Director, Bioanalysis (TLM / Large Molecules)

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QPS Story:

QPS is a full-service contract research organization (CRO) supporting pharmaceutical, biotechnology, and medical device companies across the drug development lifecycle. Our services span neuropharmacology, DMPK, toxicology, bioanalysis, translational medicine, and clinical research (early phase through Phase IV). We are driven by science, collaboration, and a shared commitment to improving human health and quality of life. Our teams thrive in a culture that values innovation, accountability, teamwork, and continuous development, where strong performance is recognized and rewarded. Job Overview We are seeking a Director, Bioanalysis to lead assigned units within the Translational Medicine (TLM) department at QPS. This role blends scientific leadership with operational oversight, regulatory responsibility, and client partnership. As a senior member of the TLM Management Team, you will act as a subject matter expert, provide final input on QA/regulatory matters, and serve as a key point of contact for client and sponsor needs. You will also help drive scientific and operational improvements, support new initiatives, and contribute to expanding capabilities and business opportunities. What you will do Lead and oversee assigned bioanalytical units within TLM Serve as scientific SME and final decision-maker for regulatory and QA matters Act as primary liaison for client and sponsor inquiries, study support, and issue resolution Select appropriate assay methods and platforms aligned with client needs and study requirements Review and develop scientifically sound, compliant proposals Support onboarding and implementation of new technologies and platforms Monitor, troubleshoot, and resolve environmental and equipment-related issues Foster a collaborative, high-performing team focused on quality and timelines Share insights and contribute to continuous improvement across TLM operations Work Location This job will be 100% QPS-office/facility based What you bring Experience in a regulated laboratory environment is required Strong preference for experience within a CRO environment providing translational medicine and/or bioanalytical services One of the following education/experience combinations: Ph.D. + 12+ years relevant industry experience (or 10+ years CRO experience) Master s + 17+ years relevant industry experience (or 13+ years CRO experience) Bachelor s + 18+ years relevant industry experience (or 16+ years CRO experience) A strong leader with excellent communications skills and the ability to connect with clients and sponsors Why QPS Collaborative, science-driven environment with strong team support Clear career development pathways aligned with individual goals Performance-based bonuses and merit increases Comprehensive benefits package, including 401(k) match, life/AD&D, and disability coverage Park-like campus setting in Newark, Delaware Employee-focused committees that shape workplace experience

QPS, LLC

is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.