IMP Quality Manager

Proclinical Staffing; Schweiz; Vor Ort; CHF 80’000 - 120’000; Vollzeit

Zusammenfassung

Une entreprise leader dans le recrutement de sciences de la vie recherche un Quality Manager pour garantir des normes de qualité dans la production de médicaments investigateurs. Le candidat idéal possède une formation en sciences de la vie, une expérience en GMP, ainsi que des compétences en communication en anglais et allemand. Ce rôle implique une collaboration étroite avec les unités de production et les équipes d'emballage clinique, ainsi qu'une forte autonomie et un bon sens du détail.

Qualifikationen

• Expérience dans l'industrie pharmaceutique et environnements GMP.
• Connaissance des exigences qualité pour le développement clinique.
• Proficient en communication en anglais et allemand.

Aufgaben

• Agir en tant que représentant de l'assurance qualité dans la production de médicaments investigateurs.
• Assurer la conformité avec les normes GMP pour les processus de fabrication et de test.
• Conduire des inspections dans les usines de fabrication et les laboratoires.

Kenntnisse

Communication

Flexibilité

Résolution de problèmes

Ausbildung

Diplôme en Sciences de la Vie ou domaine connexe

Jobbeschreibung

Are you passionate about quality and precision? Join our client as a dedicated Quality Manager and help ensure top-tier standards every day.

Proclinical is seeking an IMP Quality Manager to ensure that all investigational medicinal products meet quality standards and comply with regulations. You will work closely with manufacturing units and clinical packaging teams to maintain high-quality operations. This position requires flexibility, strong communication skills, and a deep understanding of Good Manufacturing Practices (GMP).

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Act as a representative for quality assurance in the production of investigational medicines.
• Ensure compliance with GMP standards for manufacturing and testing processes.
• Review and approve quality procedures and reports.
• Conduct inspections in manufacturing plants and labs.
• Report directly to the quality assurance leadership team.

Key Skills and Requirements:

• Degree in Life Sciences or a related field.
• Experience in the pharmaceutical industry and GMP environments.
• Familiarity with manufacturing and quality control of sterile products.
• Strong knowledge of GMP and quality requirements for clinical development.
• Proficient in English and German communication.
• Ability to work independently and collaboratively, with strong problem-solving skills.
  

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at [e-mail].

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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