Responsible for developing and implementing a global genetics lab footprint strategy, including facility planning, CAPEX management, and lab engineering projects. Drives standardization, automation, regulatory compliance (ISO 15189, ISO 17025, CE‑IVDR), and cross-functional collaboration to optimize lab performance and cost-efficiency.
Responsibilities
Support the development and implementation of a global lab footprint strategy to optimize the distribution of genetics laboratories and testing sites across regions.
Identify and support consolidation, expansion, and relocation opportunities to improve efficiency and service delivery.
Support CAPEX planning and execution for laboratory infrastructure projects, ensuring alignment with business growth and regulatory requirements.
Support the standardization of laboratory processes across all regions to enhance operational performance and cost efficiency.
Support the design, construction, and maintenance of state-of-the-art laboratories to enable evolving diagnostic capabilities.
Ensure compliance with industry standards for laboratory design and operations (ISO 15189, ISO 17025, GMP, etc.).
Ensure compliance with CE-IVDR regulations.
Implement automation and digitalization in laboratory processes to improve efficiency and accuracy.
Collaborate with IT and Digital teams to integrate Laboratory Information Management Systems (LIMS) and other smart lab technologies.
Apply Lean and Six Sigma principles to improve productivity, reduce waste, and enhance turnaround times.
Benchmark and develop operational KPIs across laboratories to identify opportunities for continuous improvement and standardization.
Advise on optimization of resource utilization to reduce operational costs without compromising quality and compliance.
Support and actively participate in modeling and adapting Genetics Target Operating Models at lab, country, and international network levels, working with cross-functional teams.
Act as the project liaison between the 3L team and medical, group, and country stakeholders.
Requirements
Bachelor’s degree in Engineering, Supply Chain, Biomedical Sciences, or a related field.
Master’s degree or PhD in Genetics required.
Minimum of 10 years’ experience in genetics laboratory operations or engineering within diagnostics, healthcare, or life sciences.
Deep knowledge of laboratory workflows, regulatory requirements, and automation technologies.
Experience in facility planning, CAPEX investments, and laboratory engineering projects.
Proven ability to work in cross-functional and international team environments.
Strong project management skills.
Knowledge of Lean, Six Sigma, and continuous process improvement methodologies.
Familiarity with LIMS (Laboratory Information Management Systems) and automation trends in laboratory operations.
Excellent communication skills.
Location: UK or Germany.
Languages: Fluent in English. German and/or Italian desirable.
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