Are you a Process Operator looking for a new contractual / ongoing position?
Acorn by Synerige is currently recruiting on behalf of our client for skilled and motivated Process Operators to join the organisation in various departments.
The ideal candidate will possess a strong mechanical background and have substantial experience in process and plant operations.
The Recruitment Co. is urgently recruiting an Office Administrator to join our clients team based in the Gorseinon area.
With over 70 years experience in the gas industry, our client requires an Office Administrator to assist and support the Sales and Service departments covering a wide range of tasks and administrative duties.
Main Duties
Assisting the Sales Department and Service Department in administration functions.
Working as part of a team you will be working in a dynamic, fast paced environment where no two days are the same.
We are looking for someone with a real can-do attitude who is passionate about delivering excellent customer service and willing to go the extra mile for our customers.
Are you an experienced Senior Quality Engineer with a passion for driving quality excellence across production, packaging, assembly, and warehouse activities?
This is a hands-on role where you'll collaborate closely with Production, Engineering, and Warehouse teams to maintain and enhance our quality systems.
If so, we have a fantastic opportunity for you to join our dynamic team at our factory site in Swansea.
You will assist in new product and test equipment development, through testing prototypes and component parts, verifying their function and performance.
Just Life Sciences are recruiting for an Innovative and global leading business who are growing rapidly and are seeking a Development Engineer to join their R&D department.
You will provide a global evaluation of all investigations commissioned and executed, acting as the crucial link between investigators and research personnel.
As a Study Monitor, you will play a pivotal role in overseeing the progress of clinical and application research trials.
You will ensure that all studies are conducted, recorded, and reported in compliance with protocols, SOPs, ICH-GCP, and applicable regulatory requirements.