Your vision is ambitious. Just like ours.

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Explore your tasks and responsibilities

• Develops facility concepts around operational and business goals for manufacturing assets in the Life Science Industry
• Develops feasibility and concept studies that meet globally recognized regulatory guidelines for GMP
• Develops feasibility and concept studies that meet Client guidelines as defined in Tender documents
• Conducts reviews of facility risks and facilitate implementation of facility planning approaches to mitigate those risks
• Uses specialist knowledge and experience to solve complex tasks around segregation strategy, functional adjacencies, GMP flows, and equipment integration into facility layouts
• Delivers on-the-job knowledge sharing/training/mentoring within technical discipline
• Follows technology trends and maintains knowledge within technical discipline
• Supports development of new methods/tools/ for feasibility and CD execution and improve existing solutions supporting compliant facility planning
• Stays current in global regulations impacting facility attributes for the manufacture of biologics and pharmaceutical drug substance and drug product
• Integrates with other disciplines, both internal and Client resources, to optimize facility solutions
• Supports development of optimized facility standards for global use across the Company
• Ensures use of best practice within recognized Industry facility models
• Participates actively in relevant cross-organizational/cross site standardized solutions specifically for feasibility and conceptual design
• Participates in Industry forums to expand the growth of the Company and our Body of Knowledge
• Attends special courses/practical training in field of expertise
• Other duties as assigned

Show your expertise

• Bachelor’s degree in Architecture required
• 15 years of experience in facility planning and design
• 10 years of consulting experience in biotech/pharmaceuticals
• Experience with multi-product facility design, single-use based manufacturing platforms, advanced therapeutic product facilities
• Experience in the execution (design, build, start-up) of capex projects for drug substance and drug product manufacturing
• Experience and comfort working in/with complex corporate environments
• Recognized expert within process architecture discipline, specific to biologics and pharmaceutical manufacturing
• Versed in global regulatory aspects of GMP related to facility design
• Adept at finding innovative methods and solutions for Customer/project/business requirements
• Fluent in the use of Visio and CAD platforms and other visual tools to present ideas and solutions
Ability to communicate design solutions and use of methods, tools and technology in solutions, to a global audience.

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