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C&Q Project Manager - US, Philadelphia - 8 Month Contract Do you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced C&Q Project Manager for their Philadelphia based location.   What you'll do: Develop and implement a risk-based C&Q strategy for all GMP (direct impact) and non-GMP (indirect impact) systems and assets, aligned with current industry practices.Provide input across all project phases, including design, construction, operational readiness, and technical operations.Lead and manage a team of approximately 15 C&Q Engineers to deliver scope for facilities, utilities, and process equipment.Oversee the development and execution of C&Q documentation in compliance with internal quality standards, cGMP requirements, and client procedures. What you'll need: Bachelor’s degree in an engineering-related discipline.Extensive experience in Cell and Gene Therapy, Drug Product Biotech, and/or OSD pharmaceutical manufacturing.Strong C&Q experience with a proven track record in cGMP-regulated environments.Experience as C&Q Lead on at least one major Cell and Gene Therapy or Biotech project.Strong planning, organizational, and influencing skills.Excellent written and verbal communication skills. If this role is of interest to you, please apply now!#LI-ZM1

C&Q Project Manager - US, Philadelphia - ContractDo you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced C&Q Project Manager for their Philadelphia based location.   What you'll do: Develop and implement a risk-based C&Q strategy for all GMP (direct impact) and non-GMP (indirect impact) systems and assets, aligned with current industry practices.Provide input across all project phases, including design, construction, operational readiness, and technical operations.Lead and manage a team of approximately 15 C&Q Engineers to deliver scope for facilities, utilities, and process equipment.Oversee the development and execution of C&Q documentation in compliance with internal quality standards, cGMP requirements, and client procedures.Ensure team safety and compliance with site safety protocols. What you'll need: Bachelor’s degree in an engineering-related discipline.Extensive experience in Cell and Gene Therapy, Drug Product Biotech, and/or OSD pharmaceutical manufacturing.Extensive C&Q experience with a proven track record in cGMP-regulated environments.Experience as C&Q Lead on at least one major Cell and Gene Therapy or Biotech project.Strong planning, organizational, and influencing skills.Excellent written and verbal communication skills. If this role is of interest to you, please apply now!#LI-ZM1