Responsibilities:
- Plan and oversee day-to-day operations of one or more laboratories/projects.
- Ensure laboratory resources (reagents/materials/equipment/facilities) meet objectives.
- Support a quality and compliant testing environment (GxP, training/documentation, methods, personnel).
- Manage project timelines with immunology leads; plan long-term resources and test scheduling.
- Maintain process/procedure alignment; share best practices.
- Oversee laboratory staff activities; provide technical guidance on safety and regulatory compliance.
- Monitor operations for compliance.
- Develop staff; ensure onboarding/training and adequate staffing levels.
- Support test method life cycle management (documentation, suitability/trending, maintenance).
- Support completion of analytical deliverables; assist with evaluation of new technologies/improvements.
- Review/evaluate data and recommend actions; collaborate with internal/external partners.
- Prepare key documents and ensure adherence to quality/safety/regulatory requirements.
- Track/manage budgets and advise on deviations.
Qualifications (Required):
- PhD +4 years OR MS +6 years OR BS +9 years in relevant industry experience.
- Ligand binding assay experience: ELISA, RIA, Luminex, MSD, Ortho VITROS, and automated platforms.
- Demonstrated team leadership/management; strong organization/prioritization and project management.
Skills/Additional Qualifications (Preferred):
- Strong written/verbal communication; ability to liaison with stakeholders.
- Understanding of GXP; supervisory knowledge.
- Creative problem-solving; deadline/deliverable focus; excellent technical/analytical judgment.
Benefits:
- Health and wellbeing benefits and at least 14 weeksβ gender-neutral parental leave.