Senior Vice President, Operations

Slingshot Biosciences•Emeryville, CA

About The Position

Slingshot Biosciences is a fast-growing life sciences company with a platform technology and paradigm-shifting mission to make precision-engineered cell mimics the gold standard for all cell-based assay controls. We are transforming cell-based applications with the most robust, scalable, and reproducible controls available, including TruCytes™ Biomarker controls, SpectraComp® compensation controls, ViaComp® cell health controls, and FlowCytes® instrument controls. Our TruCytes cell mimics precisely replicate real cells’ optical and biochemical properties - without the sourcing, quality, or cost challenges of traditional controls. Trusted in cell-based applications across cell therapy, drug development, and diagnostics, they empower process and analytical development, quality control, potency assessments, multi-site validations, clinical research studies, and assay development and validation. Slingshot is seeking motivated, creative team members who think outside the box. We empower employees to own their work, contribute ideas quickly, and improve processes. Come join our cross-disciplinary and world-class team that is delivering game-changing solutions for cell-based applications! We are seeking a visionary and execution-focused Senior Vice President of Operations to lead and scale our end-to-end operations as we transition from research-use-only (RUO) products into regulated markets. This executive role sits at the intersection of production, regulatory affairs, quality systems, and supply chain, and is responsible for driving product development from concept through scale-up and commercialization. The ideal candidate is both a strategic leader and hands-on builder with deep expertise in biotechnology manufacturing, regulatory strategy, and global supply chain operations — ensuring delivery of high-quality products that enable advancements in cell-based research, diagnostics, and therapeutics worldwide.

Requirements

Advanced degree (PhD, MS, or equivalent) in Life Sciences, Engineering, or related field
15+ years of progressive leadership experience in biotechnology or medical device industries
Proven track record in scaling operations, including manufacturing and supply chain functions
Proven track record in regulatory strategies in product development and commercialization
Deep expertise in biotechnology manufacturing, regulatory affairs, quality systems, and supply chain operations
Experience with cell-based products, cell mimic materials, or related technologies
Strong knowledge of ISO standards, USP, and cGMP requirements
Experience supporting customer regulatory submissions and technical documentation
Expertise in process development, tech transfer, supplier qualification, and supply chain scaling
Expertise in Netsuite or similar ERP system
Proven ability to lead complex, cross-functional organizations in fast-paced environments
Strong strategic planning, budgeting, and P&L management experience
Demonstrated ability to set and achieve operational and company-wide goals
Entrepreneurial mindset with a hands-on, builder-oriented approach
Legal authorization to work is required for all roles.

Nice To Haves

Expert user of Netsuite or a similar ERP system

Responsibilities

Lead and scale end-to-end operations, including manufacturing, supply chain, and logistics
Lead facility design, equipment qualification, process validation, and technology transfer
Drive operational excellence via automation, lean manufacturing & continuous improvement
Plan, budget, and manage operational capacity across custom and catalog product lines
Partner with R&D, Commercial, and Finance to align product development
Develop and execute regulatory strategies to support product commercialization
Support customer regulatory submissions by providing technical documentation and guidance
Maintain strong relationships with regulatory agencies and industry partners
Stay current with evolving regulatory requirements and industry best practices
Design and implement robust quality systems compliant with: USP standards, ISO 13074, ISO 13485, ISO 9001, cGMP and applicable regulatory requirements
Oversee QA/QC functions and continuous improvement initiatives
Ensure effective CAPA systems and audit readiness
Develop and execute a robust, scalable end-to-end supply chain strategy aligned with company growth and regulatory requirements
Establish and optimize demand planning, inventory management, and S&OP (Sales & Operations Planning) processes
Lead supplier qualification, auditing, and performance management in compliance with ISO and cGMP standards including dual sourcing for critical materials
Oversee logistics, distribution, and cold chain (if applicable), ensuring on-time delivery to customers and partners
Build and manage relationships with key suppliers, CDMOs, and logistics providers