KI-Beschreibung

As an R&D Business Area Manager, you will lead innovative projects in mechanical surface characterization, guiding a talented team and collaborating across departments to ensure product success and market alignment.

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  At least 10 years of experience in R&D
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  Strong expertise in developing measuring instruments
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  Proven track record managing multidisciplinary teams

KI-Beschreibung

In this role, you will ensure compliance and operational excellence by managing GMP/GDP documentation, leading risk assessments, and driving continuous improvement initiatives. Your expertise will support training readiness and maintain audit preparedness in supply chain operations.

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  Minimum 5 years of experience in GMP-regulated pharmaceutical or biotech environment
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  Strong knowledge of GMP/
  GDP regulations and quality systems
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  Experience with electronic Quality Management Systems (e.g., Veeva)

KI-Beschreibung

In this role, you will focus on developing and implementing risk-based quality management strategies for clinical trials. Your day-to-day responsibilities will involve collaborating with various teams to ensure compliance, address quality issues, and enhance processes throughout the study lifecycle.

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  Minimum 8+ years QA experience or relevant experience in quality management, biomedical science, clinical development, or regulatory compliance
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  B.S. and/
  or M.S. in Chemistry, Biology, or Health or Quality related field or equivalent combination of education, training, and experience
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  Demonstrated applied knowledge of ICH/
  GCP, regulatory guidelines/
  directives, clinical research processes and principles of Quality Assurance

KI-Beschreibung

In this role, you will be actively involved in the production of pharmaceutical products, ensuring compliance with GMP standards while operating automated lines and maintaining equipment. Day-to-day tasks will include preparing mixtures, cleaning, and documenting processes, all while prioritizing safety and efficiency.

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  CFC-level education and 5 years of experience in the pharmaceutical industry or equivalent
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  Perfect mastery of French
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  Knowledge of BPF/
  GMP environment

KI-Beschreibung

As the MES IS/IT FAS Manager, you will lead a team to ensure system reliability while driving digital transformation. This role involves managing projects, developing skills, and collaborating across teams to enhance factory operations while maintaining high safety and quality standards.

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  Background in computer science, automation, or related engineering field
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  Proven experience leading MES projects
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  Strong MES operational support experience

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