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Quality Analyst I

3.00 to 6.00 Years   Bangalore   24 Mar, 2020
Watson Pharma Private Limited
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaSales / BD
EmploymentTypeFull-time

Job Description

Teva is a global pharmaceutical leader and the worlds largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and weve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient - centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth! Job Description

  • Check for compliance of study related activities to good clinical practice, concerned standard operating procedures and protocol.
  • Maintain obsolete clinical and medical diagnostic service standard operating procedures, and working documents relating to the same departments.
    • Verification and review of all bioequivalence/bioavailability study reports. Preparation/ review of standard operating procedures related to clinical quality assurance. Conducting facility and quality system audits.
  • Review of documents to ensure compliance with respect to validation and calibration of clinical instruments and software as per standard operating procedure and validation master plan.
    • To maintain computer system for electronic distributions. Periodic check of log books. Issue of log books & forms and maintaining inventory of log books.
  • To check the log book format with the approved log book template, maintain master and obsolete copies of the log book templates.
    • Verification of standard operating procedures maintained on computer system for electronic distribution/access Review of temperature and humidity records Preparation of standard operating procedures related to the clinical quality assurance department. Qualifications

    Education Qualification: - M.Pharm, B.Pharm, M.Sc.,

    R&D Quality In process of validation ,

    Keyskills :
    qualitycustomer relations test casescalibration auditinggood clinical practice researchdevelopment

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