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Syed Muhammad Tabish
INTRODUCTION
A well professional personnel having around 9 years of work experience in different areas of
Quality Operation in a world leading multinational pharmaceutical (Pfizer, Wyeth, Pharmacia,
Park Davis ) and certification company (SGS) . During my career I have experienced several
corporate GMP / EHS / Laboratory audits several local ministry representatives visits and
represent QO in company EHS and GMP related meetings. Although I have very strong command
over all aspect of QA and audits yet I believe in continuous learning and helping my colleagues to
explore a new dimension of work every day.
AREA OF EXPERTIES
 QMS ISO 9001 audits
 GMP/GLP/GDP audits
 ICH/WHO/FDA guidelines
 Laboratory management system
 Good laboratory practices
 EHS audits
 CAPA
 Investigations and Deviations
 Change Management
 Human Error Reduction
 Process supervision
 Process Improvement
 Market Actions
 Process Capability
 GMP Compliance
 System Creation
WORKING EXPERIENCE
Present Experience
Currently working in SGS Pakistan as Lead Auditor /Tutor since 08 sept 2014 , Till date I have
conducted more than 150 2nd
party/3rd
party audits and trainings on different standards like ISO
9001:2015,ISO 22716,GMP pharma, GDPMD, GDP pharma standards , ISO 17025 standards in
different healthcare industry including pharmaceuticals, clinical labs and hospitals .
Previous Experience
Previously worked in Quality Operations as Senior. QA officer (GMP Compliance), since Feb 2009 in
Pfizer Global Supply till 05 sept 2015 during my tenure had been involved in system integration of
Pfizer with Pharmacia, Wyeth and Park devis furthermore, I had also been involve in WHO project of
Wyeth Pakistan as project coordinator .My main task in Pfizer was to conduct GMP / EHS audit of PD
and Wyeth sites furthermore I had also been involve in supplier audits.
JOB RESPONSIBILITIES In Pfizer Pakistan 16 Feb 2009 till 05 sep 2014:
 Assist QA Manager in market complaints and investigation.
 Assist QA Manager in conducting the Audits of Distributors ware houses and vendors and
suppliers
 To conduct GMP audits and trainings
 Design, develop and implement Quality standard as per global and local regulatory
guidelines.
 Key opinion leader in process improvement projects.
 Having active participation in developing lean process and to reduce waste.
 Member of spill control team
 To assist audit team in the internal and external audits and measuring compliance with
the company's HSEQ rules and regulations and local regulatory standards.
 Responsible to implement and follow the EHS procedures, policies and practices in
Warehouse, Production and QO areas.
 To represent QO dept in monthly EHS meeting.
 Member of supplier management team.
 To conduct mock recall (distribution channel intelligence).
 To conduct Laboratory audit
 SOP update
 To prepare Annual Product review reports (APRR)
 Responsible to maintain the files and records of all Products, Batch Documents History,
Current Master copies of SOPs, Current Master Batch Documents, Receiving Reports,
Obsolete SOPs, Obsolete Batch Documents, Product Registration, all Investigation reports.
PCP/PCR, Deviation Report, Local Change Management and Product Change
Management....
 Responsible to accept the tasks assigned by Departmental Manger other than regular
activities.
ACADEMIC CREDENTIALS
Year Degree Specialization Institution
2008 MSc.
Chemistry
Karachi University
2013 MBA Marketing Iobm
ERP (Software’s) Awareness
 Oracle Web Based Inventory Software.
 NIPS Web Based Inventory Management Software.
 DAS – Bar-coding Dispensing Automation System.
 MAPS (Manufacturing, Accounting, & Planning System) ERP (AS400) Software.
 SMS (supplier Management system )
SKILLS & COMPETENCIES:
Technical:
 Local as well as international quality guidelines.
 Human Error Reduction
 Knowledge of regulatory registration process, DRAP/ WHO,ICHFDA guidelines
 GMP / EHS auditing
 Laboratory management
 Infection prevention and control
 Patient safety
Personal:
 Creative and innovative
 Ability to think strategically
 Strong communication and presentation skills
 Sound decision-making capability
 Strong analytical skills
 Time management
TRANINGS AND CERTIFICATION
 IRCA registered ISO:9001:2008 QMS lead auditor course from SGS Pakistan (Oct 2014)
 Training session on ISO 9001:2015 version
 Certified Pharmaceutical GMP Professional
 Pharmacovigilance in healthcare
 2 days training course on ISO 17025 Lab accreditation
 2 days training session on ISO 22716 GMP cosmetic.
 Six sigma green belt trained.
 Six sigma yellow belt certified
 Pfizer Integrity Pledge
 Document hold global training
 Anti-Bribery and Anti corruption Procedure
 Foreign Corrupt Practices Act
 Human Error Reduction Sciences
 Fire & Safety training (conducted by EHS Department of Pfizer)
OPERATIONAL EXCELLENCE PROJECTs Yellow belt projects:
A) Problem Definition
Harmonization of in-process of three legacies (Pharmacia, Parke Davis & Pfizer)- improvement in in-process
result system
B) Problem Definition
Reduction in human error by using human error sciences.
C) Problem Definition
Delays in submission of “Before Decision” and finished good reports from QC to QA
D) Problem Definition
Reduce the lead time for batch release
PERSONAL INFORMATION
Father’s Name: Syed Muhammed Zia uddin
Address: A-945 Sector 11-A Karachi Pakistan
NIC: 42101-3937515-5
Contact: CELL # +92320-5517618
+923232431539
E-Mail: Tabish.syed@ymail.com
Date of Birth 27-sept-1984

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Tabish resume

  • 1. Syed Muhammad Tabish INTRODUCTION A well professional personnel having around 9 years of work experience in different areas of Quality Operation in a world leading multinational pharmaceutical (Pfizer, Wyeth, Pharmacia, Park Davis ) and certification company (SGS) . During my career I have experienced several corporate GMP / EHS / Laboratory audits several local ministry representatives visits and represent QO in company EHS and GMP related meetings. Although I have very strong command over all aspect of QA and audits yet I believe in continuous learning and helping my colleagues to explore a new dimension of work every day. AREA OF EXPERTIES  QMS ISO 9001 audits  GMP/GLP/GDP audits  ICH/WHO/FDA guidelines  Laboratory management system  Good laboratory practices  EHS audits  CAPA  Investigations and Deviations  Change Management  Human Error Reduction  Process supervision  Process Improvement  Market Actions  Process Capability  GMP Compliance  System Creation WORKING EXPERIENCE Present Experience Currently working in SGS Pakistan as Lead Auditor /Tutor since 08 sept 2014 , Till date I have conducted more than 150 2nd party/3rd party audits and trainings on different standards like ISO 9001:2015,ISO 22716,GMP pharma, GDPMD, GDP pharma standards , ISO 17025 standards in different healthcare industry including pharmaceuticals, clinical labs and hospitals .
  • 2. Previous Experience Previously worked in Quality Operations as Senior. QA officer (GMP Compliance), since Feb 2009 in Pfizer Global Supply till 05 sept 2015 during my tenure had been involved in system integration of Pfizer with Pharmacia, Wyeth and Park devis furthermore, I had also been involve in WHO project of Wyeth Pakistan as project coordinator .My main task in Pfizer was to conduct GMP / EHS audit of PD and Wyeth sites furthermore I had also been involve in supplier audits. JOB RESPONSIBILITIES In Pfizer Pakistan 16 Feb 2009 till 05 sep 2014:  Assist QA Manager in market complaints and investigation.  Assist QA Manager in conducting the Audits of Distributors ware houses and vendors and suppliers  To conduct GMP audits and trainings  Design, develop and implement Quality standard as per global and local regulatory guidelines.  Key opinion leader in process improvement projects.  Having active participation in developing lean process and to reduce waste.  Member of spill control team  To assist audit team in the internal and external audits and measuring compliance with the company's HSEQ rules and regulations and local regulatory standards.  Responsible to implement and follow the EHS procedures, policies and practices in Warehouse, Production and QO areas.  To represent QO dept in monthly EHS meeting.  Member of supplier management team.  To conduct mock recall (distribution channel intelligence).  To conduct Laboratory audit  SOP update  To prepare Annual Product review reports (APRR)  Responsible to maintain the files and records of all Products, Batch Documents History, Current Master copies of SOPs, Current Master Batch Documents, Receiving Reports, Obsolete SOPs, Obsolete Batch Documents, Product Registration, all Investigation reports. PCP/PCR, Deviation Report, Local Change Management and Product Change Management....  Responsible to accept the tasks assigned by Departmental Manger other than regular activities. ACADEMIC CREDENTIALS Year Degree Specialization Institution 2008 MSc. Chemistry Karachi University 2013 MBA Marketing Iobm
  • 3. ERP (Software’s) Awareness  Oracle Web Based Inventory Software.  NIPS Web Based Inventory Management Software.  DAS – Bar-coding Dispensing Automation System.  MAPS (Manufacturing, Accounting, & Planning System) ERP (AS400) Software.  SMS (supplier Management system ) SKILLS & COMPETENCIES: Technical:  Local as well as international quality guidelines.  Human Error Reduction  Knowledge of regulatory registration process, DRAP/ WHO,ICHFDA guidelines  GMP / EHS auditing  Laboratory management  Infection prevention and control  Patient safety Personal:  Creative and innovative  Ability to think strategically  Strong communication and presentation skills  Sound decision-making capability  Strong analytical skills  Time management TRANINGS AND CERTIFICATION  IRCA registered ISO:9001:2008 QMS lead auditor course from SGS Pakistan (Oct 2014)  Training session on ISO 9001:2015 version  Certified Pharmaceutical GMP Professional  Pharmacovigilance in healthcare  2 days training course on ISO 17025 Lab accreditation  2 days training session on ISO 22716 GMP cosmetic.  Six sigma green belt trained.  Six sigma yellow belt certified  Pfizer Integrity Pledge  Document hold global training  Anti-Bribery and Anti corruption Procedure  Foreign Corrupt Practices Act  Human Error Reduction Sciences  Fire & Safety training (conducted by EHS Department of Pfizer)
  • 4. OPERATIONAL EXCELLENCE PROJECTs Yellow belt projects: A) Problem Definition Harmonization of in-process of three legacies (Pharmacia, Parke Davis & Pfizer)- improvement in in-process result system B) Problem Definition Reduction in human error by using human error sciences. C) Problem Definition Delays in submission of “Before Decision” and finished good reports from QC to QA D) Problem Definition Reduce the lead time for batch release PERSONAL INFORMATION Father’s Name: Syed Muhammed Zia uddin Address: A-945 Sector 11-A Karachi Pakistan NIC: 42101-3937515-5 Contact: CELL # +92320-5517618 +923232431539 E-Mail: Tabish.syed@ymail.com Date of Birth 27-sept-1984