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Associate Director of Operations – Immunochemistry

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Mantell Associates

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Location:
Netherlands

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Contract Type:
Not provided

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Salary:

Not provided

Job Description:

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

Additional Information:

Job Posted:
March 19, 2026

Employment Type:
Fulltime
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