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!
As Senior Director Scientific Affairs you will be responsible for project management of pre-commercial activities within Medis. Your scope includes regulatory support for International and EU markets and ensuring the needs of the cluster are met through technical expertise and providing project management between customer, Global Regulatory Affairs (GRA), Supply Chain (SC) and site technical functions.
Providing expert technical guidance and support to the Supply Chain team to ensure tech transfer and site transfer are on time, whilst supporting Customer Experience and Business Development (BD) teams to provide support regarding technical questions from customers
Providing support to customers directly and be actively involved in pre-commercial discussions with BD on technical aspects as needed
Responsible for working with Clusters and customer to develop regulatory strategy, taking into consideration the various requirements especially in International Markets to support LRP (long range plan) and AOP (annual operating plan)
Support technically on registration strategy within Medis; provide regulatory guidance /support to the International Market (IM) Cluster
Act as a liaison to Teva GRA and other relevant units to support the commercial needs of Medis
Coordinating communication between Medis and key contacts within Teva, in R&D, global RA, site RA and other functions as relevant to ensure timely response to deficiency letters from health authorities to Medis clients in IM markets
Providing overall technical expertise to support BD activities
Responsible for carrying out your tasks diligently and for any additional specific tasks/projects as assigned by the Head of Medis
MSc/PhD required, preferably in pharmacy of life sciences
+10 years of experience in regulatory affairs or clinical development is required
Understanding of pharmaceuticals from a technical perspective is a must
Project management skills/experience paired with excellent organisational skills
Strong leadership skills and good team player
Strategic thinking and flexibility to adapt to changes
Proactive way of working and able to work independently
Excellent communication and presentation skills
Written and verbal proficiency in English language
Good computer stills (MS Office)
Sales SupportTevas 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.