Engineering Automation Lead

Site Name: UK – County Durham – Barnard Castle Posted Date: Nov 28 2024 Engineering Automation Lead We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 2.3 billion packs of medicines and doses of vaccines in 2023. We continue to modernise, so we can launch even more new products at speed whilst continuing to deliver across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions, and artificial intelligence to deliver for patients. The Engineering Automation Lead will provide strategic input and direction to enable the site to meet its business goals by effectively balancing the management of day-to-day operations with long-term strategic planning. This involves ensuring that advanced instrumentation, automation, and control engineering techniques are implemented across the Barnard Castle Site in a GMP compliant manner to meet both local and global requirements. By integrating robust management practices with strategic initiatives, the site can optimize operational efficiency, maintain regulatory compliance, and achieve sustainable growth. Key Responsibilities include, but are not limited to: Develop and implement a comprehensive operations automation strategy that aligns with the site’s business goals and objectives. Team Leadership: Manage and mentor a team of automation engineers and build capability and skills with maintenance technicians, fostering a collaborative and innovative work environment. System Design and Implementation: Lead the design, development, and implementation of advanced automation systems, including PLCs, SCADA, and DCS. GMP Compliance: Ensure all automation systems and processes comply with Good Manufacturing Practices (GMP) and regulatory requirements. Training and Development: Develop and deliver training programs to ensure staff are proficient in the use of automation technologies and best practices. Continuous Improvement: Drive continuous improvement initiatives by staying current with emerging automation technologies and industry trends and integrating them into the site’s operations where applicable. Technical Support: Provide technical support and troubleshooting for automation systems to minimize downtime and ensure smooth operations. Provide subject matter expertise to regulatory inspections and interact with auditors as necessary. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Degree in a Science/ Engineering related discipline such as Automation, Control, Electrical or Mechatronic. Six Sigma and Lean Manufacturing experience gained from the pharmaceutical industry.; Black Belt or Green Belt desirable. Technical expertise in several scientific and engineering automation areas including ISA standards (e.g. S88, S95), P&ID nomenclature, Automation architecture, instrumentation and electrical wiring diagrams, communication networks, control panels, HMI, MES, SCADA, PLC and Historians. Broad and in-depth knowledge with practical experience of computer and application validation (preferably using GAMP methodology), cGMPs, and 21 CFR Part 11 in an FDA regulated environment. Proven Leadership Skills in a cGMP environment gained from hands-on programming and troubleshooting for Automation, Instrumentation and IT systems. Ability to interface with operational and senior management within the organization. Experience gained designing and programming automation applications. May include both firmware and software development. Preferred Skills If you have the following characteristics, it would be a plus: MEng / MSc in a Science or Engineering related discipline such as Automation, Control, Electrical or Mechatronic. A sound scientific and engineering understanding of pharmaceutical secondary processing. Good knowledge of IT architecture management, data warehousing, virtualization & implementation processes Practical knowledge of Cybersecurity within an OT space. Demonstrated project management skills. Working knowledge and understanding of EHS Practices and regulations with respect to the installation of automated plant. A good appreciation of FDA PAT initiatives and the impact on the Pharma industry. Proven track record in providing automation support and maintenance for instrumentation, automation and controls. Closing Date for Applications: Friday 6th December 2024 (EOD) Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). 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