Device Technologist - 12 Month Secondment

Site Name: UK - County Durham - Barnard Castle

Posted Date: Apr

Device and Packaging Technologist (MSAT)

Location: Barnard Castle (Site-based)
Contract Type: 12 month FTC/ secondment

Closing Date: 4th May 2026 (COB)

Business Introduction

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.

Role Purpose

The Device and Packaging Technologist is responsible for delivering technical support and expertise across device assembly and packaging activities at the Barnard Castle site and associated external supply sites. This includes supporting New Product Introduction (NPI), change control, technical issue resolution, and continuous improvement for sterile, intranasal, dermatological, and device-combination pharmaceutical products.

The role acts as a key technical interface between site teams (production, engineering, quality, technical, logistics, planning), central technology teams (Device Technology and Artwork Packaging Services), and external suppliers, ensuring compliant, robust, and efficient device and packaging solutions throughout the product lifecycle.

In this role you will

• Provide first-line technical support for device assembly and packaging operations, including issue resolution, root cause analysis, and support to deviations, CAPAs, complaints, and audits.
• Support New Product Introduction, technical transfer, and change control activities, ensuring compliant and robust implementation for devices and packaging.
• Act as a technical interface between site teams, central device and packaging technology functions, and external suppliers.
• Lead and support line trials, validation, qualification, and process/equipment readiness in line with GMP and regulatory requirements.
• Drive continuous improvement in process capability, efficiency, Cost of Goods, and Cost of Waste across device and packaging operations.
• Ensure effective specification, documentation, and lifecycle management of device components and packaging materials, maintaining full compliance and inspection readiness.

Basic Qualifications & Skills

• HNC with relevant industry experience or Degree-level qualification in Engineering, Science, or a related discipline.
• Proven experience in a technical manufacturing environment, covering device assembly and/or packaging in Pharmaceutical, Medical Device, Healthcare, or FMCG sectors.
• Proficient in the use of digital tools to communicate, report, and analyse technical and process data.
• Good understanding of Health, Safety & Environmental requirements.
• Working knowledge of supplier management and the external supply base.
• Competent understanding of validation methodologies.

Preferred Qualifications & Skills

• Strong understanding of device and packaging development processes, including global standards and end to end lifecycle management.
• Knowledge of packaging materials, forming and finishing processes, packing lines, suppliers, specifications, documentation, and SPC/qualification.
• Understanding of materials and manufacturing methods for moulded components, including polymers, pigments, and injection moulding techniques.
• Good appreciation of pharmaceutical GMP, regulatory expectations, inspection readiness, and medical device regulations (e.g. CE marking, FDA guidance).
• Understanding of pharmaceutical development activities, including R&D, New Product Introduction, and Technology Transfer.
• Experience managing specifications, drawings, metrology, and testing systems, with the ability to work collaboratively across functions and apply effective project management and stakeholder influence.

Equal Opportunity Employer Statement

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.

Contact for adjustments

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call.

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CMS Disclosure

For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at .