Manager* AS&T Lifecycle Management

  • Mainz
  • Work experience
  • Production, manufacturing
  • Quality Management, Quality Assurance
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Become a member of the BioNTech Family!

As a part of our team of more than 2.500 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.
 
We aim to reduce the suffering of people with life-changing therapies by harnessing the potential of the immune system to develop novel therapies against cancer and infectious diseases. While doing so, we are guided by our three company values: united, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives.

Manager* AS&T Lifecycle Management

As Manager* AS&T Lifecycle Management you will be responsible to provide expert knowledge to support internal and external sites on method harmonization and improvement. Further you will act as analytical expert to support transfer, validation as well as method life cycle activities (e.g. controls, standards and references).
 
Your main responsibilities are:
  • Harmonization and improvement to robustness of current analytical methods
  • Liaise regularly and effectively with Manufacturing Science and Technology team and maintain state-of-the-art knowledge in e.g. CCIT, leachables & extractables
  • Interface with external labs and CMOs as well as internal development units and communicate effectively on topics including method transfer, material request, and documentation in regards to analytical questions
  • Provide analytical guidance to site and direction on laboratory investigations, manufacturing deviations, and where required customer complaint investigations requiring analytical support
  • Provide guidance to site and direction on laboratory investigations, manufacturing deviations, and where required customer complaint investigations requiring analytical support
  • Management and coordination of references/controls/standards through the QC network (initial supply, maintenance, distribution and re-supply within the network)

What you have to offer.

We are looking for an enthusiastic, committed, and visionary individual, ideally with the following characteristics:
  • University degree in a scientific discipline (e.g. Biochemistry, Chemistry, Microbiology, Biotechnology)
  • Several years of practical experience within biotech or pharmaceutical industry in GMP regulated environment
  • Expertise in supporting transfer, validation as well as method life cycle activities (e.g. controls, standards and references)
  • High team spirit and excellent collaborating skills
  • Conscientiousness and detail-orientation
  • Creativity and the ability to develop a flexible approach to changing conditions
  • Refined colloquial and correspondence skills in both German and English

Benefits for you.

  • Company Pension Scheme
  • Childcare
  • Jobticket
  • Company Bike
  • Leave Account
  • Fitness Courses
  • Mobile Office
  • Special Vacation
... and much more.

Have we kindled your pioneering spirit?

Then apply now for our location  and simply send us your application documents using our online form.

If you have any further questions, our Talent Acquisition Team will be happy to answer them on + 49 (0) 6131-9084-1291 (monday-friday, from 12 noon to 4 pm).

Job-ID 3529 (please indicate for inquiries)

We look forward to your application!


*BioNTech does not differentiate on the basis of gender, race or ethnicity, religion, color, sexual orientation or identity, disability, age and other protected statuses as given by applicable law. We are committed to creating a diverse environment and are proud to be an equal opportunity employer. Most important – it’s a match!

BioNTech - As unique as you

https://biontech.de