Responsibilities
Streamline chemical processes for better efficiency and consistency. Ensure full compliance with GMP and FDA standards, maintaining accurate documentation. Lead process improvement initiatives, collaborating across R&D, production, and QA teams. Provide technical support for scale-up activities, from lab to pilot or commercial-scale operations. Prioritise safety and sustainability, conducting audits and driving adherence to regulations.
About you You will have a degree in Chemical Engineering or a related field; GMP certifications a bonus. You will be skilled in process design, simulation software, and industrial scale-ups with a strong analytical mindset, problem-solving abilities, and strong communication.
What's on offer 36-hour workweek (Monday-Friday). Opportunity to contribute to global pharmaceutical innovation.
Unfortunately, we are unable to provide sponsorship for this role so please only apply if you have the right to work in the UK. #J-18808-Ljbffr