This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Biocomposites is an international medical devices company that engineers, manufactures, and markets world leading products for use in infection management in bone and soft tissue. Based in Keele, UK, it has global operations across Europe, USA, Argentina, Canada, China, and India. Biocomposites is a world leader in the development of innovative calcium compounds and bone cements for surgical use. Its products regenerate bone and target infection risks across a variety of specialties, including musculoskeletal infection, orthopaedics, trauma, spine, foot and ankle, podiatry, and sports injuries. Biocomposites products are now used in over one million procedures per annum and sold in more than 100 countries around the world. Primary Responsibilities as a Manufacturing Process Engineer, you will play a vital role in shaping the success of our Medical Devices products. With your in-depth understanding of Mechanical Engineering, manufacturing processes, and mechanical design, you will lead the way in enabling procurement and localization activities during new product inquiries and the initiation of new programs. Responsible for the methods, system and equipment used in a manufacturing facility to convert raw materials into their final product form. They ensure the smooth operation of factories, plants and production facilities.
Job Responsibility:
Assessing industrial processes and taking measurements and data
Developing practices, routines and solutions to help improve productivity and product quality
Designing and running process simulations, performing risk assessment testing to eliminate time and cost constraints
Preparing process documentation and operating instructions
Overseeing and assessing new and existing processes and workflows
Devising, implementing and testing new strategies to help optimise productivity
Analysing data to discover areas that need improvements and upgrades
Assessing compliance and adherence to safety and quality standards and reporting to higher management about their findings and proposals
Requirements:
Level 5 in appropriate Process Engineering / Design or equivalent
Minimum 5-year experience in Pharma or Medical Device
Proven Knowledge/Skills in Medical Device / Pharma processes and equipment