Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccine manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. 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. Position Summary You will support on-site production of oral solid dosage (OSD) products. You will work with operators, engineers and quality colleagues to keep production lines safe, compliant and efficient. This role offers clear growth opportunities to build technical skills, lead small improvement projects and contribute to work that helps patients. Operate and monitor OSD packaging lines (Blister and Bottle) to meet production plans, safety and quality targets. Investigate deviations, support root cause analysis, and help implement corrective and preventive actions. Support internal and external audits and help maintain compliance with Good Manufacturing Practice (GMP). Record production data accurately and use SAP or local systems for transactions and reporting. Contribute to continuous improvement projects using practical problem solving and production data.



We are seeking professionals with the following required skills and qualifications to help us achieve our goals: Basic Qualifications University degree or vocational qualification in engineering, pharmacy, chemistry or a related technical field, or equivalent practical experience. At least 2 years' experience in a pharmaceutical or regulated manufacturing environment. Practical knowledge of GMP and quality practices in pharmaceutical industry. Experience working on oral solid dosage packaging lines. Basic user skills in production systems such as SAP or electronic batch records. Experience in deviation investigation, CAPA and structured root cause analysis. Familiarity with automation, process control systems, or industrial digital tools. You will be based at the manufacturing site and work closely with production and engineering teams. Skills Data Integrity Digital Fluency Manufacturing Processes Production Management Project Coordination Quality Compliance Site Operations Spanish We are a general 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. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

📌 Production Technician (España)
🏢 GlaxoSmithKline
📍 España