Director, Reagent Development

Veracyte•South San Francisco, CA

8d•$216,000 - $240,000•Onsite

About The Position

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way – it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. We are seeking a highly driven and experienced Director of NGS Reagent Development to lead a dedicated team of development scientists in design, development, and optimization of NGS reagents specifically for use within our clinical laboratory products. Leveraging your deep expertise in biochemistry and molecular biology, you will guide the team from early-stage proof-of-concept through successful internal implementation. You will ensure all development, formulation, and internal scale-up activities maintain strict adherence to GMP and ISO 13485 quality standards to support our rigorous clinical testing operations.

Requirements

Ph.D. in Biochemistry, Molecular Biology, Chemistry, or a closely related discipline.
10+ years of industry experience in life sciences, biotechnology, or clinical diagnostics, with at least 5+ years in a management or leadership role.
Deep Biochemistry Knowledge: Proven track record of developing and optimizing complex biochemical systems, enzymology, and nucleic acid interactions.
NGS Mastery: Extensive hands-on experience developing reagents, kits, or assays specifically for Next-Generation Sequencing
Reagent Development Lifecycle: Demonstrated success development of least one NGS reagent or relevant formulation from concept through design transfer and manufacturing implementation.
GMP/ISO Regulated Environments: Direct experience developing products under strict design control processes within an ISO 13485 and/or cGMP compliant environment.
Clinical Lab Standards: Familiarity with CLIA/CAP guidelines and the specific quality and regulatory requirements for scaling reagents within a high-throughput clinical laboratory.
Expertise in Design of Experiments (DoE), statistical analysis, and establishing rigorous QC metrics for reagent formulation.

Nice To Haves

Excellent cross-functional communication and presentation skills.
Strong strategic thinking paired with a willingness to "roll up your sleeves" and engage with the science.
Experience managing raw material supply chains and interacting with external vendors for critical reagent components.

Responsibilities

Direct, mentor, and grow a team of research and development scientists, fostering a culture of scientific rigor, innovation, and continuous improvement.
Define project goals, allocate resources, and manage timelines to ensure assay and reagent development milestones align with product and clinical laboratory needs.
Provide technical guidance and troubleshooting support for complex biochemical and molecular challenges encountered during reagent optimization.
Lead the end-to-end development, formulation, and optimization of enzymes, buffers, and chemical reagents for internal NGS applications (e.g., library preparation, target enrichment, sequencing chemistries).
Design and execute robust verification and validation (V&V) studies tailored for the manufacturing workflows.
Establish critical quality attributes (CQAs) and stability testing protocols for raw materials and finished reagents.
Ensure all reagent development and internal manufacturing activities strictly comply with ISO 13485 standards, Good Manufacturing Practices (GMP), and our internal Quality Management System (QMS).
Oversee the generation of meticulous design control and validation documentation, including standard operating procedures (SOPs), batch records, and quality control specifications required for CLIA/CAP compliance.
Lead technical design reviews and phase-gate meetings for internal deployment.
Partner closely with Product Development, Operations, Quality Assurance, and Supply Chain teams to ensure seamless design transfer, scale-up, and internal production of NGS reagents.
Collaborate with Bioinformatics team to ensure reagent specifications meet required assay performance metrics and turnaround times.