Process Technologist

Glaxosmithkline Consumer Healthcare SA; North East; On-site; GBP 35,000 - 55,000; Full time

Job summary

A global biopharma company in the UK is seeking a Process Technologist to design and develop manufacturing processes for new products. You will focus on process validation, project delivery, and quality compliance, ensuring adherence to safety and regulatory standards. The ideal candidate holds a degree in a related field and has technical experience in pharmaceuticals. This role offers competitive pay and a supportive working environment.

Benefits

Competitive salary

Annual bonus based on company performance

Healthcare and wellbeing programmes

Pension plan membership

Shares and savings programme

Qualifications

• Bachelor’s, Master’s or PhD degree in a relevant field.
• Technical experience in pharmaceuticals or biotechnologies is required.
• Strong knowledge of cGMP and regulatory requirements.

Responsibilities

• Design and develop manufacturing processes for new products.
• Implement process improvements using lean manufacturing.
• Resolve process-related issues using RCA techniques.

Skills

Problem-solving skills

Analytical skills

Effective communication

Teamwork abilities

Education

Bachelor’s, Master’s or PhD degree in Chemistry, Biology, Engineering or related field

Job description

Process Technologist

GSK Barnard Castle is a key secondary manufacturing site with industry 4.0 state‑of‑the‑art equipment to support sustained new product introductions and volume increases. The site contributes revenues of ~2 Bn annually and is a key supplier of GSK’s blockbuster products.

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, a pension plan membership, and shares and savings programme.

Key Responsibilities

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 tech transfer and validation of processes.
Project Delivery: 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.

Required Qualifications & Skills

• Bachelor’s, Master’s or 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).

Application Information

Please include a cover letter, in which you describe how you meet the required competencies, or use your CV to submit the required information. The information you provide will be used to assess your application.

When applying for this role, please use the ‘cover letter’ of the online application or your CV.

Benefits

Competitive salary, annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, shares and savings programme, and more. We also offer an agile working culture and support for flexible arrangements.

Why GSK

GSK is a global biopharma company dedicated to uniting 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 through innovation in specialty medicines, vaccines, and four therapeutic areas: respiratory, immunology, oncology, HIV, and infectious diseases.

Equal Opportunity Employer

GSK is an Equal Opportunity Employer. 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.