Casing And Tubing Sizes; There Will Be Many Instances When Customer Specified Hole Patterns Are Required & Then After That Going Through The Spring Loaded De–Burring Tools / Hole Horns, De–Burring, High Pressure Air Jets & Drifting etc. * Technically Sound And Understand The Floor Line Area & Are Also Fully Involved in Different Parts of The Machinery Together or Performing Them as Per Our Variperm Specs. * Well Performing Repetitive Duties as Per Assign By Our Manufacturing Manager or as Per Defined By Variperm Job Order Specs. Weidmann Diagnostic Solutions Ltd.; (Calgary) Associate Chemist (Lay Off) Sep 2011 – Jan 27, 2012 * Organized, Analyzed And Performed The Insulating Oil Testing By Using Latest Instruments Like; Dissolved Gas Analysis (DGA), FTIR And Karl Fisher, IFT * Supervise & Work Assigns to All Lab Techs & Sample Prep Techs; Prepare Solutions, Reagents & Sample Formulations * Analyzing Insulating Testing of Acid / Neutralization Number ASTM–D974; Moisture / Water Content ASTM–D1533B; Dielectric Breakdown Strength 2.54 mm Gap ASTM–D877 & 1.0 mm Gap ASTM–D1816 –1.0 & 2.0 mm Gap ASTM–D1816–2; Oxidation Inhibitor Content ASTM–D2668; Power Factor @ 250C; & @ 1000C; ASTM–D924, Interfacial Tension (IFT) ASTM–D971, Specific Gravity By Using Digital Density Meter # DMA–35; ASTM–D1298, Color / Visual Examination of Oil ASTM–D1500 / ASTM– D1524; Viscosity Test By Using Viscometer ASTM–D445–10 ASTM (American Society For Testing & Materials) * Performing Calibration & Validation of Analytical Testing Methods, Equipment According to Weidmann’s Written SOP’s & ASTM Defined Procedure & Compile Records in WinLIMSLink Method / AIM; WinELN Form / Labtronics & Interpret The Experimental or Analytical Results & Deviation Management, Deviation Categorization And Associated Remedial; CAPA’s MFS Canada Food Safety LLC. (High River) Laboratory Analyst (Resign) Dec 2010 – Sep 2011 * The Prime Responsibility as Laboratory Analyst is to Test And Analyzed The E. coliO157: H7 By Using The Latest Laboratory Instrument Like Assurance Genetic Detection System (GDS) as Per Defined By US Bio Control Dept. & Maintain The Records of All Quality Control / Quality Assurance Activities As Documented in Procedures And Test Methods * Work Assigns to The Junior Analysts / Technician Staff; & Maintain The Temp. / Pres. Control Log Books, Prepare Solution, Reagents & Sample Formulations * Verify In-Process / Final Results & QA; Compile Records in Qualink / Qualtrax & Interpret Experimental or Analytical Results * Assist in Developing And Conducting Sampling And Analysis as Per Written Analytical Testing Procedure’s (ATP’s) Hunting Energy Services (Canada) Ltd.; (Calgary) Quality Assurance Auditor (Lay Off) Nov 2008 – Aug 2009 * The Primary Functions as “Quality Assurance Auditor” Were to Assure That The Quality of Product Throughout The Facility, Through Auditing or Physically Gauging / Dimensions / Inspection of The Product By Using Micrometers, Optical Comparator / Shadowgraph And Bore Gauges. * Verified First Off / Last Article Includes Molds / Traces And Completed Documentation For Product Dimension * Verified The Metrology Casing Materials of Catalyst & Base By The Ratio of 50:50 %; For Making Molds to Verify The Threads, Seal Length, Radius / Angle, Groove Depth, Counter Bore Depth of Pipes & Couplings as Per API / Overlay Drawing / Hunting Specs. * Well Versed to Use The Comparator Instrument of First / Last Articles, In-Process Inspection / New-Chaser / Tools / Inserts or as Per Defined By Hunting Specs. * Performed Zinc-Copper Phosphate Inspection Procedure (CrysCoat OC) of Pipes And Couplings Threads By Using Titration Method And Also Check The Content of Total Acid, Free Acid And Iron Content * Validated Mill Certificate & Their Chemical Composition of Raw Stock / Billet Materials & Also Verified Final Inspection of The Product. Petro-Canada Ltd.; (Toronto) Assistant Manager (Lay Off) Apr 2004 – Feb 2008 * Performed General Administrative Duties And Provide Leadership in The Area of Customer Service * Maintained Above And Beyond Care And Attention All The Times For All Customers * Coordinated in All Phases of Work Done By Colleagues And Work as Team * Determined Customers’ Need And Had Keen to Awareness of Product Knowledge And in Store Merchandising * Controlled Day-To-Day Operations of The Store And Monitored The Operation of The Counter * Provide Assistance in Training of Sales And Supervisory Staff’s Other Duties as Assigned By Manager Petro-Canada Ltd.; (Toronto) Customer Service Representative (Lay Off) Nov 2003 – Apr 2004 Spencer Pharma (Pvt.) Ltd.; (Formerly Fison’s Plc. UK); (Karachi) Senior Chemist (Resign) Jun 1998 – Oct 2003 * Organized, Analyzed And Performed The Chemical Testing of Finished / Bulk Products By Using Latest Instrument Like HPLC, UV-Vis Spectrophotometer, FTIR, TLC Techniques, GC, Karl Fisher Auto Titrator And Dissolution Apparatus * Analyzed Raw Materials of Samples as Per SOP’s / USP / BP / EP / JP or as Per Defined By Spencer Pharma’s Specs. * Performed Stability Testing of All Products at Various Temperature / Humidity Conditions Investigated And Generated The LIR Upon Out of Specifications (OOS’s) Results * Also Provide Technical Solution For Drug Analysis And Performed In-House Preventative Maintenance of Laboratory Equipment * Implement The Rule of cGMP / GLP as Per Corporate And Regulatory Standard & Working Experience of Analytical Method Development And Validation. Ankaz Pharmex (Pvt.) Ltd.; (Karachi) Quality Control Manager (Resign) Sep 2001 – Oct 2003 * Monitored And Checked All Types of Pharmaceutical Active And Non-Active Ingredients According to USP / BP / EP * Provided Technical Solution For Drug Analysis And Performed In-House Preventative Maintenance of Laboratory Equipment * Reviewed of Stability Reports, Monograph According to BP / USP And Updated The QA Related SOP’s * Created And Complied SOP’s Training Manual For Junior Staff And Also Arrange In-House Monthly Training of QC / QA / Production / Inventory Control Staff Pfizer Pakistan Ltd.; (Formerly Park – e – Davis & Company (Pvt.) Ltd.); (Karachi) Management Trainee Officer (Resign) Sep 1997 – Mar 1998 Getz Pharma (Formerly Saitex Pharma (Pvt.) Ltd.); (Karachi) Sales Promotion Officer (Resign) May 1994 – Nov 1994 IBI Pharmaceutical Promotion Bureau; (Karachi) Sales Promotion Officer (Resign) Jan 1993 – May 1994 SECA Italy Pakistan Limited.; (Karachi) Laboratory Technician (Resign) Jan 1992 – Dec 1992 EDUCATION AND PROFESSIONAL / COURSES * M. Sc. in (Organic Chemistry) With “Pharmaceutical Chemistry” as An Optional Subjects From University of Karachi, in 1997 * Obtained Academic Educational Credentials From University of Toronto, in 2005 * Completed Research Project Work On “Organic Syntheses” For The Studies of The Chemical Reaction of Mangeiferin, in 1996 * B. Sc. (Major With Chemistry / Microbiology / Zoology) From The University of Karachi; in 1991 * Accreditation as a “Professional Chemist (P. Chem.); # M – 0532 From ACPA at Alberta – Canada; in 2012 * Completed USP Education And Achieving Certificate of The Foundations of GMP – API; Through Online at Karachi, Sind – Pakistan; in 2020 * Completed Twenty Days Certificate Training Program in Fiqah And Hades Learning Course Which Are Organized By Siddiq– e –Akbar Mosque Under The Supervision of Mufti Mr. Obaid-Ullah at Karachi, Sind – Pakistan; in 2019 * Getting On Job Training Orientations From Production / Dispensing / Quality Assurance / Quality Control / Regulatory Affairs / Research & Development And Product Development / Warehouse / Supply Chain Management / Engineering / Human Resources & Administration / HSE, PPE & MSDS From Pharmatec; Indus Pharma at Karachi, Sind – Pakistan * Completed Eight Weeks Advance Good Manufacturing Practice (cGMP) Certificate Training Program Course Which Are Organized By Pharmatec Pakistan (Ltd.) Under The Supervision of World-Renowned Name in Pharmaceutical Industry; Mr. Sultan Ghani; at Karachi, Sind – Pakistan; in 2017 * Attended An Operational Training of Hardness Tester Instrument PTB–311E Model From Rays Technologies; at Karachi; in 2016 * Completed Introduction to Good Clinical Practice (iGCP) Certificate Course From Physis Learning Academy (Pvt.) Ltd., at Calgary, AB – Canada; in 2016 * Completed of Internal Auditor And Risk Management Certificate Courses From Quality Gurus; at Calgary, AB – Canada; in 2016 * Completed of Six-Sigma White Belt Certificate Course From UDEMY; at Calgary, AB – Canada; in 2016 * Completed of The Quality Guru Certificate Course From Quality Gurus; at Calgary, AB – Canada; in 2016 * Completed Awareness of ISO 9001:2015 And Quality Management Courses From Quality Gurus; at Calgary, AB – Canada; in 2016 * Completed Certificate Course of Six Sigma White Belt From Aveda Business Institute; at Pennsylvania, PA 16066 – USA; in 2015 * Completed Awareness of ISO 9001:2008 Certificate Course From Quality Gurus; at Calgary, AB – Canada; in 2015 * Completed WHMIS Certificate Course From Canadian Centre For Occupational Health & Safety; at Hamilton, ON – Canada; in 2015 * Completed Series of Certificate Courses Which Are Includes First Aid Basic Certificate Course, Cardiopulmonary Resuscitation (CPR) Certificate Course, First Aid Advanced Certificate Course, Pediatric First Aid Certificate Course And Automated External Defibrillator (AED) Certificate Course From First Aid Online Course Provider; at Calgary, AB – Canada; in 2015 * Attended International Society of Automation (ISA) Conference & Show in Apr 22nd – 23rd, 2015 at Stampede Park, at Calgary, AB – Canada; in 2015 * Completed Safety Compliance: ANSI – MSDS Educational CD – ROM; Which Are Organized By MFS Canada Food Safety LLC; in 2011 * Attended Global Petroleum Conference & Show in June 10th – 12th, 2008; in June 09th – 11th, 2009; in June 08th – 10th, 2010; in June 07th – 09th, 2011; in June 12th – 14th, 2012; in June 11th – 13th, 2013; in June 10th – 12th, 2014; & in June 09th – 11th, 2015 & as Well as in June 07th – 09th, 2016; Respectively at Stampede Park, Calgary, – AB; Canada * Completed Health Safety & Compliance Course On Behavior Based Safety From Alison Institute, Ireland; in 2011 * Completed Series of Courses I’M ALERT Food Safety Training of Hygiene; Temperature Control; Healthy Food Handlers; Food Safety Programs; Pest Control; Cleanliness; Safe Food Storage & Disinfection From Clubs WA / Environmental Health Australia; in 2010 * Attended On Job Training of HSE, PPE & MSDS From Variperm; WEIDMANN at Calgary & From MFS at High River; AB – Canada * Completed Course of Emergency First Aid; From St. John Ambulance; Australia; in 2010 * Completed Course of Material Safety Data Sheet (MSDS); From ILPI, NJ 08012; USA in 2010 * Completed Courses of Hazard Communications; Safety & Health Programs; Personal Protective Equipment And Flammable & Combustible Liquids From Mastery Technologies Inc., MI 48375; USA; in 2010 * Completed Course of WHMIS Training From AIX Safety Toronto, Ontario – Canada; in 2010 * Completed Courses of ACPE Universal Program of New Drugs of 2007; New Drugs of 2008 & New Drugs of 2009 From Pharmacy Times Office of Continuing Professional Education, NJ 08536; USA; in 2010 * Completed Clinical Operations GCP – ICH Training Series – CAPA’s, From Norton Training Institute, SC 29072, USA; in 2010 * Completed Courses of GMP0 Documentation And Record Keeping; GCP0 Introduction to Clinical Trials And Drug Development And CTC0 Circulating Tumor Cells as Biomarkers From Bio Pharma Institute, NJ 07481, USA; in 2010 * Completed Six Weeks Course of Statistical Process Control From SAIT Polytechnic; Which Are Organized By Hunting Energy at Calgary – Alberta, Canada; in April 2009 * Completed The Course Study of Standard And Complaint Resolution Which Are Organized By Petro Canada; in 2006 * Attended Lectures On Chemistry Burying Carbon Dioxide in Underground Saline Aquifers Political Folly or Climate Change Fix? at The University of Calgary; Which Are Organized By ACPA – AB, Canada; in April 14th, 2010 * Attended (AGM) Form ACPA On May 09th 2009 at Calgary – AB; On May 03rd 2014 at Nisku – AB & On May 30th 2015; at Calgary – AB & On May 7th, 2016 at The Executive Royal Inn, Leduc, AB; Canada * Participation The Enrollments Contest & Achieving The Third Prize For The Top 10 GSA’s From Petro Canada; in 2007 * Certificate / Awards For The Best Employee of the Year From Petro Canada; in 2006 * Achieving The Certificate of Excellence of Highest Petro Points in The (Toronto) Territory, Organized By Petro Canada; in 2005 * Attended Training Course On Safety And First Aid at Petro Canada North York Center – Toronto; in 2004 * Achieved 10 Years Awards / Shield From Pharmaceutical Professional Club’s, at Karachi, Sind – Pakistan; in 2003 * Attended 4 Days 7th Eurasia Conference On Chemical Sciences Which Are Organized By HEJ Research Institute of Chemistry; International Center For Chemical Sciences; From University of Karachi; in 2002 PROFESSIONAL AFFILIATION * Fellow of The Association of Chemical Profession of Alberta (ACPA) P. Chem. # M 0532 – Since 2008 & Was Received Special Lapel Pin With The Joint Collaboration of UNO & ACPA, in July 2011; * Life Member of The Chemical Society of Pakistan; * Fellow of The Young Chemist Council; * Life Member of The Chemistry Alumni Welfare Association; * Ex-Member of The Pharmaceutical Professional Club’s; * Member of Stamp Quest Canada (#-); & Also Collect Stamps’, Coins & Bank Notes All Over The WORLD. COMPUTER’s SOFTWARE SKILLS * Computer Software Skills Proficiency Particularly in Microsoft Office (MS Word, Excel, Power Point, Outlook); * Management Tools: MS-Project; * Statistical Software, Scientific Software & Chromatographic Related Software’s e.g. JCL 6000 Data Chromatography System, LC-6 A, LC 10 A, CR-4A, CR – 6A, HPLC Agilent Quaternary Pump With Auto Sampler, Perkin Elmer HPLC Flexor Binary Pump With Auto Sampler And HPLC Auto Sampler of Knauer (AZURA), WinLIMSLink Method / AIM; WinELN Form / Labtronics, Qualink / Qualtrax, LIMS, SAP, Microsoft Dynamics – AX 2012; And Internet Browsing And Email etc. PERSONEL INFORMATION Father’s Name: Syed Masood Alam (Late) Place & Date of Birth: Karachi; October, 10, 1971 Nationality: Dual Citizen (Pakistani & Canadian) NICOP #: - Driver’s License: Having Intl Driver’s License Reference: Will be Furnished Upon Request
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