The job details are as follows: What We Do We build on the strength of our research and development expertise and a distinctive, entrepreneurial culture that encourages diversity, innovation, creativity, sustainability, and, simply, fun. Since inception, our mission has been to find a cure for pulmonary arterial hypertension and other life-threatening diseases. Toward this goal we have successfully gained FDA approval for five medicines, we are always conducting new clinical trials, and we are working to create an unlimited supply of manufactured organs for transplantation. We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation (PBC). Our public benefit purpose is to provide a brighter future for patients through (a) the development of novel pharmaceutical therapies; and (b) technologies that expand the availability of transplantable organs. At the same time, we seek to provide our shareholders with superior financial performance and our communities with earth-sensitive energy utilization. Our company was founded by an entrepreneur whose daughter was diagnosed with a life-threatening condition. She sought to find treatment options and a cure for her daughter and patients like her. We are founder-led, and relentless in our pursuit of “medicines for life”. We continue to research and develop treatments for cardiovascular and pulmonary diseases, and other orphan diseases. With over 100,000 patients on the organ transplant waitlist and only a fraction receiving the lifesaving organ they require, there is a great need for additional sources of transplantable organs. At Miromatrix, a leader in regenerative medicine and a subsidiary of United Therapeutics Corporation, we are working to address this unmet need by bioengineering human organs to help save and improve patients’ lives. Join our team as we continue to make history by developing life-saving therapies to help patients with liver and kidney disease. How you’ll contribute: The Senior Process Engineer will be responsible for the development and maintenance of new and existing automation control systems that will enable new R&D production processes and manufacturing of novel bioengineered organs. Additionally, this position will support maintenance, troubleshooting, and repairs of various facility equipment and other critical utilities. Responsibilities will include serving as the project point person from conceptual plan, detailed design, and construction. Identify and implement process improvement opportunities for manufacturing Program PLC hardware (Rockwell – Allen Bradley) Develop prototype electrical cabinets – with documentation for manufacturing implementation Troubleshoot problems with PLC software, processes, and hardware Maintain and repair existing electrical and mechanical systems PLC control systems, critical facilities equipment, and utilities Source and install appropriate replacement components Inspect systems to ensure they meet applicable safety/quality requirements Communicate and collaborate cross-functionally in the design and development of systems Independently manage small to large-scale projects effectively from planning, design/concept, and execution Apply systematic thinking processes and technical knowledge to independently address a broad range of non-routine to complex problems Establish good preventative maintenance practices For this role you will need: Minimum Requirements Bachelor’s Degree in electrical engineering 5 years of related industry experience Proficiency in Rockwell/Allen Bradley hardware and software (min. 2 years of experience) Electrical documentation and drafting, with a preference on AutoCAD Strong mechanical system troubleshooting and general aptitude Knowledgeable of process control systems Experience in problem solving, negotiations, presentation and collaborative team-building across multiple geographies and cultures, as well as external parties Ability to determine customer needs to develop project specifications and scope Interpret and implement specifications Preferred Qualifications Experience with 21 CFR Part 11 compliant data management Experience with designing and qualifying GMP production systems and facilities At United Therapeutics you’ll realize quickly that it is not an ordinary place to work! When you join our company, you will learn, grow, contribute, have fun, and be challenged... all while making a difference in the lives of our patients. While United Therapeutics does not require vaccination for Covid-19 at this time, we strongly encourage all employees and visitors to remain up to date on vaccinations and boosters to protect one another from illness. Employees working in customer-facing roles must adhere and comply with customers’ credentialing guidelines, which may require vaccination against Covid -19, the influenza virus, and other illnesses that could be harmful to healthcare staff and patients. United Therapeutics Corporation is an Equal Opportunity/Affirmative Action Employer - EOE Minorities / Females / Protected Veterans / Individuals with Disabilities We strive to be an organization that engages the minds, hearts, and most spirited efforts of each of our employees. Our sense of purpose transforms what we do from work into mission, occupation into vocation and achievement into success. We challenge our employees with innovative and revolutionary projects, offer an environment which fosters high-level job performance and provide a highly competitive total rewards package. This is what makes United Therapeutics a stimulating place to work.