Your Role:
Siegfried DINAMIQS is a Contract Development and Manufacturing Organization (CDMO) based in Schlieren-Zurich, Switzerland, specializing in the manufacturing of viral vector gene therapies. At DINAMIQS we offer a comprehensive range of services, including vector design optimization, cutting‑edge process development and analytics, as well as manufacturing. With an R&D facility running since 2022 and a newly constructed GMP facility, we are dedicated to supporting gene therapy projects with scalable and efficient solutions.
Implementing quality systems and planning QA‑related workflows to support the GMP facility
Actively involved in aseptic manufacturing and environmental monitoring processes
Act as the primary QA contact in the GMP facility including on the shop floor
Review and approve batch records, deviation reports, and other quality documents
Conduct root cause analysis and manage CAPA processes
Actively contribute to a culture of quality and continuous improvement throughout the organization
Your Profile:
M.Sc. or PhD in Biotechnology, Virology, Molecular Biology or related fields.
At least 5 years of experience in a GMP‑regulated biopharmaceutical environment.
In‑depth knowledge of viral vector production processes and related quality control techniques is desired.
Strong understanding of regulatory requirements (e.g., EMA, FDA) and industry guidelines (GMP).
Experience in aseptic manufacturing (Annex 1) preferred.
Excellent analytical and problem‑solving skills.
Exceptional communication and interpersonal skills.
Proficiency with QMS software and quality management tools.
Fluency in English, German would be a plus.
Your Benefits:
A unique and amazing work experience, being part of one of the most dynamic, diverse and inclusive CDMOs in the industry
Competitive and attractive compensation
5 weeks holidays and flexible working hours make it possible to combine family, leisure time and career
Impactful Work: Make a significant difference through innovative gene therapy projects
Learning Opportunities: Develop diverse skills in a dynamic environment
Fast‑Paced Environment: See results quickly and enjoy creative freedom in defining your operating model and go to market strategy
Are you interested in joining a motivated team with an inclusive and collaborative culture? Then take the next step and send us your application.
Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know‑how and experience makes us the most trusted partner in the pharmaceutical industry.
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