Laboratory Manager Pathology CAP/CLIA (m/f/d)

Das ist der Job

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Darum lohnt es sich

Key Responsibilities • Visionary Operational Leadership: Supervise the daily “rhythm” of the laboratory, synchronizing pathology and immunoassay workflows to ensure competitive turnaround times. • Guardian of Quality: Maintain an “inspection‑ready” culture, serving as the primary lead for CAP/CLIA and ISO 15189 audits. • Champion of People: Lead, mentor, and inspire a team of laboratory scientists, fostering a culture of continuous learning and technical excellence. • Strategic Technical Oversight: Manage the validation and implementation of new assays and novel platforms, ensuring every piece of equipment is a high‑performing component of the diagnostic system. • Innovate & Improve: Actively identify opportunities for workflow optimization and cost‑effective management without compromising the quality that defines the Roche name.

Laboratory Manager Pathology CAP/CLIA (m/f/d) • Biologe/Biologin The Position Oversee a dual‑specialty pathology and immunoassay laboratory, ensuring operational excellence across the Histology/Pathology and Immunoassay/Chemistry departments, while maintaining compliance with ISO15189, CAP, and CLIA regulations.

The Opportunity Lead a dual‑specialty laboratory at the forefront of the industry, overseeing two critical domains. • Anatomic Pathology: Managing high‑complexity tissue‑based diagnostics, including advanced Immunohistochemistry (IHC) and In Situ Hybridization (ISH). • Immunoassay Excellence: Driving peaks of operational efficiency on state‑of‑the‑art cobas® platforms.

Qualifications • Hold a Bachelor’s degree in Clinical Laboratory Science, Medical Technology, or a related Biological Science; a Master’s (MHA/MBA) or PhD highly preferred. • 5+ years of experience in a clinical laboratory setting. • Proven expertise in both anatomic pathology and automated immunoassay workflows. • At least 2 years of experience in a leadership role, fostering a culture of quality, safety, and continuous improvement. • Track record of zero‑deficiency inspections and passion for navigating the complexities of emerging global regulations.

References and certificates are not required at this stage. Please apply with English application documents.