Share this Job

Head (m/f/d) of Biopharmaceutical Drug Product Management

Date: Jun 4, 2021

Location: Ulm, DE, 89079

Company: Teva Pharmaceuticals

Who are we

We want to improve the life of our patients. That is our daily mission. We are proud of our 2,500 employees who provide millions of people with essential medicines every day. And that's not all: we are represented in over 80 countries worldwide, the market leader in generics, the home of Germany's well-known pharmaceutical brand ratiopharm and a leading manufacturer of biopharmaceuticals. In total, we offer a wide range of approximately 700 products. These includes innovative drugs, Biopharmaceuticals, generics and over-the-counter medicines.

In a nutshell: We are Teva - and we are very proud of it!

If you feel like us and if you are someone who enjoys exploring unknown paths - then we would like to get to know you. Are you also enthusiastic about global markets and technologies? And would you like to develop the future of healthcare at a leading provider of generics and biopharmaceuticals? Fantastic! Then become part of our team!

Curious?  Fantastic,  then  take  a  look:  https://www.youtube.com/embed/73i_f4kpfVU? rel=0&showinfo

A day in the Biologics CMO Quality

The Biologics CMO Operations and global MS&T team we are operating within Teva Biological Operations group producing and supplying Teva biological products to our patients around the globe. Our team oversees manufacturing and supply of Drug substance and Drug Product produced in multiple Teva facilities and external suppliers. Our top priority is to secure smooth supply, uncompromised quality and maximal efficiency of Teva biologics supply chain. For that matter we closely collaborated with various inter and intra company stakeholder in a dynamic international environment.

As the Head of Biologics Drug Product management you will be responsible for all technological aspects related to aseptic manufacturing of Biologics conducted in Teva's site or at various contractors' sites. You will take part in our Annual and Long term working planning, participate in our annual manufacturing plan and will lead the technological investigation and CAPAs implementation following process deviations, OOS results and change controls. You will also serve as the SME (Specific Matter Expert) for Bio Drug Product manufacturing and will support our internal sites and contractors. Occasionally you will contribute to new opportunities assessment, may participate in Due Diligence or audits and expected to lead Drug Product manufacturing excellence.

Who are we looking for

You are...
… experienced in the pharmaceutical and/or biotech industry, especially with regard to Drug Product manufacturing and related operations in a GMP regulated environment
… self-motivated and independent, with decision making capabilities
… a fast learner with the competence to solve problems and a desire to share your knowledge
... a team player with ability to work independently when needed
… a person with strong inter-personal and professional skills to interact and build relationships with internal and external parties.
… proficient with written and spoke English, German would be an asset
... familiar with Trackwise, SAP20 and Sharepoint
… willing to travel around 30% of your working time


Do you have...
… an University Degree in Biology, Biotechnology, Chemistry, Pharmaceutical Science (ideally PhD or master degree). Equivalent formal degrees may be considered in case of highly experienced candidates
… significant experience in the pharmaceutical industry, especially in development and/or production of aseptic drug product, preferred of biopharmaceutical origin
… profound knowledge and hands-on experience in formulation processes, aseptic filling, labelling and packaging with regard to sterile drug product
… considerable experienced in regulatory and quality relevant (GMP) environment with regard to deviation management, change control management and submission documentation
… sound knowledge in international regulations and guidelines (EU / FDA cGMP regulations, ICH etc.)
… experience within Third Party Quality Management is appreciated
… excellent interpersonal relationship skills, experience with multiple culture, and matrix  environments

At Teva…

… we take care of your health (among other things through a company health management system, a company doctor, physiotherapy, sports activities and a company canteen).
... you have time for your family (through our own company kindergarten and holiday camps for school children, as well as 30 days of vacation).
... you can develop your potential to the fullest (through a comprehensive virtual training program). ... your achievements are valued accordingly (e.g. through recognition and Senior-LeadersPrograms, as well as various company events).
... we think together with you about your future (e.g. through a company pension scheme).


Project Management

Reports To

VP Bio CMO Operations and MS&T

Contact Person

Julita Mlynska
Talent Acquisition

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.