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You are purpose driven. Growth minded. Ready to stretch your potential. That’s the spirit of the community you will find at Orbia: where the purpose to advance life around the world drives our global team of over 23,000 every single day. From creating solutions to deliver clean water, secure food supplies and reliable information to steering material advances that power the future of green and smart cities, transportation, and healthcare, we never settle for “good enough” when there’s an opportunity to make life better. Where purpose comes to life, it changes lives. This is what we live for. Orbia Fluor and Energy Materials, an Orbia business, is looking for a Process Engineer to be based in Runcorn, Cheshire, UK. Main Purpose Provide process engineering support across the site (80% Medical / 20% Site) supporting both the medical and non-medical operating areas by delivering work related to day-to-day technical support of the operating assets, troubleshooting/root cause analysis, projects & modifications, process engineering, improvements and optimization, investigations/deviations, and audits. Function as part of the Technical Team for the operating areas, working closely with the Technical Plant Managers and with other functions to ensure safe, reliable, efficient and cGMP compliant operation of the assets to achieve the overall business objectives. Main Responsibilities • Demonstrate full personal and professional commitment to SHEQ&S and proactively support the management team in continuously complying with and improving SHEQ&S systems and processes., • Support the Operations Team and Site, effectively managing and resolving technical issues related to plant and unit operation. This includes day to day as well as medium to longer term technical issues or improvements., • Effectively coordinate with internal and external stakeholders on technical and engineering problems to facilitate safe, dependable, and efficient operation of their assets., • Participate in training and development activities related to the operating team and develop, perform, and support training, competence management and human-factors-related activities as required by the management team., • Develop, optimise, and produce required technical and managerial reports on time and to the right quality. Present these reports and associated investigation to internal management teams and customers as and when required., • Conduct conceptual, front-end, or detailed process engineering for assigned projects and modifications to ensure compliance with statutory requirement, recognised good practice and relevant national or corporate standards. Effectively manage assigned projects from concept to implementation including outsourcing when required., • Support and Deputise for the Technical Plant Managers to effectively coordinate and manage systems related to safety, operability, costs, or risk management such as but not limited to alarms, SIS, reliability, RCA, VPCs/unit usages, OEE etc., • Support and when required lead investigation of deviations, identifying corrective and preventative actions, checking for effectiveness, and meeting associated deadlines., • Contribute to the upkeep of the SHEQ and cGMP document library by collaborating with key stakeholders and reviewing documents in a timely manner., • Support customer and regulatory audits. Qualifications Degree in Chemical or Process Engineering. Knowledge/ Experience Required You will ideally have: • At least 2 years’ experience within the chemicals or process industry in a technical capacity, • Experience working on or supporting operating chemical assets., • A history of delivering projects or modifications, taking ideas from concept through to execution., • Experience developing technical proposals, reports, and documentation, including investigations and root cause analysis., • The ability to work effectively within a multi‑disciplinary team, balancing individual contribution with collaboration. In addition, you may also bring: • Understanding of process or chemical engineering principles and unit operations., • Experience with Process Safety Management systems and techniques, such as HAZOP, Management of Change, pre‑start‑up safety reviews, alarm management, SIS, and DSEAR., • Strong technical report writing skills., • Experience in root cause analysis and investigation methodologies., • Knowledge of continuous improvement / LEAN principles., • Experience or knowledge of cGMP and/or COMAH would be an advantage. Behaviours that can help you succeed at Orbia: • Develop yourself & Others, • Foster Collaboration & Inclusion, • Drive Results, • Provide Vision & Direction We welcome purpose-driven dreamers, doers, and builders, recognizing that it takes difference to make a difference. If you’re ready to bring your skills, talents, and perspective to moving your career, the company, people, and the planet forward, we’d like to hear from you. We believe that every voice matters; every community deserves respect; and every challenge is an opportunity and united by empathy, we are stronger for our different perspectives. We are dedicated to building a more diverse, inclusive, and equitable workplace that supports the needs of all our employees regardless of their role, location, identity, and background.

You are purpose driven. Growth minded. Ready to stretch your potential. That’s the spirit of the community you will find at Orbia: where the purpose to advance life around the world drives our global team of over 23,000 every single day. From creating solutions to deliver clean water, secure food supplies and reliable information to steering material advances that power the future of green and smart cities, transportation, and healthcare, we never settle for “good enough” when there’s an opportunity to make life better. Where purpose comes to life, it changes lives. This is what we live for. Fluor and Energy Materials, an Orbia business, is looking for a Stability Analyst (18-month FTC) to be based at The Heath, Runcorn, Cheshire, UK. Main Purpose To manage and oversee Stability trials within the Medical Propellants Quality Control laboratory. To compile regulatory evidence for compliance of stability of medical products manufactured by Orbia. Main Responsibilities • To follow stability master schedule to coordinate on-going and new stability trials for all Medical propellants., • Completing stability reports according to defined timelines., • To raise, report and complete investigations or deviations covering stability studies., • Oversee the maintenance of stability chambers holding stability studies within the medical propellants laboratory., • To support analytical and quality control activities where required. Qualifications • A-Levels essential., • NVQ or above would be desirable. Knowledge/ Experience Required • Experience of working in a QC Laboratory, preferably one working to cGMP standards., • Knowledge and experience in GC analysis., • Experience in stability testing and report writing., • Understanding of stability trials and their role in pharma., • High attention to detail. Behaviours that can help you succeed at Orbia: • Develop yourself & Others, • Foster Collaboration & Inclusion, • Drive Results, • Provide Vision & Direction We welcome purpose-driven dreamers, doers, and builders, recognizing that it takes difference to make a difference. If you’re ready to bring your skills, talents, and perspective to moving your career, the company, people, and the planet forward, we’d like to hear from you. We believe that every voice matters; every community deserves respect; and every challenge is an opportunity and united by empathy, we are stronger for our different perspectives. We are dedicated to building a more diverse, inclusive, and equitable workplace that supports the needs of all our employees regardless of their role, location, identity, and background.

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Extensive medical writing experience within a medical communications agency or an in house pharma med comms team, demonstrating:. Champions best practice among the medical writing team and works closely with senior leadership to continuously evolve and improve our service offering. Langland, a Publi

Extensive medical writing experience within a medical communications agency or an in house pharma med comms team, demonstrating:. Champions best practice among the medical writing team and works closely with senior leadership to continuously evolve and improve our service offering. Langland, a Publi

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Promotional and medical congress booths. No Medical Affairs or Publications.

As a Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve.You'll assist with daily living, providing support and companionship and sharing great moments and memories too.It's a chance to bring your dedicatio

I’m currently supporting a growing medical communications agency on a search for an experienced Senior Medical Writer or Principal Medical Writer to join their scientific team. Senior Medical Writer / Principal Medical Writer. Remote or Hybrid UK | Medical Communications.

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Previous medical writing experience within a CRO, HEOR consultancy, or med comms environment. Hiring: Medical Writer – HEOR & Publications. I’m currently supporting a CRO looking to add an experienced Medical Writer to their growing HEOR and Value Communications team.

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The Senior Medical Writer will be an integral member of our growing medical writing group and will take on a client-facing, collaborative role with direct engagement alongside medical monitors and senior leadership. The role offers meaningful visibility within the organization and requires someone w

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