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Quality Analyst II - 6008

Date: Jun 10, 2021

Location: Haarlem, NL, 2031

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

The Senior Quality Analyst Document Controller supports high standards of quality at the department through continuously improving the effectiveness of the department quality processes and systems.

Responsibilities

  • Share best practices, challenges and lessons learned at the site in order to improve the performance of quality
  • Support a culture of enhancing quality throughout the entire site operation
  • Develop the technical expertise, personal skills and interpersonal skills needed to perform duties in line with Site expectations
  • Support an effective internal communications structure with relevant departments
  • Coordinate the performance of the work (both in terms of volume and quality) as well as the lead time of the Documentation department
  • Measure and Monitor Execution: Consistently measure and monitor departmental quality key performance indicators
  • Ensure that SOP´s are developed according cGXP guidelines and Global requirements
  • Collaborate with internal teams during inspection and provide timely and thorough support

Qualifications

  • MBO+ with several years of experience in a quality position in the pharmaceutical industry
  • Experience with pharmaceutical processes, techniques, and cGXP
  • Knowledge of relevant regulatory guidance’s
  • An eye for continuous process improvement/ efficiency
  • Clear communication skills to maintain relationships with other functions
  • Proactive and results oriented approach
  • Solution focus and the ability to make decisions
  • Fluency in English written and spoken

Function

Quality

Sub Function

Manufacturing Quality Assurance

Reports To

In process of validation

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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.