Teva Chemistry Quality Analyst Job Opening - Apply Online

Teva Chemistry Quality Analyst Job Opening – Apply Online

Chemistry Quality Analyst Analyst Job. Teva hiring Chemistry candidates for the post.Teva Hiring Undergraduate Chemical Science candidates. Teva is a global pharmaceutical leader and the world’s largest generic medicines producer committed to improving health. Teva Chemistry QA Job opening. Check out all the details on the same below:

Teva 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.

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Job Title: Quality Analyst

Location: Bangalore, IN, 560052

Qualifications

M.Sc. in Chemistry, 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
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  • Review of validation and calibration of equipment and software
  • To carry out other responsibilities as and when assigned by the management

Apply Online

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