Associate Director, Reagent Development

Guardant Health•Palo Alto, CA

7d•$182,200 - $250,500•Hybrid

About The Position

The Associate Director Reagent Development leads a team of development scientists in the design, development, and optimization of next-generation sequencing (NGS) reagents for use within Guardant Health clinical laboratory products. The role guides reagent programs from early-stage proof of concept through successful internal implementation, and is accountable for ensuring that all development, formulation, and internal scale-up activities adhere to GMP and ISO 13485 quality standards in support of clinical testing operations. This position is a replacement requisition for an existing role.

Requirements

Ph.D. in Biochemistry, Molecular Biology, Chemistry, or a closely related discipline; an equivalent combination of education and experience may be considered.
7-12 years of industry experience in life sciences, biotechnology, or clinical diagnostics, including 3+ years in a management or leadership role.
Deep biochemistry knowledge, with a proven track record developing and optimizing complex biochemical systems, enzymology, and nucleic acid interactions.
Extensive hands-on experience developing reagents, kits, or assays specifically for next-generation sequencing.
Demonstrated success in taking at least one NGS reagent or relevant formulation from concept through design transfer and manufacturing implementation.
Direct experience developing products under strict design control processes within an ISO 13485 and/or cGMP compliant environment.
Familiarity with CLIA/CAP guidelines and the 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.
Excellent written and oral communication and presentation skills, including the ability to present to cross-functional partners and senior leadership.
Strong strategic thinking paired with a willingness to engage hands-on with the science.
Excellent attention to detail and documentation rigor.
Ability to multi-task, prioritize competing demands, and remain flexible with tasks and schedules.

Nice To Haves

Experience managing raw material supply chains and interacting with external vendors for critical reagent components.
Demonstrate curiosity, sound judgment, and the ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve the efficiency, effectiveness, and quality of work.

Responsibilities

Direct a team of development scientists, fostering a culture of flexibility, adaptability, scientific rigor, innovation, and teamwork.
Gain strategic alignment with leaders and deliver on project goals, allocate resources, and manage timelines in collaboration with clinical project management to ensure assay and reagent development milestones align with product and clinical laboratory needs.
Capability and desire to complement their team’s work product with individual contributions in the lab and with drafting program and protocol documentation and interest to provide mentorship outside of their direct line of reporting.
Demonstrated capabilities to successfully manage development activities under design control and change management processes.
Leverages deep technical expertise and executive-level influence to guide resolution of complex biochemical and molecular challenges, provide strategic direction on reagent optimization, and effectively persuade stakeholders to successful resolution of critical issues in clinical testing.
Lead the end-to-end development, formulation, and optimization of enzymes, buffers, and chemical reagents for internal NGS applications, including library preparation, target enrichment, and sequencing chemistries.
Versant in automated liquid handling systems, including method development criteria and limitations
Design and execute robust verification and validation (V&V) studies tailored to internal manufacturing workflows.
Lead technical design reviews and phase-gate meetings for internal deployment.
Partner closely with Product Development, Operations, Quality Assurance, and Supply Chain to ensure seamless design transfer, scale-up, and internal production of NGS reagents.
Comfortable with ERP and eQMS systems
Establish critical quality attributes (CQAs) and stability testing protocols for raw materials and finished reagents.
Oversee and contribute to the generation of design control and validation documentation, including standard operating procedures (SOPs), batch records, and quality control specifications required for CLIA/CAP and FDA compliance.
Collaborate with the Bioinformatics team to ensure reagent specifications meet required assay performance metrics and turnaround times.
Participate in audits with external vendors supplying critical reagent components.
Ensure all reagent development and internal manufacturing activities comply with ISO 13485 standards, Good Manufacturing Practices (GMP), and the internal Quality Management System (QMS).
Responsible for ensuring customer requirements are determined, documented and met.
Responsible for identifying and providing adequate resources and training to ensure effective work performance which includes meeting regulatory, statutory and customer requirements while also supporting and maintaining the effectiveness of the quality system.
Perform other duties as assigned

Benefits

Guardant has defined days for in-person/onsite collaboration and work-from-home days for individual-focused time.
The annualized base salary ranges for the primary location and any additional locations are listed below. This range does not include benefits or, if applicable, bonus, commission, or equity.
Each candidate’s compensation offer will be based on multiple factors including, but not limited to, geography, experience, education, job-related skills, job duties, and business need.
Guardant Health is committed to providing reasonable accommodations in our hiring processes for candidates with disabilities, long-term conditions, mental health conditions, or sincerely held religious beliefs.
A background screening including criminal history is required for this role.
GH will consider qualified applicants with criminal arrest or conviction histories in a manner consistent with applicable law including but not limited to the LA County Fair Chance Policies and the Fair Chance Act (Gov. Code Section 12952).
Guardant Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
All your information will be kept confidential according to EEO guidelines.
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Please visit our career page at: http://www.guardanthealth.com/jobs/