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Lead Master Data Analyst

Finance & Administration | Research Triangle Park, NC | Full Time

Job Description

About Us:

Humacyte's mission is to become the leading company in novel, off-the-shelf extracellular matrix tissue products, and especially those that could provide lifesaving improvements in treatments for vascular conditions.

Humacyte, Inc., a biotechnology pioneer, discovers, develops and delivers innovative, award winning human biotherapies.  We are currently developing multiple vascular tissue engineered therapies and expanding our business model.  With a broad pipeline of potential new therapy applications, we continue to build our organization and scientific teams.


The Lead Master Data Analyst will be steward of Master Data for Humacyte.  They will accountable for data integrity and leverage internal as well as external collaboration to insure any additions or modifications incorporate an end to end view.  The Lead Master Data Analyst will leverage and optimize the capabilities of Master Data Management in Great Plains (Enterprise Resource Planning System, Microsoft Dynamics) and Without Wire Inventory System (Warehouse Management System) while adhering to the Humacyte Change Control process. These detailed responsibilities include but are not limited to:

  • Own the entry and integrity of supply chain master data
  • Manage the process for material creations, modifications, and extensions while working in close collaboration with technology transfer team to ensure identified items are available for use on the site
  • Develop and implement plans that achieve the strategic and tactical requirements of Master Data Management at Humacyte
  • Develop and maintain a collaboration cadence with key stakeholders (i.e. Manufacturing, Finance, Quality, Supply Chain, & Purchasing) to align strategies with local supply/demand
  • Facilitate master data initiatives and projects
  • Develop processes to monitor and flag missing or inconsistent Master Data
  • Regularly review and enforce data quality standards internally and externally
  • Coordinate and track package introductions and changes to ensure product availability for New Product/Pack Introductions (NPIs), Regulatory copy changes, Pack Optimization Strategies, product transfers, and site performance improvement initiatives
  • Create, maintain, and manage detailed project plans in collaboration with all required functional areas for new items and pack changes (Pack design, patient focus group studies, component specs/drawings, testing results, key line trials, regulatory filings) to ensure critical supply milestones and regulatory requirements are met
  • Manage all applicable SOP(s) for master data management
  • Work with QA and local stakeholders to define and continuously improve the change control strategy for the management of materials.


  • BA/BS in Business, Computer Science, Supply Chain, Engineering, or related field of study or applicable job experience
  • Direct experience in regulated environments (cGMP, FMCSA, OSHA, EPA) is required
  • Detailed knowledge of Master Data Management.   Experience with Great Plains (Microsoft Dynamics) and/or Withoutwire Inventory Science software is preferred

Bonus Points:

  • Demonstrate a background in Master Data Management (MDM)
  • Experience in MDM process design and change management
  • Insure master data integrity and quality across processes and functions
  • Applicable functional experience in item lifecycle maintenance in a regulated environment (cGMP, FMCSA, OSHA, EPA) 
  • Maintain attention to detail, while completing multiple or repetitive tasks


  • Stock Options
  • 401k Plan with Matching
  • Medical, Vision and Dental Plans
  • Long Term/Short Term Disability
  • Life Insurance
  • 3 Weeks’ Vacation
  • 5 Personal Floating Days
  • 8 Sick Days
  • 6 Company Holidays
  • Career Development and Training