AmpSeq programme Director- FTC

About the Position

AmpSeq Programme Director - FTC

We are seeking a dynamic and experienced AmpSeq Programme Director to lead our strategic growth platform within the life sciences sector. This role is pivotal in driving revenue, customer conversion, operational scale-up, service readiness, and programme outcomes across global stakeholders.

Responsibilities

• Business Impact: Lead the AmpSeq programme as a strategic growth platform, driving delivery of revenue, customer conversion, operational scale-up, service readiness, and programme outcomes across global stakeholders.
• Innovation & Change: Direct cross-functional change across NGS workflows, portal adoption, panel design, pilot execution, manufacturing scale-up, BioIT support, quality controls, and customer onboarding.
• Type of Work: Balance strategic programme leadership with operational issue resolution, ensuring near-term delivery risks are managed while building a sustainable future-state operating model.
• Key Stakeholders: Partner with global Operations, Commercial, Product Development, Innovation Hub, BioIT, Quality, Supply Chain, Finance, PMO, site leadership, and senior executives to align priorities and unblock delivery.
• Communications: Provide clear programme updates, escalation packs, decision logs, risk summaries, KPI reporting, and leadership communications for operational reviews, steering committees, and executive forums.
• People Management: Lead through direct and matrixed teams, setting expectations, assigning accountable owners, clarifying decision rights, and supporting capability development across programme workstreams.
• Process Oversight: Own the programme governance model, including operational huddles, Tier 2 escalation reviews, steering committee decisions, intake and questionnaire review, action tracking, decision tracking, and risk management.
• Subject Matter Expertise: Apply a strong understanding of NGS services, AmpSeq customer workflows, design-to-pilot processes, kit manufacture, service delivery, BioIT dependencies, quality expectations, and operational scale-up.
• Continuous Improvement: Identify and drive improvements in turnaround time, first-time-right performance, traceability, inventory management, workflow standardisation, dashboarding, and operational handoffs.
• Data & Metrics: Establish and manage KPIs for revenue progression, opportunity conversion, panel design performance, pilot status, turnaround time, manufacturing readiness, capacity, quality, and customer delivery.
• Physical Demands: Primarily office, meeting, and virtual work, with periodic site visits to laboratory, manufacturing, and service environments.
• Policy & Standards Compliance: Ensure programme activities comply with LGC policies, quality expectations, EHS requirements, customer commitments, data controls, and relevant operational standards.
• Other Duties As Assigned: Perform other duties as required to support AmpSeq growth, business continuity, and strategic delivery priorities.

Requirements

Essential Knowledge and Qualifications:

• Degree or equivalent experience in life sciences, molecular biology, genomics, biotechnology, operations, programme management, or a related discipline.
• Significant experience leading complex cross-functional programmes in life sciences, genomics, laboratory services, manufacturing, operations, or commercial delivery environments.
• Demonstrated ability to manage strategic programmes with multiple workstreams, dependencies, risks, stakeholders, and senior leadership governance requirements.
• Strong understanding of operational scale-up, customer onboarding, service delivery, supply chain dependencies, quality requirements, and process governance.
• Experience using dashboards, action logs, decision logs, risk registers, and KPI reporting to drive accountability and programme delivery.
• Strong communication skills, including the ability to simplify complex operational and technical issues for executive, commercial, technical, and site-based audiences.

Desired Knowledge and Qualifications:

• Experience with NGS, AmpSeq, KASP, FlexSeq, or comparable high-throughput genotyping service platforms.
• Experience working across multiple global sites and managing delivery through matrixed teams.
• Formal project or programme management qualification, such as PMP, PRINCE2, Lean, Six Sigma, or equivalent practical experience.
• Experience with ERP, LIMS, Salesforce, Tableau, Smartsheet, Microsoft Project, or other operational planning and reporting tools.
• Familiarity with customer-facing technical programmes, product launch readiness, validation, manufacturing readiness, and service implementation.

We Offer

• Comprehensive medical, dental, and vision benefits for employees and dependents.

About the Company

LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Our high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range.

Our tools play a key role in customer workflows from discovery applications through to commercial manufacture and enable its customers to: bring new diagnostics and therapies to market; progress research and development; optimize food production; and continuously monitor and enhance the quality of food, the environment, and consumer products.

LGC’s 175+ years of scientific heritage, combined with a track record of innovation and value-enhancing acquisitions, has enabled the company to build its product portfolio and expertise, and develop deep relationships with customers, industry partners, and the global scientific community. Join us and help us achieve our mission of Science for a Safer World!

Our kit and component manufacturing sites are situated across the US (Middleton, Petaluma, and Novato) and Europe (Berlin and Lystrup) and are underpinned by either ISO 13485 or ISO 9001 compliance. These capabilities support a wide portfolio of off-the-shelf components and kits critical to NGS workflows including magnetic beads, oligos, enzymes, and library prep kits. Additionally, our primary manufacturing capabilities enable customization and bulk (OEM) manufacture of reagents such as key NGS enzymes for high volume applications.

This position requires current U.S. work authorization. We are unable to sponsor or assume sponsorship for temporary visas (including H‑1B, H‑2B, OPT, O‑1, TN)

Job Location

• Work Arrangement: Remote
• Country: United States