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The job details are as follows:
Who We Are
We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.
United Therapeutics (Nasdaq: UTHR) seeks to travel down the corridors of indifference to develop treatments for rare, deadly diseases. We were founded in 1996 by a family seeking a cure for their daughter’s pulmonary arterial hypertension (PAH). Today, we have six FDA-approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF).
The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need. For this reason, we are working to create manufactured organs to address the shortage of kidneys, hearts, lungs, and livers available for transplant. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.
Who You Are
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 https://www.unither.com/careers/benefits-and-amenities
United Therapeutics Corporation is an Equal Opportunity Employer, including veterans and individuals with disabilities.
Skills Required
- Associate Degree in information technology, chemical engineering, bioengineering, or applicable scientific/engineering discipline
- 10+ years (Associate's), 8+ years (Bachelor's) or 6+ years (Master's) experience in an FDA regulated pharmaceutical manufacturing environment delivering/administering MES or electronic batch record systems
- Demonstrated experience delivering electronic batch records, electronic forms, or equivalent in a GxP environment
- Technical expertise authoring and maintaining electronic batch records and electronic forms in a commercial platform
- Excellent project management skills
- Superior database maintenance and 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
- Bachelor's or Master's Degree in information technology, chemical engineering, bioengineering or applicable scientific/engineering discipline
- Certified Project Management Professional (PMP) - PMI
- Technical expertise with authoring and maintaining electronic batch records and electronic forms in Opstrakker
United Therapeutics Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about United Therapeutics and has not been reviewed or approved by United Therapeutics.
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Healthcare Strength — Coverage breadth is positioned as comprehensive with the employer paying most medical, dental, and vision premiums, alongside telehealth, EAP, FSAs, and wellness initiatives. Fertility support is emphasized through full IVF coverage.
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Parental & Family Support — Paid parental leave for all parents with additional time for birthing parents, plus adoption and surrogacy assistance, lactation rooms, and milk‑shipping indicate robust family support. Subsidized onsite childcare is available at key campuses and broader family solutions are offered through a national provider.
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Strong & Reliable Incentives — Annual cash bonus opportunities are a consistent part of total rewards, complemented by equity eligibility and an employee stock purchase plan. Feedback suggests these incentives are widely available across many roles.
United Therapeutics Insights
What We Do
United Therapeutics Corporation is a biotechnology company focused on the development and commercialization of unique products to address the unmet medical needs of patients with chronic and life-threatening conditions. We currently have five approved products on the market, and a long-term mission of providing an unlimited supply of transplantable organs for those who need them! Our employees can be found collaborating across the United States, Europe and Asia. As a group, we are relentless in our pursuit of “medicines for life” and continue to research and develop treatments for cardiovascular and pulmonary diseases, pediatric cancers, and other orphan diseases. #WeAreUnitherians





