Senior Automation Controls Engineer – Facilities

Introduction to roleThe Senior Automation Controls Engineer – Facilities & Engineering is responsible for leading and managing the technical aspects of facilities and process automation/controls, including development and validation, engineering projects, and capital investments within a pharmaceutical organization. This role involves providing expert technical guidance, overseeing complex projects, and ensuring that all systems and processes meet regulatory requirements and support operational efficiency.AccountabilitiesLead technical teams and provide guidance on facilities and process automation/controls, including development and validation activities, engineering solutions, and capital projects.Mentor and support junior engineers and other technical staff in development of cross functional support for automated systems.Collaborate with cross-functional teams to align engineering and project activities with organizational goals.As asset owner, oversee the maintenance and operation of automation/control systems and equipment within the siteincluding critical facilities/utilities, laboratories, production areas, and administrative spaces.Develop and implement strategies for facility automation/controlsimprovements and upgrades to enhance operational efficiency and compliance.Ensure automation/controlssystems adhere to health, safety, and environmental regulations.Lead the development and execution of validation strategies, protocols, and documentation for site systems, equipment, and processes with focus on assets associated with automation/controls.Ensure that validation activities meet regulatory requirements (, FDA, EMA) and internal standards.Manage complex validation projects, including protocol design, execution, and reporting.Oversee automation/controls programs to ensure the reliability of systems including electrical components, software environments, and automated field devices.Develop and implement maintenance and inspection programs for critical equipment.Ensure automation/controls engineering procedures and processes comply with industry standards and regulatory requirements.Lead engineering projects related to the design, installation, and commissioning of systems and equipment.Ensure engineering activities adhere to Good Manufacturing Practices (GMP) and other relevant regulations.Develop and implement preventive and predictive maintenance programs to enhance equipment reliability.Manage all aspects of capital projects, including automation/controls systems upgrades, expansions, and new installations.Develop project plans, budgets, and schedules; monitor progress and ensure projects are completed on time and within budget.Coordinate with internal stakeholders, external contractors, and vendors to achieve project objectives and compliance.Prepare and review comprehensive documentation for qualification/validation, engineering procedures and work instructions, and capital projects.Generate detailed reports on project status, validation results, project activities, and asset ownership/maintenance work.Ensure that documentation is accurate, complete, and compliant with regulatory requirements.Ensure all facilities, systems, and processes comply with regulatory requirements and industry standards.Develop and enforce safety protocols and emergency response plans.Conduct regular audits and inspections to ensure compliance and address any issues promptly.Identify and implement process improvements to enhance efficiency, reduce costs, and improve system reliability.Stay current with industry trends, technological advancements, company guidance, and regulatory changes to ensure best practices are applied.Essential Skills/ExperienceBachelor’s degree in Engineering, Electrical Engineering preferred, or a related engineering field; Master’s degree preferred.7-10 years of experience in automation/controls software and equipment systems, with background in qualification/validation, facilities engineering, and capital projects.Significant experience in a pharmaceutical or regulated industry is preferred.Extensive knowledge of GMP, FDA regulations, and other relevant compliance requirements.Proven experience in leading complex automation/controls processes, asset ownership, engineering projects, and capital investments.Strong project management skills with experience in budgeting, scheduling, and resource allocation.Excellent analytical, problem-solving, and communication skills.Ability to manage multiple priorities and work effectively under pressure. Working Conditions:Office and on-site facilities environment, with occasional travel to various company sites or off-site locations.May require occasional evening or weekend work to address urgent issues or project needs.Desirable Skills/ExperienceCell Therapy Experience When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.AstraZeneca is a place where every day brings new challenges. We lead from the front to ensure everyone's voice is heard on site while building trust and respect with our teams. Our adaptable nature allows us to draw on diverse expertise across functions to overcome obstacles. We champion ideas from anyone on our site with a drive to see things through. Our supportive team environment ensures we succeed together by looking out for each other. With opportunities for growth beyond your role in a stable company committed to eliminating emissions by 2025, AstraZeneca is where you can make a real impact.Ready to take on this exciting challenge? Apply nowDate Posted03-Nov-2025Closing Date30-Dec-2025Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.