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Quality Analyst I - 1312

Date: Mar 15, 2019

Location: Goa, IN, 403722

Company: Teva Pharmaceuticals

Company Info

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. 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.  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

  • Preparation for Method Validation protocol, approval and execution for validation.
  • Method validation for Assay, Identification, UOC, Dissolution and IDD.
  • Preparation for Method Validation summary reports.
  • Method development for Assay, Identification, UOC, Dissolution.
  • Preparation for Method Development reports and test methods.
  • Qualification of new Instruments and equipment.
  • cGMP compliance in the laboratory and work place.
  • To ensure compliance to the requirements of site procedures on Data integrity in GxP data handling.
  • Empower dynamic review and E signature
  • Record details of work done and results according to procedures and SOPs.
  • Daily and monthly calibration for analytical balances and pH meters.
  • Effective utilization of resources.
  • Follow the safety practices.
  • Follow the good documentation system requirements.
  • General cleanliness of the laboratory.
  • Sample receipt, verification, entry in register and storage at appropriate condition.
  • SOP list maintenance & SOP hard copy retrieval, file maintenance, Replace the old copies.

Qualifications

Master of Science

2 to 3 Years of Experience

Function

Quality

Sub Function

Quality Assurance Methods

Reports To

Group Leader Quality Functions

Competencies

5. Functional - Key functional requirements set by hiring manager

Teva’s Equal Employment Opportunity Commitment

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.