• Perform studies of internal or external hazards in accordance with applicable reference standards • Conduct safety functional analyses • Produce accident studies and probabilistic safety analyses (PSA) • Write chapters/sections of the safety report • Perform impact analyses of modifications on safety assessments • Coordinate hazard-related activities

• Serve as an Engineer on electric transmission line design projects for high-voltage (HV) and extra high-voltage (EHV) systems • Apply NESC, ASCE, ACI and other applicable standards in engineering and design • Perform engineering analyses, prepare bidding documents, draft plans and specifications, and prepare material procurement and construction documents • Work with a multi-person Leidos team and interface with clients, project planning, environmental, permitting, and construction management personnel

• Design, configure, and deploy Azure infrastructure components • Build and manage hybrid and cloud-native systems using Infrastructure as Code (IaC) tools • Implement automated deployment and configuration pipelines • Support cloud modernization and migration initiatives • Configure and manage Windows and Linux servers across cloud and on-premises environments • Monitor system performance to ensure high availability, uptime, and security • Develop detailed migration roadmaps and execution plans • Actively participate in Agile ceremonies and collaborate within cross-functional delivery teams • Communicate effectively with clients and represent the Professional Services organization

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description This position may be performed remotely, but requires the flexibility and willingness to travel as needed. Praxis is seeking a skilled and hands-on Process Engineer to serve as Praxis’s lead point of contact with our Contract Manufacturing Organizations (CMOs). You’ll work onsite at partner facilities to validate small molecule API manufacturing processes, ensure successful tech transfer, and support commercial readiness. You’ll also play a key role in maintaining reliable supply by overseeing future production. The ideal candidate combines strong technical fundamentals with clear, proactive communication, and thrives in a fast-moving, cross-functional environment. Primary Responsibilities - Ability to understand written chemical synthesis processes from lab partners and help translate those to instructions for industrialized execution by authoring scale up spreadsheets and process manuals. - Efficient use of technologies and applications to gather, analyze and archive large data packages that can support regulatory filings. - Review relevant documentation from CMOs and lab partners including instructions, procedures, batch records, non-conformances, in-process controls, bulletin of analysis, developmental reports. - Work alongside Quality Assurance to ensure all proper regulations and standards are followed in all our processes being executed by third parties. - Adhere to industry guidelines, standards and laws including being well-versed in cGMPs. - Travel required - PIP at CMOs (US and worldwide). Qualifications - Advanced degree in chemical engineering or other relevant engineering field; MS or equivalent a plus. - Pharmaceutical or fine chemical industry experience required. - 8 years’ with a BS degree or 6 years’ with an MS degree of applied experience in CMO management, chemical manufacturing, or comparable positions that handle diverse chemical syntheses in laboratory and manufacturing environments, reviewing Manufacturing and Executed Batch records, operating procedures, non-conformances, change controls, and fostering business partner relationships. - Excellent written and visual communication skills with an ability to build relationships internally and externally. - Self-motivated and able to contribute to a productive and collaborative team environment. - Highly organized and detail-oriented with a passion to deliver quality results. - The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions. Benefits - 99% of the premium paid for medical, dental and vision plans. - Company-paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. - Dollar-for-dollar match up to 6% on eligible 401(k) contributions. - Long-term stock incentives and ESPP. - Discretionary quarterly bonus. - Extremely flexible wellness benefit. - Generous PTO, paid holidays and company-wide shutdowns. - Joining a phenomenal crew of colleagues who are smart, engaged and inspiring. Company Description Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members. Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.