Senior Bioprocess Engineer - Cell Production & Process Development
United Therapeutics Corporation · Manchester, NH · 3 wk ago
On-siteEngineeringFull-time
We need to output HTML fragment with sections: h3 headings for sections present: About the role? Actually we have "Who We Are", "Who You Are", responsibilities (list of duties), Minimum Requirements, Preferred Qualifications, Job Location, Benefits maybe. Also Pay/Schedule not present. We should not repeat job title. Use h3 for section headings. Use ul/li for lists. Use p for prose. Remove boilerplate: "California, US residents click here." etc. Also remove EEO line. Also remove navigation etc. Keep substantive info.
We need to preserve all substantive info: description of company, mission, role responsibilities, requirements, preferred qualifications, location, benefits, flexible hours note.
We need to avoid filler like "commensurate with experience". Not present.
We need to output only HTML fragment, no html/body tags, no markdown fences.
Let's craft sections:
- About the Company (maybe heading "About the Company") but rule says use h3 for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). They gave examples but we can use other headings? Probably we should stick to those headings if content matches. We have "Who We Are" -> could be About the Company or About the role? Might be "About the Company". Not in list but we can still use h3? The instruction: "use for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule)." It says e.g., meaning those are examples, not exclusive. So we can use other headings as h3.
Thus we can have:
for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule)." It says e.g., meaning those are examples, not exclusive. So we can use other headings as h3.
Thus we can have:
About United Therapeutics
...
Who You Are
...
Responsibilities
- ... ...
Minimum Requirements
- ... ...
Preferred Qualifications
- ... ...
Job Location
...
Benefits
...
Also note flexible hours: mention in Job Location or maybe separate? Could add a note in Job Location paragraph. We must not include Pay/Schedule sections because not specified. We must remove duplicated lines: The responsibilities list appears duplicated in the posting; we need to include each duty once. Let's extract responsibilities bullet points from the text: - Plan and contribute to the execution of cell production runs to provide a reliable supply of primary and iPSC-derived cells for research and process development activities - Independently lead small-to-medium process development studies to develop, optimize, and scale robust, cGMP-compliant manufacturing processes for iPSC-derived cells, including study planning, execution, data analysis, risk identification, and communication of results and recommendations - Develop, author, review, and maintain laboratory procedures, records, technical reports, protocols, and other controlled documentation to support process development, technology transfer, and GMP readiness - Investigate process deviations, troubleshoot technical challenges, and identify opportunities for process improvements that enhance manufacturing robustness, consistency, efficiency, and scalability - Evaluate emerging technologies, equipment, and manufacturing strategies to support continuous improvement initiatives, including participation in the selection, acquisition, implementation, and lifecycle management of laboratory and manufacturing equipment - Foster and leverage synergistic interactions with other sub-groups in Organ Manufacturing (e.g., Analytical Development, Operations, Tissue Engineering, Quality, Manufacturing), as appropriate - Author technical reports, support regulatory and technical documentation, contribute to scientific publications, and present data to internal and external audiences - Perform other duties as assigned Now Minimum Requirements: It's a bit complex with alternatives. We need to preserve all info. Could list as bullet points: - Bachelor’s Degree in biomedical science, cell biology or related field OR Master’s Degree in biomedical science, cell biology or related field OR Doctor of Philosophy (PhD) in biomedical science, cell biology or related field - 5+ years of relevant experience in stem cell therapy, bioreactor cell production, scale up, regenerative medicine, tissue engineering with a BA/BS Degree OR 3+ years of relevant experience ... with a Master's Degree OR 1+ years of relevant experience ... with a PhD - Strong background in cellular process development and/or mid-scale cell production (2-10L) - Technical expertise in cell bioreactor culture, preferably Sartorius Ambr/B-DCU systems and/or vertical wheel bioreactors with scales up to 10L+ - Proficient with appropriate word processing, spreadsheet, presentation, and related standard software - Experience with laboratory instrumentation and data software - Excellent written and oral communication skills - Strong organizational skills and attention to detail - Ability to accommodate a non-traditional work schedule (e.g. Sun-Thu, Tue-Sat) and/or contribute to Weekend/Holiday work as needed - Previous industry experience Preferred But note "Previous industry experience Preferred" is actually under Minimum Requirements? It says "Previous industry experience Preferred Qualifications". Actually after Minimum Requirements block there is "Previous industry experience Preferred Qualifications". Might be part of Preferred Qualifications. Let's parse: The text: "Minimum Requirements Bachelor’s Degree in biomedical science, cell biology or related field or Master’s Degree in biomedical science, cell biology or related field or Doctor of Philosophy (PhD) in biomedical science, cell biology or related field5+ years of relevant experience in stem cell therapy, bioreactor cell production, scale up, regenerative medicine, tissue engineering with a BA/BS Degree or 3+ years of relevant experience in stem cell therapy, bioreactor cell production, scale up, regenerative medicine, tissue engineering with a Master's Degree or 1+ years of relevant experience in stem cell therapy, bioreactor cell production, scale up, regenerative medicine, tissue engineering with a PhDStrong background in cellular process development and/or mid-scale cell production (2-10L)Technical expertise in cell bioreactor culture, preferably Sartorius Ambr/B-DCU systems and/or vertical wheel bioreactors with scales up to 10L+Proficient with appropriate word processing, spreadsheet, presentation, and related standard softwareExperience with laboratory instrumentation and data softwareExcellent written and oral communication skillsStrong organizational skills and attention to detailAbility to accommodate a non-traditional work schedule (e.g. Sun-Thu, Tue-Sat) and/or contribute to Weekend/Holiday work as neededPrevious industry experience Preferred Qualifications Experience with automated cell processing equipment, such as CliniMACS Plus, LOVO, Cue, Sepax, Sefia, RoteaKnowledgeable in the transfer of R&D cell expansion methods to GMPExperience with relevant statistical software (GraphPad Prism, MODDE, SIMCA, JMP, etc.)" It seems after Minimum Requirements they list "Previous industry experience Preferred Qualifications" then the Preferred Qualifications list. Thus Minimum Requirements ends before "Previous industry experience Preferred Qualifications". So Minimum Requirements includes up to "Ability to accommodate a non-traditional work schedule...". Then "Previous industry experience" is a Preferred Qualification? Actually it says "Previous industry experience Preferred Qualifications". Could be a bullet: "Previous industry experience" under Preferred Qualifications. We'll treat that as part of Preferred Qualifications. Thus Minimum Requirements bullets: list the items before that. Let's extract Minimum Requirements bullet list: - Bachelor’s Degree in biomedical science, cell biology or related field OR Master’s Degree in biomedical science, cell biology or related field OR Doctor of Philosophy (PhD) in biomedical science, cell biology or related field - 5+ years of relevant experience in stem cell therapy, bioreactor cell production, scale up, regenerative medicine, tissue engineering with a BA/BS Degree OR 3+ years of relevant experience ... with a Master's Degree OR 1+ years of relevant experience ... with a PhD - Strong background in cellular process development and/or mid-scale cell production (2-10L) - Technical expertise in cell bioreactor culture, preferably Sartorius Ambr/B-DCU systems and/or vertical wheel bioreactors with scales up to 10L+ - Proficient with appropriate word processing, spreadsheet, presentation, and related standard software - Experience with laboratory instrumentation and data software - Excellent written and oral communication skills - Strong organizational skills and attention to detail - Ability to accommodate a non-traditional work schedule (e.g. Sun-Thu, Tue-Sat) and/or contribute to Weekend/Holiday work as needed Now Preferred Qualifications: - Previous industry experience - Experience with automated cell processing equipment, such as CliniMACS Plus, LOVO, Cue, Sepax, Sefia, Rotea - Knowledgeable in the transfer of R&D cell expansion methods to GMP - Experience with relevant statistical software (GraphPad Prism, MODDE, SIMCA, JMP, etc.) Now Job Location: "This position is located in our Manchester, NH Lab. Flexible hours are necessary." Benefits: "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" We should keep the link? Probably keep as plain text; it's okay. Now "Who We Are" and "Who You Are" sections: we need to preserve substantive info. Who We Are: description of company, mission, therapies, etc. Who You Are: description of role and mission. Let's extract Who We Are paragraph: "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: "Imagine telling people your work helps create the building blocks for 3D printed organs. At United Therapeutics, that's not science fiction. It's the mission. We're seeking a driven Bioprocess Engineer to help develop and scale robust cell production processes that support some of the most ambitious advances in regenerative medicine today. You'll join a highly collaborative team where innovation is expected, scientific curiosity is celebrated, and your contributions have the potential to change the future of transplant medicine for patients around the world. The Senior Bioprocess Engineer, Cell Production and Process Development (OMG) will be responsible for contributing to the production and supply of primary and iPSC-derived cells, as well as the development, optimization, and scale-up of robust, GMP-compliant manufacturing processes. This role independently leads small-to-medium studies and/or cell production runs, ensuring the consistent delivery of high-quality cellular products for research and clinical applications." Note there is a duplicate sentence later; we already captured responsibilities. Now we need to output HTML. Let's structure:About United Therapeutics
...Who We Are...
Who You Are
...Who You Are...