Description

GSK Barnard Castle is a key secondary manufacturing site and has invested heavily in industry 4.0 state of the art, bespoke equipment to support sustained new product introductions and volume increases, and as a key supplier of some of GSK's blockbuster products, the site contributes revenues of ~$2Bn annually.

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.

We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.

Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK

Process Monitoring Senior Technologist will perform and oversee environmental monitoring, testing and provide technical expertise and oversight in environmental monitoring that supports sterile manufacturing operations.

In this role you will…

• Perform and oversee routine environmental monitoring (viable and non-viable) in sterile manufacturing areas, ensuring compliance with regulatory and internal standards.
• Conduct and coordinate time-critical testing to support production schedules, ensuring minimal operational disruptions.
• Actively support production lines during sterile operations, ensuring compliance with aseptic techniques, cleanroom behaviours, and sterility assurance practices.
• Proactively identify, intervene, and escalate any deviations or incorrect practices in sterile operations to ensure compliance and protect product quality, supporting investigations and preventive actions.
• Support the education and mentoring of operators and production staff on aseptic principles and behaviours, reinforcing a culture of compliance and sterility assurance.
• Ensure accurate and complete documentation of environmental monitoring and testing activities, maintaining compliance with regulatory and internal standards.
• Perform analysis of monitoring data to identify anomalies or risks, escalating findings for further investigation and corrective action.
• Collaborate with production and quality teams to ensure seamless execution of monitoring activities during critical manufacturing operations and provide input for sterility assurance during batch release.
• Support batch release by reviewing and providing environmental monitoring data to assess compliance with sterility requirements.
• Assist with project and routine requalification studies such as smoke pattern evaluations and biological indicator testing to support sterility assurance and manufacturing validation processes.

Why you? 

Basic Qualifications & Skills:

• A-level qualifications (or equivalent). Grade A-C GCSE in Mathematics and English
• Good experience in production and laboratory environments.
• Experience of GMP manufacturing, validation, documentation and laboratory and processes.

Closing Date for Applications: 7th November 2025 (COB)

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 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.

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on UKRecruitment.Adjustments@gsk.com or 0808 234 4391.  The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary.

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive

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