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Site Quality Director

Date: Dec 22, 2021

Location: Santiago, CL, 9250000

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

 

Job title: Site Quality Director

 

Purpose: Provides strategic leadership working closely with Site Head to achieve the corporate and strategic goals to support clinical and commercial manufacturing, continuous improvement and maintain inspection readiness state of the facility. This role will maximize value, impact and delivery in assuring compliance, excellence in quality and readiness for future needs.

 

Experience: 5 years in similar positions for pharmaceutical industries. Assuring quality of company´s products, complying with current Regulations and with assigned budget. To manage and organize the area activities, assuring the strategic company´s plan. Analyze and investigate corrective actions responding to ISP requirements. Manage assigned resources for the area. 

 

Key Responsibilities:

1. To work closely with business stakeholders from Manufacturing and Supply chain as well as Internal Quality functions to deliver quality outcomes and operational excellence. Will be part of the quality leadership team and will participate in management review.

2. This position will report to Regional Quality Sr Director and will work closely with different stakeholders supporting product development and commercialization. Will demonstrate Company’s values as well as model leadership, instilling a culture of quality engagement, development and transparency.

3. To be responsible for setting goals, Budget and monitoring people development to establish a strong team.

Qualifications

 

Academic Background: Bachelor´s Degree as Chemical Pharmaceutical, Chemical Engineer, or related that has experience at the local and international legislations and pharmaceutical industries.

Language: Advanced English

Function

Quality

Sub Function

Quality Assurance Methods

Reports To

Sr. Director Latam Quality Head

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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.