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Device Engineer

5651306

Barnard Castle, England

1 day ago

43264 - 60000 GBP

GSK

www.gsk.com

Brentford, United Kingdom

Emma Walmsley

$10+ billion (USD)

Company - Public

1830


Job Description

Site Name: UK - County Durham - Barnard Castle
Posted Date: May 12 2023


CLOSING DATE:
Sunday 4th June

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, and as a key supplier of some of GSK’s blockbuster products, the site contributes revenues of ~$2Bn annually.

We are addressing gender equality at all levels within our organisation, we also remain committed to improving ethnic diversity within GSK and recruiting and developing talent that mirrors the communities in which we work. With support from our Global Disability Council and our employee resource group, the Disability Confidence Network, we are working hard to create an inclusive workplace.

We want GSK to be somewhere everyone can feel a sense of belonging and thrive. Our success absolutely depends on our people.

As a Device Engineer you will be a technical expert for device assembly and functionality for both legacy and New Product Introduction (NPI projects on behalf of Manufacturing, Science & Technology (MSAT) throughout the entire GSK network, with most aligned assets sitting within the GSK Barnard Castle site currently. While providing first touch troubleshooting and advice on technical projects, you will also be embedded in the production environment, ensuring critical process parameters are defined and controlled.

In this role you will…

  • Be responsible for being the technical head on a manufacturing unit operations ensuring Critical Process Parameters are identified, understood, monitored, and controlled. Where applicable, liaise with process measurement technology (PMT) experts to understand the relationship between measurement, impact of variability in raw materials and intermediates, environmental conditions, equipment conditions, manual operations, and their integration with the control strategy.
  • Represent technical in the Operations management team, working closely with engineering, production, and quality to deliver the production requirements. Ensure day to day technical issues are urgently resolved.
  • Spearhead and/or support design transfer activities to internal and external manufacturing sites. Provide technical support as a Drug-device Combination (DDC) product Subject Matter Expert (SME) to multi-functional teams for process development, technology transfer, and life cycle management of combination products.
  • Maintain a strong level of validated understanding and proficiencies within life cycle management, including expertise in design controls, manufacturing technologies and upcoming combination products for commercialisation
  • Be responsible for delivering key technical activities including NPI trials and planned change implementation.
  • Support design and development work in support of equipment selection, installation, and validation (including business process change) and support the standardisation of manufacturing and process measurement technology (e.g., PAT) on site.

Why you?

Qualifications & Skills:

  • Bachelors/Honours degree, or equivalent in an appropriate scientific or engineering discipline (or relevant experience and actively working towards).
  • Area of Specialisation: Production engineering, medical device assembly and function, device design and component quality attributes.
  • Industrial experience in a Technical, Science or Engineering discipline covering range of processing formats applicable to Pharmaceutical / Medical Device / Healthcare / FMCG.

Preferred Qualifications & Skills:

  • Knowledge of device/assembly manufacturing processes and Drug Device Combinations in general.
  • Knowledge of the structured problem-solving approaches used for all product & process issues. Some awareness of global packaging technologies and the interface with device technologies.

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 positively impact the health of 2.5 billion people by the end of 2030.

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 Ukdiversity.recruitment@gsk.com 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.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.


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