About LJC The Role We Want You For The Life Sciences Project Architect plays a critical role in translating client operational and technical requirements into compliant, efficient, and constructible facility designs. Lead the architectural design and technical execution of life sciences manufacturing projects, including pharmaceutical and biotechnology facilities.Translate client operational workflows, regulatory requirements, and technical criteria into effective architectural solutions for highly regulated environments.Provide architectural expertise in programming, feasibility studies, facility planning, cleanroom design, process adjacencies, and material and personnel flows.Support and guide architectural teams through all phases of design, including programming, planning, feasibility, concept development, schematic design, design development, construction documentation, and construction administration.Collaborate closely with multidisciplinary teams, including project managers, process architects, lab planners, engineers, and construction partners, to deliver coordinated design solutions.Ensure architectural designs comply with applicable codes, standards, and regulatory requirements, including cGMP, FDA, EU pharmaceutical regulations, and ISO 14644 cleanroom standards.Review and approve architectural drawings, details, and specifications to ensure technical accuracy, constructability, and alignment with project requirements.Support project managers in maintaining design schedules, managing scope, and addressing coordination issues as they arise.Participate in client meetings, design reviews, and technical presentations, supporting clear communication and client confidence.Conduct regular quality checks on architectural deliverables to maintain high standards of design and documentation.Mentor and support junior architectural staff, fostering technical growth, collaboration, and professional development.Stay current with life sciences industry trends, regulatory developments, and best practices in facility design. Minimum of 7+ years of architectural experience, with a strong focus on life sciences manufacturing, pharmaceutical, biotechnology, or other regulated facility types.Bachelor’s or Master’s degree in Architecture from an accredited institution.Registered Architect with an active professional license (required).Demonstrated experience delivering architectural design for regulated environments, including cleanrooms and controlled manufacturing spaces.Strong understanding of life sciences regulatory requirements, including cGMP, FDA, EU pharmaceutical guidelines, and ISO cleanroom standards.Proficiency in AutoCAD, Revit, and related architectural design and documentation tools.Solid technical and coordination skills, with the ability to work effectively within multidisciplinary design teams.Strong written and verbal communication skills, including participation in client-facing discussions and presentations.Ability to manage multiple priorities and support complex projects in a fast-paced environment.Proven ability to mentor junior staff and contribute positively to a collaborative team culture.
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