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Executive-QA Manipal India, Mangaluru India,  

Navitas Life Sciences (company)


Posted on : 22 December 2017

Project Description

Category: Executive
Location: Manipal and Mangalore
Job Type:
Full Time
Education: B.Pharma or M.Pharma

Job Description:

  • In-process and retrospective GCP compliance audits for clinical studies
  • SOP preparation, review and implementation
  • Documentation and maintenance of SOPs, Process documents for BA/BE
  • Preparedness for External Audits & timely closure of audit observations
  • Review of Clinical study protocols, Informed consent documents, Clinical Study Reports
  • Quality check of raw data(CRFs), communication of observations and follow up with operational team for closure of the same
  • Ensure close looping of BA/BE Clinical & client audit observations as per the Timeline
  • Document control and change control management
  • Root cause analysis and CAPA
  • Conducting Internal Quality Audits/System audits (IQA)


Preferred Skills:

  • Preferably 1to 4 years of experience as a Research Associate or as a Clinical QA or Bio-Analyst or as a Bioanalytical QA


If you would like to apply for this position, or would like a discussion about this, or any other role, please send your contact details, together with your curriculum vitae to:
recruitment.manipal@navitaslifesciences.com

Locations

ManipalMangalore India

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