Ruben Wohlfarth

Senior Process Technologist Parenteral Launch & Innovation

Ingelheim am Rhein, Rhineland-Palatinate, Germany

About

Experience

  • Senior Process Technologist - Launch & Innovation at Boehringer Ingelheim
    Apr 2025 - Present · 1 yr 3 mos

  • Bayer (Full-time · 5 yrs 1 mo)
    • Quality Specialist - Market Supply
      Feb 2024 - Mar 2025 · 1 yr 2 mos

    • Short Term Assignment - DP Formulation Development
      Aug 2023 - Jan 2024 · 6 mos

    • Quality Specialist - Clinical Supply
      Mar 2020 - Jul 2023 · 3 yrs 5 mos

  • Licensed Pharmacist at Premium Apotheken Berlin
    Sep 2019 - Mar 2020 · 7 mos

    - Ensuring the proper supply of medications and medical devices to patients, as well as providing pharmaceutical services - Improving and monitoring the pharmacy's Quality Management System (QMS) - Continuously enhancing medication therapy safety for patients by identifying contraindications, risks of misuse, and long-term use - Providing information and counseling to other healthcare professionals - Practical training of pharmacy interns according to §4 of the German Pharmacy Licensing Regulations (AAppO)

  • Pharmaceutical Intern at Premium Apotheken Berlin
    Dec 2018 - May 2019 · 6 mos

    Training in the following areas: - Fundamental principles of compounding and small-scale manufacturing - Providing information and counseling to patients, physicians, and other healthcare professionals on medications and medical devices, particularly regarding proper storage, application, incompatibilities, drug interactions and risks of long-term use and misuse of medications - Communication techniques for interacting with healthy individuals, patients and their relatives, physicians, and other healthcare professionals - Aspects of quality assurance and quality control

  • Pharmaceutical Intern at Bayer
    Jun 2018 - Nov 2018 · 6 mos

    Gained insights into the production of parenteral drugs, including: - Working in different cleanroom classes within a GMP-compliant environment - Filling of terminally sterilized and aseptically filled parenteral products - Sterilization processes - Microbiological and chemical process control - Preparation, coordination, and execution of validation plans and reports - Deviation management - Supporting the response to regulatory inquiries - Analyzing process-relevant data for discussion with international expert groups