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CURRICULAM VITAE
PERSONAL DETAIL:
Name:Sayan Biswas
E-mail id:biswassayan7474@gmail.com
Contact no : 9742876711
EDUCATIONAL QUALIFICATION:
DEGREE LEVEL YEAR SCORE
1. ICSE 2005 83.6 %
2. ISC 2007 85.6%
3. B.E.( Medical Instrumentation) 2011 9.00 (CGPA)
WORK EXPERIENCE:
COMPANY1: Larsen & Toubro Ltd. – Medical Device &Equipment Division
Joining Date: 1st July 2011
End date:17th January 2013
Location: Mysore
Job Role: Project Engineer
COMPANY 2: Skanray Technologies Pvt. Ltd. – Healthcare Divisions
Joining Date: 18th January 2013
End date: Till Date
Location: Mysore
Job Role: Project Engineer
JOB DESCRIPTION:
 Development of Product. Project co-ordination between User Interface developers and Data
Acquisition System developers, hardware teams and other cross functional teams as required for
the development of the product.
 Understanding of the Application.
 Change Management activities.
 Cross Functional Team Activities
 Coordination with the Quality Team for product testing, verification & validation.
 Understanding of the bugs reported and getting it resolved.
 Review of QA reports.
 To keep track of the problems faced in Production and to resolve it.
 To interact with the Cross Functional Team from planning of the Pilot lot till the roll out of the
1st Production lot.
 Field trials for the testing units.
 Documentation
 To prepare, maintain & update the various documents for the product.
For e.g.: Bill of Material, Risk Management File, and Design Requirement Specification &
Software Requirement Specifications of the product.
 To prepare and provide the required documents for FDA & CE certification.
 To provide inputs for the documentation of Operating Manual & Service Manual to the
respective teams.
 Post Design Release
 To conduct training sessions for the service & marketing engineers to explain the product and
its application.
 To conduct field trials, interact with doctors and end users and to get their feedback.
 To discuss the feedback with the team and to implement the same, where feasible.
 To attend to the field reported problems and co-ordinate with the hardware/software teams
where required.
 Interaction with the Marketing team, planning for the product trials and demo.
 Review of the sales brochures and pamphlets.
 Standards
 Understanding of ISO14971 standard.
 Acquainted with ISO13485 standard.
 Adequate knowledge of IEC62304 standard.
 Overview of the AAMI standard.
 Testing for 60601-2-25
 Projects
 Multi parameter Patient Monitoring System
 ECG machine
 Cardiac Stress Test Setup ( Cardiac Treadmill )
 Other Projects
 To understand the implementation & application of the Cardiac Output (CO) module.
 To give demo and conduct field trials of the module.
 To train the Marketing & Service team about CO.
 To compare and select an alternative display for a product.
 Software skills
 MS Office
 C , C ++
 Training Received
 Quality System Regulation 21 CFR 820

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SayanBiswas- Resume

  • 1. CURRICULAM VITAE PERSONAL DETAIL: Name:Sayan Biswas E-mail id:biswassayan7474@gmail.com Contact no : 9742876711 EDUCATIONAL QUALIFICATION: DEGREE LEVEL YEAR SCORE 1. ICSE 2005 83.6 % 2. ISC 2007 85.6% 3. B.E.( Medical Instrumentation) 2011 9.00 (CGPA) WORK EXPERIENCE: COMPANY1: Larsen & Toubro Ltd. – Medical Device &Equipment Division Joining Date: 1st July 2011 End date:17th January 2013 Location: Mysore Job Role: Project Engineer COMPANY 2: Skanray Technologies Pvt. Ltd. – Healthcare Divisions Joining Date: 18th January 2013 End date: Till Date Location: Mysore Job Role: Project Engineer
  • 2. JOB DESCRIPTION:  Development of Product. Project co-ordination between User Interface developers and Data Acquisition System developers, hardware teams and other cross functional teams as required for the development of the product.  Understanding of the Application.  Change Management activities.  Cross Functional Team Activities  Coordination with the Quality Team for product testing, verification & validation.  Understanding of the bugs reported and getting it resolved.  Review of QA reports.  To keep track of the problems faced in Production and to resolve it.  To interact with the Cross Functional Team from planning of the Pilot lot till the roll out of the 1st Production lot.  Field trials for the testing units.  Documentation  To prepare, maintain & update the various documents for the product. For e.g.: Bill of Material, Risk Management File, and Design Requirement Specification & Software Requirement Specifications of the product.  To prepare and provide the required documents for FDA & CE certification.  To provide inputs for the documentation of Operating Manual & Service Manual to the respective teams.
  • 3.  Post Design Release  To conduct training sessions for the service & marketing engineers to explain the product and its application.  To conduct field trials, interact with doctors and end users and to get their feedback.  To discuss the feedback with the team and to implement the same, where feasible.  To attend to the field reported problems and co-ordinate with the hardware/software teams where required.  Interaction with the Marketing team, planning for the product trials and demo.  Review of the sales brochures and pamphlets.  Standards  Understanding of ISO14971 standard.  Acquainted with ISO13485 standard.  Adequate knowledge of IEC62304 standard.  Overview of the AAMI standard.  Testing for 60601-2-25  Projects  Multi parameter Patient Monitoring System  ECG machine
  • 4.  Cardiac Stress Test Setup ( Cardiac Treadmill )  Other Projects  To understand the implementation & application of the Cardiac Output (CO) module.  To give demo and conduct field trials of the module.  To train the Marketing & Service team about CO.  To compare and select an alternative display for a product.  Software skills  MS Office  C , C ++  Training Received  Quality System Regulation 21 CFR 820