Your responsibilities include:

Development and optimization of formulations and manufacturing processes for solid oral dosage forms, as well as transfer to production scale and participation in process validation.
Handling complex technological issues and advising customers during the acquisition phase
Creation of the development concept for the customer offer
Creation of experimental design and technical coordination of development trials and clinical sample production, evaluation of results and analytical data, and presentation of these to customers or internal stakeholders.
Coordination and participation in the creation of GMP-relevant documents within the context of drug manufacturing
Taking over and managing (sub-)projects as well as providing technical support and coordination of sub-projects within a project team

Your applicant profile:

You have successfully completed a degree in pharmacy, process engineering or a comparable scientific discipline and ideally hold a doctorate in pharmaceutical technology.
You bring professional experience in pharmaceutical development and manufacturing and possess extensive expertise in the development and manufacture of solid dosage forms (desirable).
They have very good German and English skills, both spoken and written.
They enjoy working with others, approach challenges in a solution-oriented manner, and act with an entrepreneurial mindset.
With openness and self-reflection, you and your environment will continuously develop further.

How To Apply:

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Responsibilities

Development and optimization of formulations and manufacturing processes for solid oral dosage forms, as well as transfer to production scale and participation in process validation.
Handling complex technological issues and advising customers during the acquisition phase
Creation of the development concept for the customer offer
Creation of experimental design and technical coordination of development trials and clinical sample production, evaluation of results and analytical data, and presentation of these to customers or internal stakeholders.
Coordination and participation in the creation of GMP-relevant documents within the context of drug manufacturing
Taking over and managing (sub-)projects as well as providing technical support and coordination of sub-projects within a project team

You have successfully completed a degree in pharmacy, process engineering or a comparable scientific discipline and ideally hold a doctorate in pharmaceutical technology.
You bring professional experience in pharmaceutical development and manufacturing and possess extensive expertise in the development and manufacture of solid dosage forms (desirable).
They have very good German and English skills, both spoken and written.
They enjoy working with others, approach challenges in a solution-oriented manner, and act with an entrepreneurial mindset.
With openness and self-reflection, you and your environment will continuously develop further.