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CURRICULUM VITAE
BHUPENDRA SINGH
Email: bhupendraaeri@gmail.com
Contact No: +9690602346
Carrier Objective:
To achieve highest level in profession and to utilize my skills and abilities in the Healthcare sector
industry that offers professional growth while being resourceful, innovative, creative and flexible.
EDUCATIONAL QUALIFICATION :
 Master of Science (Biotechnology) (2016). with first division
Kumaun university (M.B GOVT P.G COLLEGE HALDWANI, UTTARAKHAND)
 Bachelor of Science (Biotechnology) (2014). Kumaun university (M.B GOVT P.GCollege,
Haldwani, Uttarakhand)
 Intermediate (PCB) (2011) UK Board.
 High School (2009) UK Board
PROFESSIONAL EXPERIENCE :
 AS QA trainee in Tulip diagnostic pvt.LTD. Rudrapur Uttarakhand July 2016 to June 2017
 As QA officer in J mitra & CO, Pvt. Ltd. New Delhi(A Medical device manufacturing
organization) from June 2017 to till date.
Key Responsibilities :-
Documentation (QMS)
 Document and data control , maintaining document related training (external/internal), internal
audit and MRM
 Preparation & review of QMS document ( SOPs,MFR,STP & Quality manual)
 Handling of deviation, change control ,OOS,OOT and CAPA
 Preparation of annual review & trend analysis
 Preparation , Review & implementation of CAPA
 Weekly inspection in RM store & engineering department.
IPQA activity
 IPQA activity in Manufacturing area (line clearance , shop floor verification ,Effectiveness of
SOPs Random process audit , sampling of intermediate /finished product.)
 Review of BMR/BPR
 Visual inspection of product at various level .
 Online review of various log books during production activity.
Validation & calibration:
 Calibration of measuring & monitoring Device (planner/Schedule preparation ,coordination of
external party for calibration and reviewing of calibration certificate )
 Preparation of Process Validation Protocol and Review of Process Validation Report.
 Qualification & documentation of HVAC system /clean room class –A,B,C & D/bio safety labs
including all test: Air velocity, HEPA filter integrity test , Partical count , Temperature
,differential pressure ( negative & positive pressure ) & Air flow pattern.
 Process validation /cleaning validation & documentation of all process : mixing filtration ,
washing , & drying filling labeling & coding, sealing & kit packing process
KNOWLEDGE ABOUT:-
 ISO 9001:2015
 ISO 13485 :2016
 5S
 SPC
Declaration:
I bhupendra singh do hereby declare that the above information given by me is true and correct in best of
my knowledge nothing Matter has been concealed.
Date: (Bhupendra singh)
Place:

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Cv (bhupendra singh)

  • 1. CURRICULUM VITAE BHUPENDRA SINGH Email: bhupendraaeri@gmail.com Contact No: +9690602346 Carrier Objective: To achieve highest level in profession and to utilize my skills and abilities in the Healthcare sector industry that offers professional growth while being resourceful, innovative, creative and flexible. EDUCATIONAL QUALIFICATION :  Master of Science (Biotechnology) (2016). with first division Kumaun university (M.B GOVT P.G COLLEGE HALDWANI, UTTARAKHAND)  Bachelor of Science (Biotechnology) (2014). Kumaun university (M.B GOVT P.GCollege, Haldwani, Uttarakhand)  Intermediate (PCB) (2011) UK Board.  High School (2009) UK Board PROFESSIONAL EXPERIENCE :  AS QA trainee in Tulip diagnostic pvt.LTD. Rudrapur Uttarakhand July 2016 to June 2017  As QA officer in J mitra & CO, Pvt. Ltd. New Delhi(A Medical device manufacturing organization) from June 2017 to till date. Key Responsibilities :- Documentation (QMS)  Document and data control , maintaining document related training (external/internal), internal audit and MRM  Preparation & review of QMS document ( SOPs,MFR,STP & Quality manual)  Handling of deviation, change control ,OOS,OOT and CAPA  Preparation of annual review & trend analysis  Preparation , Review & implementation of CAPA  Weekly inspection in RM store & engineering department.
  • 2. IPQA activity  IPQA activity in Manufacturing area (line clearance , shop floor verification ,Effectiveness of SOPs Random process audit , sampling of intermediate /finished product.)  Review of BMR/BPR  Visual inspection of product at various level .  Online review of various log books during production activity. Validation & calibration:  Calibration of measuring & monitoring Device (planner/Schedule preparation ,coordination of external party for calibration and reviewing of calibration certificate )  Preparation of Process Validation Protocol and Review of Process Validation Report.  Qualification & documentation of HVAC system /clean room class –A,B,C & D/bio safety labs including all test: Air velocity, HEPA filter integrity test , Partical count , Temperature ,differential pressure ( negative & positive pressure ) & Air flow pattern.  Process validation /cleaning validation & documentation of all process : mixing filtration , washing , & drying filling labeling & coding, sealing & kit packing process KNOWLEDGE ABOUT:-  ISO 9001:2015  ISO 13485 :2016  5S  SPC Declaration: I bhupendra singh do hereby declare that the above information given by me is true and correct in best of my knowledge nothing Matter has been concealed. Date: (Bhupendra singh) Place: