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The job details are as follows:

The Lead eBR Systems Analyst of Operational Technology will drive the use of GxP electronic forms and batch records to eliminate paper recording of production data. This role will serve as a liaison between OT functional areas deploying and using electronic forms and batch records, providing the highest level of customer satisfaction and partnership, ensuring that OT services are delivered as committed. This person will work closely with the GxP functional areas, vendors, and system owners to understand their current requirements and future roadmap. Additionally they will provide key technical support for various manufacturing and manufacturing support systems such as OpsTrakker, and other GxP Applications and in a regulated, validated environment.

• Independently lead project management activities, including defining the scope of the project; creating a project schedule; tracking project progress; communicating with stakeholders; identifying and resolving system issues; leading prioritization; and managing project risks
• Manage continuous improvement project portfolio: Evaluate managed GxP and Quality systems, identify opportunities, and make recommendations to Quality and GxP operations' leadership.
• Perform and/or coordinate GxP and Quality systems configuration changes for applications in collaboration with functional business units and external consultants
• Review system design and scope and execute plans to ensure application meet business requirements and identify gaps
• Plan and manage training to end users for modifications to existing processes and/or new functionalities
• Lead project and support initiatives, day-to-day support, and off-hour activities on a day-to-day basis
• Coach and guide peers/junior team members on Opstrakker and other systems' configuration and business processes
• Create documentation and procedures to support the implementation and maintenance of managed GxP and Quality systems
• Drive the use of GxP electronic forms and batch records to eliminate paper recording of production data
• Collaborate with cross-functional teams, and Technical Teams to identify and resolve issues
• Manage GxP and Quality systems' updates
• All other duties as assigned

Minimum Requirements

• Associate Degree in information technology, chemical engineering or bioengineering or an applicable scientific and/or engineering discipline preferred
• 10+ years of experience in an FDA regulated pharmaceutical manufacturing environment, with emphasis on delivering and administering MES, electronic batch record, or other systems with similar functionality with an Associate's Degree or
• 8+ years of experience in an FDA regulated pharmaceutical manufacturing environment, with emphasis on delivering and administering MES, electronic batch record, or other systems with similar functionality with a Bachelor's Degree or
• 6+ years of experience in an FDA regulated pharmaceutical manufacturing environment, with emphasis on delivering and administering MES, electronic batch record, or other systems with similar functionality with a Master's Degree
• Demonstrated experience delivering electronic batch records, electronic forms, or equivalent in a GxP environment
• Technical expertise with authoring and maintaining functionality of electronic batch records and electronic forms in a commercial platform
• Excellent project management skills
• Superior database maintenance / development experience
• Computer hardware / software validation and change control experience
• Knowledge and experience working in FDA CFR Part 11 compliant environment
• Experience working on small, fast paced project teams
• Ability to work under pressure and adhere to deadlines
• Good verbal and written communications skills
• Sound understanding of standard business practices

Preferred Qualifications

• Bachelor’s Degree in information technology, chemical engineering or bioengineering or an applicable scientific and/or engineering discipline preferred or
• Master’s Degree in information technology, chemical engineering or bioengineering or an applicable scientific and/or engineering discipline preferred
• Certified Project Management Professional (PMP)-PMI
• Technical expertise with authoring and maintaining electronic batch records and electronic forms in Opstrakker

At United Therapeutics, our mission and vision are one. We use our enthusiasm, creativity, and persistence to innovate for the unmet medical needs of our patients and to benefit our other stakeholders. We are bold and unconventional. We have fun, we do good.

Eligible employees may participate in the Company’s comprehensive benefits suite of programs, including medical / dental / vision / prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off & paid parental leave benefits, disability benefits, and more. For additional information on Company benefits, please visit