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!
Working at Teva is more than a job - our people get to make a meaningful impact on the lives of thousands of people every day. We manufacture a broad portfolio of life-saving and medically necessary pharmaceuticals that are used by patients who have cancer or who suffer from lung diseases. As a leading producer of these and other generic medicines, we play an important role in safeguarding access to medicine across the world.
Do you want to be part of our journey?
As Regulatory Affairs Assistant you will support and assist in variable regulatory activities provided by the Finnish Regulatory Affairs team members. You will be updating Product Information texts for medical and non-medical products, which will be send to the authorities. Next to that you can be assigned to tasks related to packaging materials, such as requesting artwork, checking and approving them accordingly.
Who are you?
You are a motivated pharmacy or similar life science student that has already 1 year of studies experience that wants to learn more about the Regulatory Affairs duties and responsibilities in a Finnish affiliate of a Global Pharmaceutical company.
Next to your education you have English, Finnish and Swedish language skills.
On top of all this; we believe that you are an accurate with good organizational skills and a good team player with an enthusiastic and positive attitude.
We are offering a temporary Regulatory Affairs position full time for the summer months (May-August) 2025.
a nice team that supports you flexible working hours and hybrid working (office in Keilaranta) lots of learning opportunities international working environment company culture that supports sense of community
The last possible date to apply is April 1rst 2025.
Job Responsibilities Regulatory AffairsReports To
Assoc Dir Regulatory Affairs
Contact
Judith Horn
Recruiter
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 applyy: 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.