Job Information
Teva Pharmaceuticals Associate Director Distribution & Commercial Quality - TAPI in Amsterdam, Netherlands
Associate Director Distribution & Commercial Quality - TAPI
Date: Sep 18, 2024
Location:
Amsterdam, Netherlands, 1019
Company: Teva Pharmaceuticals
Job Id: 58345
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.
Location of the position
This position is located in Amsterdam (NL) or near out production locations in Italy, Croatia, Hungary or Czechia.
The opportunity
The person holding this role will support the Global Distribution, Logistics and Commercial Supply Chain to ensure that the distribution and logistics department i.e. transportation, warehousing and storage, function in a way that is in accordance with Good Distribution Practices (GDP) , Good Warehousing and storage Practices ( GWP/GSP) and Good Manufacturing Practices (GMP). This role should ensure that all products manufactured by TAPI are transported, stored and delivered to TAPI’s customers in the most efficient and compliant way without negatively affecting the quality of the product. The person holding this role will be responsible for managing the commercial QA team in Japan and EU and all other work processes of quality management and compliance for distribution centres in accordance with GDP guidelines and TAPI QMS requirements. The person will also be responsible for cGMP compliance by supporting TAPI sites in the network with respect to transportation and warehousing vis-a-vis inspection readiness, execution and follow up of audits, investigations, risk assessments and maintaining the TAPI Quality Management System.
How you’ll spend your day
Create and maintain Good Distribution Practice (GDP) related TAPI policies, SOPs and guidelines.
Support and drive Logistics development of QMS as part of continuous process improvement.
Manage logistics service providers and provide support in the quality guidance and GDP development of same together with any relevant training from a quality logistics perspective.
Prepare shipping qualifications protocols and reports.
Qualify transportation providers and their maintenance.
Qualification of transportation containers, logistics flow and warehousing and storage providers.
Collaborate with relevant regional managers in areas of responsibilities arising from the matrix structure on KPIs and reports for the whole region.
Perform periodic irregularity reporting and trending, develop annual report on temperature excursions in transportation for the region.
Perform operational investigation, evaluate and approve CAPA plans for transport and logistics related irregularities
Provide inspection readiness support to sites related to logistics issues, before, during and after Health Authority inspections.
Ensure that logistics processes are in compliance with GDP and GMP as applicable to respective country agency regulations and requirements.
Your experience and qualifications
Bachelor's or Master’s Degree in Supply Chain Management, or Logistics or Distribution preferably related to the supply of Pharmaceutical products.
Minimum of 10 years of experience as a functional leader in Distribution/Commercial Quality function is a must with technical, team management, and operational responsibility in a pharmaceutical company.
Advanced practical knowledge of supply chain management of pharmaceuticals*.
Adequate knowledge of local current and upcoming legislation and current Quality best practices*. International experience is an advantage.
Advanced knowledge of cGMP and GDP requirements for products and process*.
Advanced understanding and insight into the different aspects of quality functions related to QA, Quality Systems, Compliance, Documentation, etc.*.
Adequate knowledge of MRP Systems and GMP impacting computer systems, like SAP, LIMS and software platforms typically used by TAPI*.
Ability to understand and execute against TAPI Quality Management System*.
Adequate knowledge of logistics, distribution function and quality systems*.
Advanced experience in working within a matrix environment.
Advanced communication skills – written and verbal*
Advanced team working skills*
Must be able to travel based on business need; up to 30% when critically required (domestic and international)*
Fluent in English – a must
Reports To
Global Head of Quality Compliance -TAPI
Contact person
Vincent van Straten - Team Lead Recruitment
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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
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.
Pre Employment Screening
TAPI will carry out appropriate verification and legally permitted vetting prior to the confirmation of any offer of employment. More information on this verification and vetting will be provided if you reach this stage of the application process.
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.
EOE including disability/veteran