Senior Quality Systems Associate

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 Quality Systems Associate supports the site's Quality Systems & Compliance team in establishing and maintaining quality at the department in accordance with Site SOP’s, Teva Global Standards, regulatory guidelines and cGXP compliance requirements.

 

Responsibilities

 

• Maintain high standards of quality at the department through managing and continuously improving the effectiveness of the department quality processes and systems
• Consistently measure, monitor and report site quality key performance indicators
• Support in identifying, developing, and retain qualified people to implement the quality processes
• Participate in team’s that have the technical expertise, personal skills and interpersonal skills needed to influence site Operations and is conversant in application of regulations
• Maintain a culture of enhancing quality throughout the entire site operation, ensure an effective internal communications structure with relevant departments
• Risk based quality decision making. Review and provide options to meet business needs without compromising quality and compliance
• Share best practices, challenges and lessons learned at the site and on SME topics also across the Teva Quality organization in order to improve the performance of quality globally
• Ensure product transfers across sites also include the transfer of quality information (knowledge, risks, documentation for manufacture and control processes, validations, Product Quality Reviews)
• Timely management of investigations, CAPAs, coordination of Regulatory commitment, GRAs, Audits, standard implementation to ensure sustainable compliance

 

 

 

Qualifications

 

• Degree in science (Pharmacy / Chemistry) or HBO with several years of experience in a quality position in the pharmaceutical industry
• Experience with pharmaceutical processes, techniques, cGXP and process automation
• Ability to communicate technical, regulatory and business issues in a clear (and when necessary, in a non-technical) way
• Ability to understand and define a problem clearly
• Clear and timely Decision-making skills
• An eye for continuous process improvement/ efficiency
• Fluency in English written and spoken

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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.