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SystImmune

Associate Director / Director, Bioanalytical Laboratory

SystImmune, Washington, District of Columbia, us, 20022

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Associate Director / Director, Bioanalytical Laboratory

Associate Director / Director, Bioanalytical Laboratory

1 day ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Position Summary

SystImmune is seeking an Position Summary

SystImmune is seeking an

Associate Director or Director of Bioanalytical Laboratory

to lead U.S.-based bioanalytical functions supporting our global clinical development programs, with a particular focus on pharmacokinetics (PK) and anti-drug antibody (ADA) analysis for ADCs and other biotherapeutics.

The role, based in Redmond, WA, involves strategic leadership of laboratory operations, scientific oversight of method development and validation, regulatory compliance management, and close collaboration with cross-functional and international teams, especially in China.

This is a high-impact, hands-on leadership position requiring deep scientific expertise, regulatory knowledge, operational excellence, and strong communication skills.

Key Responsibilities

Strategic & Scientific Leadership

Develop and execute bioanalytical strategies to support preclinical and clinical development of ADCs and other biologics Lead development, optimization, and validation of bioanalytical methods (e.g., ELISA, ECLIA, LC-MS/MS, ligand-binding assays) for PK, ADA, and other biomarkers Represent Bioanalytical Sciences in regulatory meetings and cross-functional project teams

Laboratory & Facility Oversight

Oversee day-to-day operations of the Bioanalytical Lab, ensuring compliance with GLP, GCP, ICH, and internal quality standards Ensure equipment calibration, qualification, and maintenance are performed according to validated procedures Develop and implement SOPs, training curricula, safety protocols, and quality systems to maintain inspection readiness Lead preparation and execution of internal audits and inspections by health authorities

Team & Program Management

Build, lead, and mentor a team of scientists and technical staff; manage performance reviews and career development plans Oversee resource allocation, project timelines, and delivery of high-quality data for regulatory and clinical milestones Foster a culture of accountability, scientific rigor, and continuous improvement

Global and Cross-functional Collaboration

Coordinate with global bioanalytical and translational science teams to align platforms, analytical strategies, and data standards Collaborate with Clinical Development, Regulatory Affairs, Quality Assurance, and other stakeholders to support clinical and regulatory submissions Participate in global initiatives to improve harmonization of bioanalytical practices and data reporting

Regulatory & Quality Responsibilities

Author and review bioanalytical sections of regulatory submissions (e.g., INDs, BLAs, CTAs) Ensure compliance with international regulatory requirements including FDA, EMA, NMPA, and ICH guidelines (e.g., ICH E6, E14, M10) Lead or support regulatory inspections, addressing inquiries related to bioanalytical methods, data integrity, and laboratory operations

Qualifications

Education

Ph.D. in Pharmacology, Biochemistry, Analytical Chemistry, or a related field is preferred M.S. with extensive industry experience (12+ years) will also be considered

Experience

Minimum 10 years of industry experience in bioanalytical sciences, with direct involvement in clinical-stage biologics or ADC development At least 5 years of leadership experience in a laboratory setting, preferably at the Associate Director level or higher Proven expertise in method development, validation, and troubleshooting for PK/ADA assays Hands-on experience managing GLP/GCP-compliant labs and implementing CAPA systems Working knowledge of data integrity principles (21 CFR Part 11) and equipment/facility qualification

Skills

Strong leadership and team-building abilities; capable of fostering high-performance teams In-depth technical expertise in ligand-binding assays, LC-MS/MS, immunoassays, and hybrid methodologies Excellent communication skills with demonstrated success in cross-functional and cross-cultural collaborations Proficiency in regulatory documentation and audit preparedness Ability to work in a dynamic, fast-paced, and mission-driven environment with shifting priorities

Seniority level

Seniority level Director Employment type

Employment type Full-time Job function

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