Quality Control Analyst Job Opening 2019 @ Teva

="text-align: center;">Quality Control Analyst Job Opening 2019 @ Teva

Teva hiring Chemistry candidates for the post Quality Control Technician.Teva Hiring Postgraduate Chemical Science candidates. Teva is a global pharmaceutical leader and the world’s largest generic medicines producer committed to improving health. Interested candidates check out all the relevant details. Check out all the details on the same below:

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 Control

Job Description: Quality Control Analyst I

Role and Responsibilities:

  • Performing Stability analysis, Method transfer and Method Validation.
  • Preparation and review of Method Transfer Protocols, Standard Testing Procedure,
  • Specifications, Test Data Sheet for Stability Analysis, Method transfer and Method Validation, Stability Summary Reports and any document related to stability analysis, method transfer and method validation in compliance with current guidelines. Review and maintenance of all logbooks of the department
  • Preparation of departmental SOP’s in compliance with current guidelines. Review of departmental SOP’s, training of analysts and other technical staff and review validation of data transfer, data management using computer systems.
  • Preparation and review of validation protocols in compliance with current guidelines.
    Calibration and validation of all instruments /equipment.
  • Procurement of columns, chemicals/ reagents/ solvents and standards for various stability analysis, method transfer and method validations.

Qualifications

  • Must have prior experience in analysis stability, finished samples handling of HPLC, GC and Dissolution.
  • Ability to be performance/target/goal-oriented.
  • Must have 4- 7 years of work experience in Quality Control Formulations
  • Must be a Post Graduate in Industrial Chemistry/B.Pharm or M.Sc.
  • Must possess good communication skills and be performance-driven

Apply Online

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