Director of Laboratory Operations - Vital Tears

Saving-SightKcmo, MO
1dOnsite

About The Position

This mission centered position is responsible for overseeing end-to-end production of Autologous Serum Eye Drops (ASED) at commercial scale and leading an aseptic operations team across collection intake, aseptic filling, labeling/packaging, QA/QC interface, and distribution, ensuring compliant, safe, reliable, and cost effective operations.

Requirements

  • Knowledge of good manufacturing practices and ability to work within a regulated framework.
  • Knowledge of aseptic processing best practices, environmental controls, and cleanroom discipline.
  • Working knowledge of Lean/Six Sigma methodologies.
  • Strong organizational skills, critical thinking and problem-solving abilities, and attention to detail.
  • Ability to build and execute a capacity model aligned to meet demand.
  • Ability to scale to 50k+ annual orders.
  • Working knowledge of Microsoft operating systems, Microsoft Office, general database, and web-based applications.
  • Minimum of five years' experience leading teams to meet production goals.
  • GMP, aseptic processing, deviation/CAPA, validation, and audit experience.
  • Minimum of three years' experience in sterile/aseptic GMP or healthcare manufacturing.
  • Must maintain a valid driver's license, current auto insurance, and an acceptable driving record determined by the organization.
  • Must have reliable transportation.
  • Hepatitis B vaccination or signed declination is required.
  • In the last 5 years, the candidate must have 0 major moving violations and less than 3 minor moving violations.

Nice To Haves

  • Bachelor's degree or an equivalent combination of education and experience from which comparable knowledge, skills, and abilities have been acquired.
  • Experience with patient specific or lot specific operations.
  • Experience in Biologics manufacturing is a plus.

Responsibilities

  • Lead day to day manufacturing operations for ASED: staffing, scheduling, floor management, and performance for ~25 FTEs across multiple shifts.
  • Generate and analyze key performance indicators and other metrics to monitor all aspects of laboratory performance for operational performance.
  • Achieve OTIF (On-Time In-Full) ≥ 98%, RFT (Right First Time) ≥ 99%, scrap/rework ≤ target, and COGS (Cost of Goods)/order reduction within the first 12-18 months of employment.
  • Support the annual budgeting by leveraging data-driven analysis to optimize resource allocation, reduce costs, and ensure ongoing evaluation of equipment and materials for operational efficiency.
  • Maintain accurate records and documentation to support effective, quality-focused laboratory operations, including ensuring aseptic processing best practices, environmental controls and cleanroom discipline.
  • Achieve service levels for JIT (Just In Time), yield, throughput, cost per order, and right first time metrics to scale from 25k to ~50k orders/year over the next 5 years .
  • Serve as a key contributor to the Vital Tears operations team.
  • Partner cross-functionally with Supply Chain, Customer Operations, Regulatory, IT, and Finance to align strategy and drive execution of key operational initiatives.
  • Partner with QA to maintain change control, CAPA (Corrective Action Preventive Action), deviation/NC (Non-conformance) management, batch record review/release, and audit readiness.
  • Support organizational goals through collaboration and problem-solving with a process improvement mindset.
  • Recruit, develop, and retain talent; provide coaching and clear career paths.
  • Create and sustain a workplace culture aligned with Saving Sight and Vital Tears' mission, vision, and values while promoting safety, quality, data-driven decision-making, and continuous improvement.
  • Support development and optimization of the ERP and support systems in collaboration with IT, Patient Services and vendors.
  • Review and execute quality protocols such as procedure verifications, environmental monitoring, non-conformance reporting, and other quality and compliance activities applicable to laboratory operations.
  • Interface with external stakeholders and serve as the subject matter expert for laboratory operations.
  • Communicate effectively with team members, leadership, and external partners.
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