Hoshiyar Singh

Hoshiyar Singh Email and Phone Number

Department Head QC (Deputy Manager) at Uni Medicolabs Pvt.Ltd. @ Uni Medicolabs
Delhi, Delhi, IN
Hoshiyar Singh's Location
Dehradun, Uttarakhand, India, India
About Hoshiyar Singh

With over 21 years of experience in quality control and compliance, I am a competent and reliable professional who leads the quality control department at Uni Medicolabs a pharmaceuticals company based in Dehradun Uttarakhand. I have significant experience in Multicultural and multinational environments working with various regulatory agencies and standards such as WHO, USFDA, MHRA, TGA, EU etc.I have expertise in implementing good laboratory practices and maintaining compliance in the lab with respect to quality events, investigations and reports.I have exposure of different dosages forms such as Oral solid dosages, Injectables, Dry powder for Injectables, Aerosols, Nasal drops, Eye drops, Sachets etc.I am proficient in using various software tools such as SAP, Proteus, LIMS (Labware) Cipdox, Track wise, QCMS etc.I am passionate about ensuring the quality and safety of Pharmaceutical products and services. I strive to continuous improvement and innovate in my field.

Hoshiyar Singh's Current Company Details
Uni Medicolabs

Uni Medicolabs

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Department Head QC (Deputy Manager) at Uni Medicolabs Pvt.Ltd.
Delhi, Delhi, IN
Employees:
34
Hoshiyar Singh Work Experience Details
  • Uni Medicolabs
    Head Qc (Deputy Manager Qc)
    Uni Medicolabs Mar 2020 - Present
    Dehradun, Uttarakhand, India
    Handling of Quality control team for the routine activities purpose.Monitoring and guidance of the QC team on a daily basis for interaction and meeting for execution of routine activity.Daily meet for cross-functional departments for effective functioning and proper utilization of resources.Responsible for release of finished products, raw materials, packing materials with compliance to meet the data integrity.QC lead for proper investigations of quality managements system (QMS)like Incidents, OOS, OOT, Deviations etc. with tools such as 5-why, Fishbone etc.  To find out the root cause and fix a corrective and preventive maintenance for the same.Effectiveness of the CAPA.Responsible for managing overall operations of the QC lab with focus on resources management like procurement of impurities, WS, columns, having clearly defined Specifications, Standard Testing Procedures test data sheets for smooth functioning.Responsible for AMV as per ICH guideline, technology transfer of the products.To manage QMS activities like change control, deviations, can be completed within time.Team build up for audit and compliance purposes.To create goals, objectives and measures to drive continuous improvement of the QC resources.To ensure system and procedures are in place for the data integrity, carryout frequent checks and challenges tests to maintain compliance and consistency in data security, storage archival verification and originality.Analysing quality variance and implementing corrective and preventive action to maintain quality parameters.Responsible to review SOP, protocols as per cGMP. Responsible to plan out all QC resources and activities in relation and company objectives and set targets.Providing on job training to new entrants and performing analyst qualifications.Responsible for ensuring AMC/CMC of all the QC instruments and proper coordination for preventive maintenance and calibration of QC instruments.
  • Cipla
    Deputy Manager Qc
    Cipla Jul 2016 - Jul 2019
    Indore, Madhya Pradesh, India (Unit Ii Aersosol)
    Responsible for planning and execution of all the chromatographic (HPLC/GC) analysis for Finished Products, Stability, Raw materials, WS qualifications, calibrations etc.Daily coordination with cross-functional sections for smooth advance planning to meet the plant requirement.Monitored adherence to quality systems compiled with quality standards and maintained requisite documents.Responsible for plan investigation of OOS, OOT, incidents and experimental, hypothetical planning for find out the root cause for the same with coordination of cross-functional sections and LAB QA.Timely completion of investigations for release of the Product/material and fix the root cause and implementation for the same.Team build up for audit and compliance purposes.To create goals, objectives and measures to drive continuous improvement of the QC resources.To ensure system and procedures are in place for the data integrity, carryout frequent checks and challenges tests to maintain compliance and consistency in data security, storage archival verification and originality.Responsible to plan out all QC resources and activities in relation and company objectives and set targets.Providing on job training to new entrants and performing analyst qualification.Responsible for ensuring AMC/CMC of all the QC instruments and proper coordination for breakdown, preventive maintenance and calibration of QC instruments.Responsible for coordination with service engineers for minimum down time of the instruments.Responsible for management, procurement, qualification, regeneration and destruction of HPLC/GC columns.
  • Cipla
    Deputy Manager Qc
    Cipla Aug 2010 - Jul 2016
    Indore, Madhya Pradesh, India (Unit Iv Osd)
    Responsible for planning and execution of all the chromatographic (HPLC/GC) analysis for Finished Products, Stability, Raw materials, WS qualifications, calibrations etc.Daily coordination with cross-functional sections for smooth advance planning to meet the plant requirement.Monitored adherence to quality systems compiled with quality standards and maintained requisite documents.Responsible for plan investigation of OOS, OOT, incidents and experimental, hypothetical planning for find out the root cause for the same with coordination of cross-functional sections and LAB QA.Timely completion of investigations for release of the Product/material and fix the root cause and implementation for the same.Team build up for audit and compliance purposes.To create goals, objectives and measures to drive continuous improvement of the QC resources.To ensure system and procedures are in place for the data integrity, carryout frequent checks and challenges tests to maintain compliance and consistency in data security, storage archival verification and originality.Responsible to plan out all QC resources and activities in relation and company objectives and set targets.Providing on job training to new entrants and performing analyst qualification.Responsible for ensuring AMC/CMC of all the QC instruments and proper coordination for breakdown, preventive maintenance and calibration of QC instruments.Responsible for coordination with service engineers for minimum down time of the instruments.Responsible for management, procurement, qualification, regeneration and destruction of HPLC/GC columns.
  • Ipca Laboratories Limited
    Executive Qc
    Ipca Laboratories Limited Dec 2006 - Jul 2010
    Dehradun, Uttarakhand, India
    Responsible for all planning and execution of Finished Products, WS qualifications, calibrations etc.Daily coordination with cross-functional departments for smooth advance planning for production requirement and dispatches of finished goods.Monitored adherence to quality systems compiled with quality standards and maintained requisite documents.Responsible for plan investigation of OOS, OOT, incidents and experimental, hypothetical planning for find out the root cause for the same with coordination of cross-functional sections and LAB QA.Timely completion of investigations for release of the Product/material and fix the root cause and implementation for the same.Team build up for audit and compliance purposes.                                                                                                                                         To create goals, objectives and measures to drive continuous improvement of the QC resources.                                                                                                                                             Responsible to plan out all QC resources and activities in relation and company objectives and set targets.Providing on-job training to new entrants and performing analyst qualifications.                                   Responsible for ensuring AMC/CMC of all the QC instruments and proper coordination for breakdown, preventive maintenance and calibration of QC instruments.Responsible for coordination with service engineers for minimum down time of the instruments.Responsible for management, procurement, qualification, regeneration and destruction of HPLC/GC columns.Technology transfer from corporate for smooth analytical activities at plant.
  • Jocund India Limited
    Senior Qc Analyst
    Jocund India Limited Feb 2006 - Nov 2006
    Haridwar, Uttarakhand, India
    Analysis of Finished ProductsAnalysis of Bulk/semi finished productsAnalysis of Packaging materialsIn process of Quality control.Sampling of Raw Materials/Packaging materials
  • Aimil Pharmaceuticals ( India )Ltd
    Qc Analyst
    Aimil Pharmaceuticals ( India )Ltd Jan 2005 - Feb 2006
    Delhi, India
    Analysis of Finished ProductsAnalysis of Bulk/semi finished productsAnalysis of Packaging materialsIn process of Quality control.Sampling of Raw Materials/Packaging materials
  • Shreechem Pharmaceuticals Pvt Ltd
    Qc Chemist
    Shreechem Pharmaceuticals Pvt Ltd Jul 2002 - Dec 2004
    Navi Mumbai, Maharashtra, India
    Analysis of Finished Products.Analysis of Bulk/semi finished products.Analysis of Packaging materials.In process of Quality control.Sampling of Raw Materials/Packaging materials.

Hoshiyar Singh Education Details

Frequently Asked Questions about Hoshiyar Singh

What company does Hoshiyar Singh work for?

Hoshiyar Singh works for Uni Medicolabs

What is Hoshiyar Singh's role at the current company?

Hoshiyar Singh's current role is Department Head QC (Deputy Manager) at Uni Medicolabs Pvt.Ltd..

What schools did Hoshiyar Singh attend?

Hoshiyar Singh attended Dr. B. N. Bandodkar College Of Science Thane Mumbai, Dr. Bhim Rao Ambedkar University, Agra.

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