Advanced Therapy Medicinal Products (ATMP) Quality Manager (m/f/d)

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Ansprechpartner
Nadja Küppers
+49 (0)89 7263 210 – 09
kueppers@ageneo.de
Branche
Pharmazeutische Industrie
Berufsfeld
QM
Region
Southern Germany (Baden-Wurttemberg)

DAS UNTERNEHMEN

Our client a leading, international biopharmaceutical company with site in southern Germany (Baden-Württemberg) is looking for an ATMP Quality Manager (m/f/d).

IHRE AUFGABEN

Would you like to become part of an expert group, which explores new biopharmaceutical modalities / Advanced Therapy Medicinal Products (ATMP) and extends our client's manufacturing expertise within the Biopharma Contract Manufacturing Business Unit?

Then show us your strong understanding of existing and leading-edge analytical test methods and quality assurance systems in manufacturing of virus-based therapeutics.
Take your chance and provide your expertise as key input for operational and strategic decisions regarding future business cases in the field of Advanced Therapies.
 

Tasks & responsibilities

- Provide expertise and guidance to internal functions as well as to external clients in the broad range of quality test methods for viral vectors and therapeutic viruses
- Implement robust CMC compliance programs covering all aspects of the manufacturing processes, analytical test methods, specifications and shelf life maintenance
- support technical based discussions during scientific advice with regulatory agencies, i.e. EMA and FDA.
- drive interactions on quality management processes and lead the technical teams in all quality relevant topics with  industrial customer clients in development and manufacturing
- give guidance in preparing and submitting variations and market authorisation applications at different regulatory authorities, i.e. EMA or FDA
- attend and present at conferences

IHR PROFIL

- Masters/Diploma degree or Doctoral degree (PhD) in virology/biologics, biotechnology, pharmacy, or equivalent
- Career changers e.g. from the animal health sector are welcome
- Minimum 3 years of professional experience in the field of ATMPs/new biopharmaceutical modalities, preferably in analytical development of cells or viruses for new therapies
- Demonstrated expertise in quality control and/or quality systems required for the manufacturing of viral vectors and therapeutic viruses based therapeutics
- In-depth knowledge in the analytical characterization of ATMPs in the areas of drug substance and drug product manufacturing
- Expert knowledge in CMC compliance and biopharmaceutical regulations
- Proven leadership Expertise
- Good managerial and social competence (matrix leadership), such as highly developed skills in communication, conflict management coupled with assertiveness
- Bilingual: Fluent in English and one other language. The prerequisite to learn German must be given, preferably already existing basic Knowledge

BENEFITS

- The chance to build a complete new area in a well known company
- Career development opportunities through internal and external training opportunities
- Healthy and balanced meals in the staff restaurants
- Attractive salary