Girish Hirpara

Angestellt, Manager Regulatory Affairs, Quality Assurance and Clinical Affairs, Biotechni SAS

Skills

Regulatory Affairs
Quality Management
Clinical Research
Medical Device Regulation (MDR)
Pharmaceutical Regulatory
ISO 13485
EUMDR 2017/745
US FDA 510K
MDSAP
ANVISA
HEALTH CANADA
QMS
VEEVA VAULT
Change Control
Technical Documentation

Timeline

Professional experience for Girish Hirpara

  • Current 6 years and 2 months, since Sep 2020

    Manager Regulatory Affairs, Quality Assurance and Clinical Affairs

    Biotechni SAS

  • 3 years and 9 months, Jan 2017 - Sep 2020

    Sr. Manager- Regulatory & Clinical Affairs

    Biotech Vision Care Pvt Ltd

  • 5 years and 10 months, Apr 2011 - Jan 2017

    Regulatory & Clinical Affairs Manager

    Meril Life Sciences Pvt Ltd.

    Regulatory & Clinical Affairs Manager

  • 4 years and 5 months, Dec 2006 - Apr 2011

    Asst. Manager – Clinical Affairs

    BA Research India Ltd

Languages

  • English

    C2 (Expert / native speaker)

XING – The jobs network

  • Over 1 million jobs

    Find just the right job for you on XING.

  • Job offers just for you

    Get found by employers and over 20,000 recruiters.

  • 21 million members

    Connect with new people and gather inspiration to boost your working life.

  • Free membership

    Basic membership is free, but the opportunities are priceless.

Browse over 21 million XING members