Process Design Expert (m|f|d) Cell & Gene Therapy

As a Process Design Expert in the Global Supply Chain (GSC) you will design optimize and harmonize the core processes digital tools and documentation that enable the clinical and commercial supply of our cell and gene therapy products. 

You will serve as the subject matter expert for process mapping workflow optimization documentation and system requirements  ensuring scalable compliant and efficient operations in a highly regulated environment. 

• You colead the design optimization and implementation of Global Supply Chain (GSC) processes including process mapping reengineering documentation (SOPs RAs) and continuous improvement activities. 
• The translation of user and business requirements into clear specifications for workflow and work aids is also on your agenda and you will support equipment & process qualification and validation as well as implementation. 
• In addition you oversee regular alignment with QA on GSCrelated processes and documentation while supporting audits trainings and compliance activities (DEVs CEXs). 
• You contribute to the development maintenance and enhancement of digital tools and workflow systems ensuring usability compliance and scalability. 
• As an integral part of a team of process design experts you drive cross-functional alignment and continuous improvement with the Clinical Development and Commercial team GSC team QA Manufacturing and you ensure harmonized consistent compliant process execution across clinical and commercial supply chains. 

Qualifications :

• You hold a university degree in engineering life sciences supply chain/operations or a related field. 
• You bring proven experience in process design and GxP documentation (SOPs Work instructions Risk assessments) within pharma biotech or another regulated environment. Management consulting experience is a plus. 
• You have a strong operational excellence skill set (process mapping KPI definition risk-based thinking root cause analysis) with the ability to translate complex operations requirements into clear structured and auditable workflows. 
• Additionally you have hands-on experience with commercial or clinical supply chain processes (e.g. planning CMO oversight distribution and GMP quality interfaces). 
• You are an effective communicator who enjoys working with diverse stakeholders across functions and you are reliable detailoriented and work with a proactive solutionoriented mindset. 

Additional Information :

What we offer  

• Working with free and self-determined time management also mobile working 
• An intercultural environment characterized by diversity and flat hierarchies 
• Freedom to contribute creatively and play an active role in shaping the company 
• Individual further training in our Miltenyi University as the core of the Miltenyi DNA 
• 30 days of vacation discounted ticket to Germany (e)-bike leasing capital-forming benefits company pension plan disability insurance canteen and much more. 

Diversity is the bedrock of our creativity 

Our mission: To innovate treatments and technologies and tackle the worlds most serious health challenges. And thats why we connect the dots across various disciplines linking different perspectives skills and abilities. 

You and your talent are welcome here in our inclusive and collaborative environment. So come as you are. Regardless of gender sexual identity age ethnicity religion or disability. 

Become part of our team and focus on pushing the borders of medicine. 

We look forward to your application 

If you want to work in an open creative and supportive team this is the place for you. We look forward to receiving your application along with your salary expectations and availability. 

Remote Work :

No

Employment Type :

Full-time