Process Engineer - Life Sciences

Overview As a Process Engineer at LJC Design & Engineering, you will shape the planning and design of life sciences manufacturing facilities. You will translate manufacturing processes into clear design inputs, working with clients, process architects, and multidisciplinary teams to deliver compliant, efficient layouts. You’ll contribute to front-end planning, capacity analysis, and regulatory-aligned design solutions in fast-paced projects. This role offers the opportunity to impact facilities that support regulated production across multiple modalities. You will collaborate across engineering, architecture, and construction to drive integrated outcomes. Compensation / BenefitsDiscretionary annual bonusMedical, dental, and vision plans401kgenerous PTO and paid holidaysemployee assistance programlearning & development programs ResponsibilitiesLead or support process definition and design for life sciences facilities from planning to construction supportDefine process flows, unit operations, equipment needs, and space requirements for regulated manufacturingDevelop process narratives, block flow diagrams, and equipment layouts that inform architectural and engineering designCollaborate with clients to understand manufacturing objectives, capacity, product mix, and constraintsTranslate process requirements into compliant, efficient, and flexible facility layouts with process architects and project teamsCoordinate with utilities, mechanical, electrical, automation, and architectural teams to align process needs with systems and infrastructureSupport front-end proposals, technical narratives, and early planning conceptsParticipate in client meetings and planning sessions related to process definition and capacity planningEnsure compliance with GMP/GxP and industry guidelinesReview design deliverables for alignment with process requirements and project objectivesParticipate in multidisciplinary coordination reviews to resolve design challengesStay current with emerging technologies and best practices in life sciences modalities Key requirements10+ years of life sciences manufacturing process engineering experienceBachelor’s degree in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, or related fieldExperience with at least one major modality (e.g., mAbs, aseptic fill–finish, ATMPs, mRNA, vaccines, API, OSD)Strong understanding of regulated manufacturing processes and unit operationsExperience translating process requirements into facility design inputs and layoutsFamiliarity with GMP/GxP environments and regulatory expectationsExperience in design-build or fast-track project delivery environments (preferred)Strong communication and collaboration across engineering, architectural, and construction teamsProfessional Engineer (PE) licensure preferred but not requiredstrong communication skillsclient-facing technical discussion abilitycross-functional collaborationprocess definition and designblock flow diagrams and process narrativesequipment layouts and space planning