At a Glance
- Tasks: Lead production projects and ensure smooth integration of new technologies in manufacturing.
- Company: Join GSK, a global biopharma leader dedicated to improving health worldwide.
- Benefits: Competitive salary, inclusive culture, and opportunities for career growth.
- Other info: On-site role at Barnard Castle with a collaborative team environment.
- Why this job: Make a real impact on health by innovating in medicines and vaccines.
- Qualifications: Experience in manufacturing or process technology, problem-solving skills, and familiarity with GMP.
The predicted salary is between 45000 - 55000 £ per year.
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.
Provide technical and operational leadership for production-related elements of capital, NPI and project delivery across the Site Sterile Value Stream. Ensure that projects are integrated into live manufacturing safely, compliantly and with minimal disruption to supply. The role focuses on production readiness, operational input into design and validation, and the successful deployment of new equipment, processes and ways of working into routine operations. The role also provides technical leadership for post implementation activities, including fronting project implementation audits where required, developing the technical content and implementation plan for change controls, and supporting the integration and development of digital recipes in partnership with Smart Manufacturing and MES teams.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Act as the operational/production SME for capital, NPI and improvement projects, ensuring manufacturability, compliance and production requirements are embedded from design through implementation.
- Provide production input into project design, URS, risk assessments, FAT, SAT, commissioning and validation activities to ensure alignment with GMP, operational requirements and site ways of working.
- Lead operational readiness for new equipment, processes and changes, including line set-up, process definition, standard work, training, coaching and effective handover into base business.
- Coordinate and support production activity during trials, engineering runs, validations and project execution phases, ensuring safe, compliant delivery and timely resolution of technical issues and deviations.
- Develop, review and govern production documentation and change controls, including SOPs, batch records, risk assessments, implementation documents, technical content and deployment actions.
- Provide project governance updates, escalate production risks and readiness gaps, support post-implementation reviews and audits, and contribute to digital recipe and manufacturing system integration with Smart Manufacturing and MES teams.
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Strong practical experience in packaging, manufacturing or process technology in a regulated environment.
- Hands-on experience running trials, validations or qualifications in a production or packaging setting.
- Strong problem solving using data, with experience in root cause analysis and corrective action implementation.
- Familiarity with Good Manufacturing Practice (GMP) and relevant regulatory expectations.
- Track record of delivering small projects or improvement workstreams using lean or structured problem solving.
If you have the following characteristics, it would be a plus:
- Experience in pharmaceutical or biotechnology packaging or manufacture, including pack design changes, secondary packaging or man/fill systems.
- Experience with Design of Experiments (DoE) and basic statistical analysis.
- Experience creating component drawings, bills of material and technical specifications.
- Experience working in a matrix organisation and collaborating across geographies.
This role is on-site at Barnard Castle. Candidates should be prepared to work from the site and collaborate closely with colleagues on the shop floor.
What success looks like:
- Timely, clear resolution of issues that reduces downtime and waste.
- Smooth product and pack transfers that meet quality expectations.
- Concise, usable technical documentation and validated processes.
- Strong collaboration across production, engineering, quality and supplier partners.
If you are practical, curious and enjoy hands-on problem solving, we want to hear from you. Apply now and tell us in your CV or cover letter how your experience matches the responsibilities and qualifications above. If you need reasonable adjustments during recruitment, please tell us when you apply — we are committed to inclusion and to supporting all applicants.
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. 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.
Operations NPI Technologist in Barnard Castle employer: GlaxoSmithKline
GSK is an exceptional employer, offering a dynamic work environment in Barnard Castle where innovation meets purpose. With a strong commitment to employee growth and development, we provide opportunities for hands-on problem solving and collaboration across diverse teams, all while contributing to the health of millions through our high-quality medicines and vaccines. Our culture prioritises accountability, ambition for patients, and inclusivity, ensuring that every team member can thrive and make a meaningful impact.
StudySmarter Expert Advice🤫
We think this is how you could land Operations NPI Technologist in Barnard Castle
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like GlaxoSmithKline.
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We think you need these skills to ace Operations NPI Technologist in Barnard Castle
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at GlaxoSmithKline!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show GlaxoSmithKline that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at GlaxoSmithKline!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At GlaxoSmithKline, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at GlaxoSmithKline
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at GlaxoSmithKline that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with GlaxoSmithKline’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
