Steriles Standards Manager
Steriles Standards Manager Closing Date: 6th July 2026 (COB) 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 vaccines 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 lead standards and compliance for sterile manufacturing at a GSK UK site. You will work closely with operations, quality, engineering and supply teams to ensure safe, compliant and reliable sterile production. We value problem solvers who coach others, make clear decisions and drive continuous improvement.
This role offers visible impact, career growth and the chance to unite science, technology and talent to get ahead of disease together. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career.
These responsibilities include some of the following: Define, maintain and continuously improve steriles operational standards, ensuring alignment with regulatory requirements and site/global expectations. Drive consistency across manufacturing areas through standard work, ownership of the management monitoring universe and standardisation of procedures, batch documentation and operational practices.
Establish and maintain governance processes to ensure standards are deployed, understood, consistently applied and reflected in audit and inspection readiness activities. Identify gaps, deviations and variability in ways of working, leading improvements and corrective actions to strengthen control, compliance and operational performance.
Monitor adherence to standards through data review, audits and performance indicators, escalating risks and supporting governance forums where required. Coach operational teams and leaders on standards execution, working with Quality, Engineering, Sterility Assurance and Operations to ensure standards evolve with process or equipment changes.
Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals - Experience in sterile pharmaceutical manufacturing or sterile aseptic processes in a regulated environment. - Solid understanding of Good Manufacturing Practice (GMP) for sterile products and contamination control principles. - Practical experience managing deviations, investigations and CAPA (corrective and preventive actions). - Experience supporting audits and regulatory inspections as part of sterile operations. - Strong interpersonal skills with experience coaching or guiding production and technical teams. - Experience with cleanroom classifications, environmental monitoring and sterility assurance methods.
Preferred Qualification If you have the following characteristics, it would be a plus - Degree or formal qualification in pharmacy, life sciences, engineering or a related discipline. - Knowledge of aseptic process validation, sterilisation methods and media-fill activities. - Experience with manufacturing systems such as MES, SAP or electronic batch records. - Training or experience in continuous improvement methods such as Lean or Six Sigma. - Previous role as Steriles Standards lead, Steriles Manager, or similar within pharmaceutical manufacturing.
Working model This role is on-site at Barnard Castle. You should be prepared to spend significant time at the manufacturing site to lead activities and work directly with operational teams. How to apply If this role speaks to you, please apply.
Tell us briefly how your experience will help deliver safe, high-quality and improving sterile operations. We look forward to hearing from you. Inclusion statement We welcome applicants from all backgrounds. We value inclusion and encourage candidates to apply even if they do not meet every preferred qualification.
Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive.
We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
GSK is an Equal Opportunity Employer. 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.
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