Scientist, Research Scientist, Clinical Research

Scientist

BÜHLMANN Laboratories AG Vacant since : 10. Schönenbuch (BL) 100% By agreement Permanent

• Project Management & Phase Leadership:
  Lead development projects across feasibility, optimization, transfer, and validation phases; manage project plans, budgets, risk mitigation, and cross-departmental alignment.
• Workstream Management & Deputy Function:
  Supervise workstream contributors, coordinate multi-functional actions, and serve as deputy to the Lead Manager Gastroenterology IVD Development / Director.
• Experimental Planning & Bench Work:
  Plan, execute, and evaluate complex laboratory experiments for IVD kit development, assay optimization, and performance/stability assessments.
• Immunological Testing & Assays:
  Execute assays across multiple platforms (e.g., ELISA, PETIA, Flow Cytometry) and handle biological sample preparation (stool, blood, urine).
• Quality & Regulatory Documentation:
  Create and review critical technical documentation, including Design History Files (DHF), Device Master Records (DMR), SOPs, and risk management files.
• Data Evaluation & Biostatistics:
  Perform advanced data evaluation, apply biostatistical models, and present analytical findings to internal teams and external stakeholders.
• External Collaborations:
  Initiate and maintain scientific collaborations with external partners and clinical experts for product evaluations.
• Lab Management & Mentorship:
  Maintain instrument compliance within a GMP environment, train laboratory staff, and supervise students/interns.

• Education:
  
  Bachelor, Master of Science, or PhD degree in Biology, Chemistry, Biochemistry, Immunology, or a related field.
• Professional
  
  Experience:
  
  Proven experience in IVD product development, product validation, and design transfer processes.
• Technical & Scientific Background:
  Strong theoretical and practical foundation in immunodiagnostic techniques and diverse analytical platforms.
• Data & Biostatistics:
  Profound biostatistical skills and advanced experience with data evaluation software (e.g., Origin, R).
• Quality & Compliance:
  In-depth knowledge of IVD regulatory requirements, DHF/DMR creation, risk management, and GMP lab standards.
• Leadership &
  
  Soft Skills:
  
  Strong self-management, high precision, excellent collaboration and motivation skills, resilience, and assertive communication.
• Languages:
  
  Highly proficient in spoken and written English; conversational/basic German is a strong asset.

• A senior-level position with high visibility, project ownership, and leadership responsibility in IVD innovation.
• Close collaboration with an interdisciplinary team of experts and direct impact on international patient care.
• Dynamic, stable medium-sized business environment with modern laboratory infrastructure.

Are you ready to advance your career in gastroenterology IVD development?

• Work location 4124 Schönenbuch (BL)
• Workload 100%
• Employment start By agreement
• Employment duration Permanent

• By online Online form