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Mantell Associates is partnered with a global CDMO in their search for an experienced Associate Director of Operations – Immunochemistry to lead operational activities in the Netherlands. This is a strong opportunity to join a growing global CDMO and play a key leadership role in advancing bioanalytical capabilities while supporting the development of innovative therapies.
Job Responsibility:
Provide operational leadership for the immunochemistry department, ensuring efficient execution of bioanalytical studies and laboratory workflows
Translate strategic objectives into operational plans, managing capacity, resources, and project prioritization
Oversee laboratory performance, including planning of study activities, resource allocation, and delivery timelines
Ensure compliance with GLP/GCP standards and global regulatory expectations, maintaining strong audit and inspection readiness
Support quality systems activities including deviations, CAPAs, audit findings, and continuous improvement initiatives
Drive operational efficiency by optimizing laboratory processes, workflows, and performance metrics
Collaborate with cross-functional teams including Quality, Project Management, and Scientific Leadership to ensure successful study delivery
Provide operational input into new project proposals and support client interactions when required
Lead, mentor, and develop scientific and operational staff within the immunochemistry team
Contribute to long-term operational planning, technology evaluation, and capability development
Requirements:
MSc or PhD in Biochemistry, Analytical Chemistry, Pharmacology, or a related Life Sciences discipline
Significant experience working within bioanalytical laboratories or biopharmaceutical service environments
Strong expertise in immunochemistry or immunoassay platforms, including biomarker or immunogenicity assays
Proven leadership experience managing scientific teams and operational workflows in regulated environments
Strong understanding of GLP/GCP regulatory requirements and audit/inspection readiness
Demonstrated ability to manage complex study portfolios and drive operational improvements
Excellent communication and leadership skills with the ability to engage both internal teams and external clients
Ability to work within a fast-paced CDMO environment supporting global pharmaceutical partners