Director, Bioanalysis (TLM Large Molecules)

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

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)
• Masters 17 years relevant industry experience (or 13 years CRO experience)
• Bachelors 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 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 addition QPS LLC is a federal contractor and desires priority referrals of protected veterans.