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We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021.

We continue to modernise, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together.

Barnard Castle MSAT Process Technologist – 18-month contract (end 2024)

• Depending on the successful applicant, this role may be offered as an internal secondment or fixed term contract.

GSK Barnard Castle is one of the most complex sites globally in the GSK network. This is a great opportunity for an enthusiastic, driven, hardworking, team player to join an established & successful technology team.

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 laboratory, Pilot Plant & production environments. All work must be conducted in compliance with specified GMP and EHS standards.

In This Role:

• Comply with all GMP guidelines and all Regulatory requirements, ensuring all documentation is of a standard acceptable to external inspectors (e.g. MHRA/ FDA).
• Have a direct line report to the relevant Team Lead & provide regular updates on all matters regarding the project(s) you are responsible for.
• Support Technology Transfer for respective Sterile products from R&D to GSC, including all aspects of product industrialisation
• Spearhead cross functional teams either for a small project or sub-projects.
• Understand GPS / Lean principles and with support be able to use the tools and techniques as required.
• Demonstrate agile thinking and manage and deliver multiple technical priorities
• Act as a point contact and provide an effective troubleshooting service for the specific production areas of the Product Stream that have been allocated as the responsibility of the Technologist.
• Manage problem solving and root cause analyses
• All production, QA, Engineering, and operational planning staff working to be kept informed of identity of the troubleshooting point contact and the role being performed and any subsequent changes.
• Undertake self-audits on a regular basis, to ensure implementation of the required technical and GMP standards is uniform throughout.

Our Global Supply Chain (GSC) business is responsible for making and supplying our pharmaceutical and biopharmaceutical products around the globe. The GSC organisation is involved with every production stage from the infrastructure of the manufacturing sites, supply forecasting, regulatory inspections, and the product’s quality.

To be successful in this role it is imperative that you demonstrate an ability to drive common objective thinking, with a complete focus on providing solutions. You will need to be persuasive, have a strong continuous improvement mindset, work with meticulous attention to detail and have proven experience dealing with diverse internal and external stakeholder groups. You will also have worked in a highly regulated industry.

Closing Date for Applications: 15th February 2023

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.

During your application, you will be requested to complete voluntary information which will be used in monitoring the effectiveness of our equality and diversity policies. Your information will be treated as confidential and will not be used in any part of the selection process. If you require a reasonable adjustment to the application / selection process to enable you to demonstrate your ability to perform the job requirements, please contact 0808 234 4391. This will help us to understand any modifications we may need to make to support you throughout our selection process.

• LI-GSK

Why you?

Basic Qualifications

We are looking for professionals with these required skills to achieve our goals:

• An enthusiastic approach to pharmaceutical process development and the ability to effectively communicate, both written and verbal, in a clear and accurate manner.
• Knowledge in Unit Operations associated with the API/product and understands the impact of material changes on manufacturability.
• Knowledge of the structured problem-solving approaches used for all product & process issues.

Preferred Qualifications/ Experience

If you have the following characteristics, it would be a plus:

• Pharmaceutical experience in a technical, manufacturing or quality function
• Relevant degree or equivalent
• Industrial experience in a Technical, Science or Engineering discipline covering range of processing formats applicable to Pharmaceutical / Medical Device / Healthcare / FMCG.

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class*(*US only).

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 [email protected] or 0808 234 4391. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels

As you apply, we will ask you to share some personal information which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.

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