Associate Process Engineer, Print Operations

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. How you’ll contribute The Associate Process Engineer is responsible for participating and supporting lab scale production, process development, and process validation. The Associate Process Engineer will also provide inputs to process engineering design as well as contribute to ongoing process analysis and improvements. This role will also be responsible for analyzing and documenting the results of experiments to prepare for tech transfer to manufacturing (GMP). Deliver quality biomaterial and 3D printed products to internal collaborators by identified timeline(s) with some oversight or consultation with management, including raw materials QC, bioink mixing, 3D printing, and post processing of 3D printed parts Document standard processes for production and post processing, ensure compliance to specifications, and report abnormalities in product or processes to the subject matter experts Support the development, implementation, and validation of methods used to assess biomaterials and 3D printed parts, their analysis, and any post processing requirements Support the scale up and continuous improvement of end-end processes that are transferred to print operations while maintaining consistent product quality Collaborate with teams to receive and provide feedback supporting process analysis and process improvements Perform all other duties as assigned For this role you will need Minimum Requirements Bachelor’s Degree in materials science, chemistry, chemical, mechanical or biomedical engineering, or a related field 1 years of experience in materials science, chemistry, chemical, mechanical or biomedical engineering (or equivalent) with a Bachelor's Degree 1 years of experience in wet laboratory operations 1 years of experience with SLA/DLP based 3D printing biomaterials and print process methods Proficiency with data compilation, presentation, and reporting as well as a general understanding of good data practices/data governance principles Experience with biomaterial formulations and 3D printing processes and operations Proficient in statistical analysis (JMP, Excel, and/or Graph Pad Prism) Experience utilizing an electronic laboratory notebook (ELN) similar to benchling Experience in scaling up laboratory processes/operations Ability to work independently and as part of a team Preferred Qualifications Master’s Degree in materials science, chemistry, chemical, mechanical or biomedical engineering, or a related field 1 years of experience in a manufacturing environment 1 years of experience with design of experiments (DOEs), process development, and process validation 1 years of experience with product development and tech transfer to manufacturing 1 years of experience in change management Knowledge of quality control principles and methodology Knowledge of GxP (GDP, GLP, and GMP) Experience with biocompatibility and sterilization Knowledge of perfusion bioreactors and general cell culture principles 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.