Site Quality Head - TAPI

Who We Are

TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service.

Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market.

The opportunity

Join our mission in TAPI: Advancing health from the core.

TAPI will soon continue as a standalone organization, fully dedicated to API & CDMO services. Join us on our standalone journey!

Are you ready to make a significant impact on our company's future? We are seeking a Site Quality Head to lead our quality assurance and control efforts at our production site in Malanpur, India. In this pivotal role, you'll be the architect of our quality management framework, ensuring we maintain the highest standards in production and product excellence.

As the leader of our site quality function, you'll collaborate closely with our production and operations teams to create a seamless and consistent experience for our customers. Your influence will extend beyond strategy; you'll be a key player in nurturing growth within our quality community. Additionally, we need someone who can roll up their sleeves and be a hands-on quality partner for our site teams, bringing your expertise directly to the heart of our operations. You'll also be responsible for designing and implementing quality systems, driving continuous improvement and high performance across our organization.

Join us and be a driving force in shaping a future of excellence for our team!

How You'll Spend Your Day

• Lead the Quality organization, including Quality Control, Microbiology, Compliance, Systems, and Assurance Operations
• Ensure and continuously improve the Quality Management System
• Guarantee products meet cGMP requirements and registered specifications
• Serve as the senior authority on product quality and market actions
• Identify and mitigate quality risks to ensure product safety and effectiveness
• Collaborate with Site GM and Global Quality to design and implement the site quality program
• Oversee quality data management and delivery to stakeholders
• Direct laboratory activities, including testing and approval of materials
• Foster a culture of quality and encourage open communication and innovation
• Maintain strong partnerships with the site leadership team
• Act as a strategic partner to ensure project timelines and objectives are met
• Provide leadership during inspections by internal, customer, and Health Authorities
• Ensure Quality KPIs meet targets and monitor CAPA commitments
• Manage the annual Quality Operations budget and resources
• Assist the Head of Quality function TAPI and approve related documents
• Perform additional responsibilities as assigned by the Head of Quality function TAPI
• Reporting to the VP Quality directly and incumbent will be part of site leadership team under the lead of the General Manager
  
  

Your Experience And Qualifications

• The ideal candidate will possess a degree in Chemistry, Science, Chemical Engineering, or a related scientific field
• They should have over 10 years of experience in the pharmaceutical or API production industry, specifically in India
• Proven experience in leading a Site Quality Head role
• The candidate must have extensive experience in preparing for and managing inspections and audits from global authorities such as the FDA, local and European authorities, and Japanese regulatory bodies
• They should have in-depth knowledge and hands-on experience in deviation management, Corrective and Preventive Actions (CAPA), quality systems, and handling complaints
• Additionally, a solid background in Quality Control processes and practices is required
• The ideal candidate is an experienced leader with a proven track record of managing teams
• You will be responsible for leading Quality Assurance (QA), Quality Control (QC), and Quality Systems (QS) teams
• You possess excellent communication skills, capable of conveying complex ideas clearly and effectively
• You have the ability to build strong relationships and foster collaboration across teams
• You are passionate about inspiring and motivating team members to achieve their best
• You are comfortable making decisions under pressure, with a strong sense of integrity
• You demonstrate empathy and understanding, creating a supportive and inclusive work environment
  
  

Reports To

Direct reporting line to Head of Quality with a dotted line to the Site General Manager

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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.