Quality Analyst I

Teva Pharmaceutical Industries Ltd.

Full Time
Posted 2 years ago

Job Features

Job CategoryOther Job, Software Jobs
Eligibility: M.Sc. in Chemistry, Bio - Chemistry, Microbiology, Biotechnology, M.Pharma –Quality Assurance or Pharmacology
Job Description• Review and check of all bioanalytical documents, method validation, bioanalytical report, statistical reports and clinical study report. • Review of protocol against applicable regulatory guidelines. • Review of relevant standard operating procedures to check compliance with regulatory guidelines and suggest appropriate modifications if any. • Preparation of standard operating procedures related to Bioanalytical Quality assurance department. • Retrieval of documents from archives as and when required. • Verification of system compliance of the system with respect to the standard operating procedures and other applicable regulatory requirements and to the response to the queries. • Aware on various regulatory guideline such FDA, EMA, ANVISA, GCP&GLP • Trending of CAPA • Review of validation and calibration of equipment and software • To carry out other responsibilities as and when assigned by the management
Job SummaryJob Type : Full Time Job Role : IT Software-Engineer Job Category : IT/Software Hiring Process : Face to Face Interview Who can apply : Freshers
Last Date to Apply01 Feb 2020
About CompanyTeva is a global pharmaceutical leader and the world's 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 world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.

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