Nombre del sítio: UK - North Ayrshire - Irvine
Fecha de publicación: Sep 6 2024
The Technical function at GSK’s Irvine manufacturing site provides best in class processes to ensure that product inputs are understood and maintained through the product life-cycle (within the wider manufacturing and production operations) across the PSC (Pharma Supply Chain) Site. This entails all elements of the manufacture, testing and supply process.
We are looking for a capable Process Engineer to join our team at the Irvine site.
As a Process Engineer you will provide technical expertise (understanding and capability) and take-part in control improvement projects to support the site manufacturing strategy. You will deliver safe, compliant, and robust process operations, as well as be involved with new product introductions, technology transfers, process design and generating engineering solutions (to drive continuous improvement).
Key Responsibilities:
* Provision of technical expertise in the application of process engineering best practice and process safety (on a variety of key projects across site including new product introduction, global supply, and process capability improvements to the supply chain).
* Being the recognised key point of contact for technical knowledge on specific manufacturing unit operations (for which you are responsible for), including ensuring Critical Process Parameters are identified, understood, monitored, and controlled.
* Provision of process engineering support for Product Lifecycle Management, including input to Technical Risk Assessment (and escalation), development and use of Product Control Strategies (for new and mature products), and Product Performance Monitoring.
* Problem solve Technical issues related to dose/product form (using GPS tools such as RCA).
* Manage process improvement projects (ensuring appropriate technical change control to deliver robust, sustainable solutions).
* Investigate alternative new technologies for plant/equipment efficiency improvements and use technical expertise to influence equipment strategy to meet future site goals.
Please Note that this is a site-based role.
Secondment / FTC: This secondment / Fixed Term Contract (FTC) is expected to last circa 12-months in duration. Please ensure you have spoken with your line-manager to ensure they are supportive of your application (this includes a timely-release from your current responsibilities should you be offered the Secondment).
About You:
This role would suit a self-motivated person who has experience of working in a cross-functional manufacturing environment. You will be resilient and calm under pressure, with strong people skills and a proven ability to influence people to achieve and drive performance. You will have a strong continuous improvement mindset.
About Irvine Site:
Manufacturing at the Irvine site includes antibiotics in the oral form (penicillin). It is advised that you take this into consideration when deciding to apply for this position.
CLOSING DATE for applications: Friday 20th of September 2024 (COB).
Basic Qualifications:
* Relevant Engineering, technical or scientific qualifications. (MEng/ BEng), ideally working towards chartership.
* Experience within a manufacturing context (ideally from a highly-regulated industry).
* Understanding of current Good Manufacturing Practice (cGMP)
Benefits:
GSK offers a range of benefits to its employees, which include, but are not limited to:
* Competitive base Salary
* Annual bonus based on company performance
* Opportunities to partake in on the job training courses
* Opportunities to attend and partake in industry conferences
* Opportunities for support for professional development and chartership (GSK are accredited by IET, IMechE, IChemE and other professional bodies)
* Access to healthcare and wellbeing programmes
* Employee recognition programmes
If you would like to learn more about our company wide benefits and life at GSK we would suggest looking at our webpage Life at GSK | GSK .
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