Process Technologist in Barnard Castle

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, contributing 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 practices with our Performance with Choice programme.

As a Process Technologist, you will work as part of a team supporting the production area providing a technical service. This will involve provision of a New Production Introduction, troubleshooting, working on technical projects & supply of technical data. Your role will span work undertaken in the production environment. All work must be conducted in compliance with specified GMP and EHS standards.

In this role you will…

• Process Design, Development and Improvement: Design and develop manufacturing processes for new products and optimise existing processes to improve efficiency and quality in line with regulatory requirements. Identify and implement process improvements using lean manufacturing, Six Sigma, and other methodologies to increase productivity and reduce waste.
• Process Validation: Input into the specification for new process technologies to enhance production capabilities. Work with R&D and global functions for the tech transfer and validation of processes.
• Project Delivery: Be able to manage a number of priorities and work in an agile way to deliver project milestones.
• Operational Support: Diagnose and resolve process-related issues using root cause analysis (RCA) techniques to minimise downtime and ensure smooth production operations. Collect and analyse process data to monitor performance, identify trends, and drive data-driven decision-making.
• Quality Compliance: Lead or assist in FMEAs, risk assessments, deviations, change controls, and corrective and preventive action closures.
• Safety Compliance: Ensure all manufacturing processes adhere to safety regulations and company policies to maintain a safe working environment.

Basic Qualifications & Skills:

• Bachelors/Masters/PHD degree in Chemistry, Biology, Engineering or another related field.
• Technical or industry experience within pharmaceuticals or biotechnologies.
• Excellent problem-solving and analytical skills.
• Effective communication and teamwork abilities.
• Familiarity with cGMP, industry standards and regulatory requirements.

Preferred Qualifications & Skills:

• Strong knowledge of lean manufacturing, Six Sigma, and other process improvement methodologies.
• Strong project management and self-organisation skills.

Closing Date for Applications: 19th January 2026 (COB)

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.

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.