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! Your tasks
Within this position you will secure internal and external Bio DP development and commercial manufacturing (contractual obligations of the respective CMOs with regard to the supply and quality agreements)
You will act as single point of contact for the respective CMOs and internal stakeholders (R&D, QA, DP manufacturing Sites) with regards to the relevant products during development and commercial manufacturing
You will be responsible for end-to-end management of Bio DP development and commercial manufacturing
You will be responsible for the development, evaluation, implementation and validation of the drug product manufacturing processes at the respective CMOs (incl.
e.g. formulation, aseptic filling, labelling and packaging)
You will provide technical support, trouble shooting, investigation and knowledge sharing with regard to Bio DP commercial manufacturing
You will be in charge of CMO development and actively contribute to internal DP development and commercial site allocation
You will be in charge for and Bio DP CoGs monitoring and optimization
You will be responsible for supervision of deviation management, change control management and process optimization during development and production
You will coordinate documents for regulatory submissions (CMC part) and the annual reports
You will contribute during preparation of development and production agreements with regard to commercial and quality aspects
You have (Bio) Pharmaceutical education (PhD or master degree)
You gathered significant experience in the pharmaceutical industry, especially in development and / or production of aseptic drug product, preferred of biopharmaceutical origin
You have profound knowledge in formulation processes, aseptic filling, labelling and packaging with regard to sterile drug product
You are well experienced in regulatory and quality relevant (GMP) environment with regard to deviation management, change control management and submission documentation
You have great interpersonal relationship skills, experience with multiple culture environments as well as matrix structures
You self-motivated are independent, with decision making capabilities
You are willing to travel around 30%of your working time
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.