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Md Marufur Rahman 
Unit1, 236Anzac highway, 
Plympton , SA 5038 
E-mail: maruf_76@yahoo.com 
Mob:0470691397 
Career Summary 
A pharmaceutical Professional in the arena of manufacturing medicine, Development, in 
process control and with over twelve years of experience, I have gained considerable 
experience working in various pharmaceutical track like GMP, validation and lastly in IQ OQ 
PQ, Process Validation. Defining professional attributes are strong problem solving skills, 
communication capacity together with the ability to work constructively with team members 
and auditors, and my knowledge and awareness of productivity and mission of regulatory 
affairs. 
Technical Expertise 
 Strong ability of writing documentation, standard operating procedures, protocols, 
validation and calibrations. 
 Experienced in productivity improvement, Kaizen, six sigma method certified by APO 
Asian productivity organization 
 Extensive knowledge in sterile product manufacturing (injection and ophthalmic 
products) 
 Experienced in GMP, cleaning validation, and sterilization 
 Experienced in using different tooling and techniques of blow fill seal machine. 
 Knowledge of Factory acceptance test, installation qualification (IQ) operational 
qualification (OQ) performance qualification( PQ) of machines 
 Basic understanding in PLC programmable logic controller 
 Expert in sterilizer (dry heat and moist heat sterilize) and freeze dryer. 
 Clear understanding of QA attributes ( in process control) Micro biological assays and 
so on. 
Professional Award/Achievement 
 APO Asian productivity Certified Professional. 
 Certificate of GMP training 
 Certificate of fire fighting training 
 First Aid and manual handling certificate 
 Training in conflict management 
 “Valuable contribution on successful commissioning of different machines of ” 
sterile production. Such as leak tester ( bubble point), CIP cleaning in place SIP 
sterile in place
Working Experience 
1. Currently working as a ware house assistant in chiller section in Baida group, 22 
Moss road Wing field SA since Jun 2013 to till date. 
2. Square Pharmaceuticals Limited Bangladesh 
(biggest Pharmaceuticals of Bangladesh. It is the c ountry’s largest medic ine 
manufacturer and distributer exporting to many other countries including UK.) It is 
approved by UK MHRA and TGA Australia 
Position: Senior Executive, Sterile product manufacturing 
Tenure: From January, 2008 to Feb, 2012 
Reasons of leaving: Migrating to Australia 
Responsibilities: 
 Ensure Product supply as per marketing requirement by using SAP software 
 To install and maintain Cold chain validation of temperature sensitive 
products 
 Run the production of SVPO plant with GMP compliance perform internal 
audit. and facing regulatory audit. 
 To deploy automated process of day to day reporting data transfer from 
production to report database through SAP. 
 Execute and supervise the compounding, CIP, SIP, filling, Sealing, visual 
inspection of Sterile liquid of SVPO plant from BFS (blow fill seal) Flexicon, 
Plumat and many other machineries 
 Preparation of BMR, BPR, Risk assessment protocol, Validation and 
Qualification documents and execution of validation protocols. Raise change 
control as when required 
 To Prepare of user requirement specification (URS) for new machineries 
 To Work with consultant Dr. Suggy (consultant) for FDA approval 
3. Renata Limited 
(Country’s one of the largest medicine manufacturer and it has 25 years of Pfizer 
USA in heritage, formerly this facility was Pfizer Bangladesh.) 
Position: Senior Officer, Production 
Tenure: From April, 2002 to Dec, 2007 
Reasons of leaving: To be introduced with biggest pharmaceutical of the country 
Responsibilities: 
 Preparation, Execute and training of BMR, BPR, SOP, Validation Protocols, 
change controls, and many other GMP documents. 
 In process check of manufacturing and packaging lines (conveyer belts) and 
calculate reconciliation of batch history management and administration. 
 To Prepare the EOP equipment operating procedure for process and machine. 
Monitor and notify and train alert to the operators. 
 Prepare monthly plan of production human and veterinary products and carry 
out the plan.
4 Orion infusions Limited 
A Large volume parenteral products (LVP) products manufacturer 
Position: Production Officer 
Tenure: From October, 2001 to April, 2002 
Reasons of leaving: Get opportunity to work for c ountry’s one of the best Sterile 
products manufacturer. 
Responsibilities: 
 To involve in preparing production Schedule, Ensure cleanliness of sterile area 
 To ensure workers/staffs gowning for their respective jobs 
 To Ensure all requests for” In proc ess test” are done timely and such test 
result to be incorporated in batch history. 
Education 
 Qualification: Masters in Pharmaceutical technology 
Institution: The University of Asia Pacific, Dhaka Bangladesh 
 Qualification: Bachelor (Hons) in pharmacy B.Pharm 
Institution: The University of Asia Pacific, Dhaka, Bangladesh 
Professional Training 
 Name of Training: on Communication and presentation skill 
Arranged By: Square Pharmaceuticals Limited 
Trainer: Impra consulting USA 
Duration: Day long 
 Name of Training: GMP training 
Arranged By: SQUARE pharmaceuticals 
Trainer: Dr Suggy chari 
Duration: 4 month 
 Name of Training: Productivity 
Arranged By: Asian Productivity Organization (APO) 
Trainer: Dr. Kawada, Mr. Masuzaki 
Duration: 3 days 
FOREIGN TRAINING& TOURS: 
SPAIN: 10 days visit in Barcelona, Spain for FAT ( Factory acceptance test) of Autoclave at 
Telster from 17 De’10 to 26 Dec ’10. www.tpro.es. During this time I also visited Paris as a 
tourist. 
CHINA: 4 days visit at Shanghai in China for Factory acceptance test for an Ampoule 
filling and sealing Machine. April 2006. www.shxufa.com 
CHINA: 5 days industrial tour at Shanghai in China to Visit different Machine Manufacturer 
like Freeze dryer ,Sandwich Pannell board, Sterile Tunnel for cephalosporin injection, Vial 
Ampoule filling and sealing Machine In October2005.www.jf-granulator.com, 
www.tofflon.com
INDIA:One week Industrial Training at Global Pharmatech Bangalore India in April 
2004 www.globalpharmatech.com 
Personal Information 
 Nationality: Bangladeshi 
 Residential Status: Australian Resident (Visa Subclass 475) 
 Australia Visa Status: Permitted to work, live and study. 
 Language Proficiency: 
o English: Fluent in all sort of communication. 
o Bengali: Mother Tongue. 
Referees 
Masum Mithu 
Validation Engineer, Mayne Pharma 
Mobile: 0423937540 
Dr. Md Zahurul Hossain 
Quality Assurance Manager 
Square Pharmaceuticals Ltd. 
Dhaka unit, Kaliakoir, Gajipur, Bangladesh 
+8801711889980(work) 
+8801713364956 (home) 
Email: zahurul@squaregroup.com

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UPdated CV Maruf

  • 1. Md Marufur Rahman Unit1, 236Anzac highway, Plympton , SA 5038 E-mail: maruf_76@yahoo.com Mob:0470691397 Career Summary A pharmaceutical Professional in the arena of manufacturing medicine, Development, in process control and with over twelve years of experience, I have gained considerable experience working in various pharmaceutical track like GMP, validation and lastly in IQ OQ PQ, Process Validation. Defining professional attributes are strong problem solving skills, communication capacity together with the ability to work constructively with team members and auditors, and my knowledge and awareness of productivity and mission of regulatory affairs. Technical Expertise  Strong ability of writing documentation, standard operating procedures, protocols, validation and calibrations.  Experienced in productivity improvement, Kaizen, six sigma method certified by APO Asian productivity organization  Extensive knowledge in sterile product manufacturing (injection and ophthalmic products)  Experienced in GMP, cleaning validation, and sterilization  Experienced in using different tooling and techniques of blow fill seal machine.  Knowledge of Factory acceptance test, installation qualification (IQ) operational qualification (OQ) performance qualification( PQ) of machines  Basic understanding in PLC programmable logic controller  Expert in sterilizer (dry heat and moist heat sterilize) and freeze dryer.  Clear understanding of QA attributes ( in process control) Micro biological assays and so on. Professional Award/Achievement  APO Asian productivity Certified Professional.  Certificate of GMP training  Certificate of fire fighting training  First Aid and manual handling certificate  Training in conflict management  “Valuable contribution on successful commissioning of different machines of ” sterile production. Such as leak tester ( bubble point), CIP cleaning in place SIP sterile in place
  • 2.
  • 3. Working Experience 1. Currently working as a ware house assistant in chiller section in Baida group, 22 Moss road Wing field SA since Jun 2013 to till date. 2. Square Pharmaceuticals Limited Bangladesh (biggest Pharmaceuticals of Bangladesh. It is the c ountry’s largest medic ine manufacturer and distributer exporting to many other countries including UK.) It is approved by UK MHRA and TGA Australia Position: Senior Executive, Sterile product manufacturing Tenure: From January, 2008 to Feb, 2012 Reasons of leaving: Migrating to Australia Responsibilities:  Ensure Product supply as per marketing requirement by using SAP software  To install and maintain Cold chain validation of temperature sensitive products  Run the production of SVPO plant with GMP compliance perform internal audit. and facing regulatory audit.  To deploy automated process of day to day reporting data transfer from production to report database through SAP.  Execute and supervise the compounding, CIP, SIP, filling, Sealing, visual inspection of Sterile liquid of SVPO plant from BFS (blow fill seal) Flexicon, Plumat and many other machineries  Preparation of BMR, BPR, Risk assessment protocol, Validation and Qualification documents and execution of validation protocols. Raise change control as when required  To Prepare of user requirement specification (URS) for new machineries  To Work with consultant Dr. Suggy (consultant) for FDA approval 3. Renata Limited (Country’s one of the largest medicine manufacturer and it has 25 years of Pfizer USA in heritage, formerly this facility was Pfizer Bangladesh.) Position: Senior Officer, Production Tenure: From April, 2002 to Dec, 2007 Reasons of leaving: To be introduced with biggest pharmaceutical of the country Responsibilities:  Preparation, Execute and training of BMR, BPR, SOP, Validation Protocols, change controls, and many other GMP documents.  In process check of manufacturing and packaging lines (conveyer belts) and calculate reconciliation of batch history management and administration.  To Prepare the EOP equipment operating procedure for process and machine. Monitor and notify and train alert to the operators.  Prepare monthly plan of production human and veterinary products and carry out the plan.
  • 4. 4 Orion infusions Limited A Large volume parenteral products (LVP) products manufacturer Position: Production Officer Tenure: From October, 2001 to April, 2002 Reasons of leaving: Get opportunity to work for c ountry’s one of the best Sterile products manufacturer. Responsibilities:  To involve in preparing production Schedule, Ensure cleanliness of sterile area  To ensure workers/staffs gowning for their respective jobs  To Ensure all requests for” In proc ess test” are done timely and such test result to be incorporated in batch history. Education  Qualification: Masters in Pharmaceutical technology Institution: The University of Asia Pacific, Dhaka Bangladesh  Qualification: Bachelor (Hons) in pharmacy B.Pharm Institution: The University of Asia Pacific, Dhaka, Bangladesh Professional Training  Name of Training: on Communication and presentation skill Arranged By: Square Pharmaceuticals Limited Trainer: Impra consulting USA Duration: Day long  Name of Training: GMP training Arranged By: SQUARE pharmaceuticals Trainer: Dr Suggy chari Duration: 4 month  Name of Training: Productivity Arranged By: Asian Productivity Organization (APO) Trainer: Dr. Kawada, Mr. Masuzaki Duration: 3 days FOREIGN TRAINING& TOURS: SPAIN: 10 days visit in Barcelona, Spain for FAT ( Factory acceptance test) of Autoclave at Telster from 17 De’10 to 26 Dec ’10. www.tpro.es. During this time I also visited Paris as a tourist. CHINA: 4 days visit at Shanghai in China for Factory acceptance test for an Ampoule filling and sealing Machine. April 2006. www.shxufa.com CHINA: 5 days industrial tour at Shanghai in China to Visit different Machine Manufacturer like Freeze dryer ,Sandwich Pannell board, Sterile Tunnel for cephalosporin injection, Vial Ampoule filling and sealing Machine In October2005.www.jf-granulator.com, www.tofflon.com
  • 5. INDIA:One week Industrial Training at Global Pharmatech Bangalore India in April 2004 www.globalpharmatech.com Personal Information  Nationality: Bangladeshi  Residential Status: Australian Resident (Visa Subclass 475)  Australia Visa Status: Permitted to work, live and study.  Language Proficiency: o English: Fluent in all sort of communication. o Bengali: Mother Tongue. Referees Masum Mithu Validation Engineer, Mayne Pharma Mobile: 0423937540 Dr. Md Zahurul Hossain Quality Assurance Manager Square Pharmaceuticals Ltd. Dhaka unit, Kaliakoir, Gajipur, Bangladesh +8801711889980(work) +8801713364956 (home) Email: zahurul@squaregroup.com