- Do you have a passion for making a positive impact on the environment and the lives of others? As a QESH Coordinator, you will play a vital role in ensuring our operations comply with all relevant regulations and standards. Our client manufactures, distributes, sells and markets some of the world's strongest brands in non-alcoholic beverages. It is a leading Western European marketer, distributor, and producer of bottles and can non-alcoholic refreshment.Do you have a passion for making a positive impact on the environment and the lives of others? As a QESH Coordinator, you will play a vital role in ensuring our operations comply with all relevant regulations and standards. Our client manufactures, distributes, sells and markets some of the world's strongest brands in non-alcoholic beverages. It is a leading Western European marketer, distributor, and producer of bottles and can non-alcoholic refreshment.
- ResponsibilitiesEnsure training documentation is current and accessible.Author and review technical documents, including SOPs, protocols, and reports.Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls.Collaborate across departments, external vendors, and global teams to meet documentation and compliance needs.Lead or support continuous improvement initiatives and operational technology improvements.ResponsibilitiesEnsure training documentation is current and accessible.Author and review technical documents, including SOPs, protocols, and reports.Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls.Collaborate across departments, external vendors, and global teams to meet documentation and compliance needs.Lead or support continuous improvement initiatives and operational technology improvements.
- ResponsibilitiesManage the key Quality Systems for the site (Veeva Vault, LMS).Oversee preparation, approval, and training upload of site documentation (GMP, EHS, operational procedures) in Veeva Vault and LMS.Track site documentation schedule, escalate issues, and support timely resolution.Administer LMS and ensure training documentation is accessible.Coordinate records retention and manage control of all records through the Records Management process/tooResponsibilitiesManage the key Quality Systems for the site (Veeva Vault, LMS).Oversee preparation, approval, and training upload of site documentation (GMP, EHS, operational procedures) in Veeva Vault and LMS.Track site documentation schedule, escalate issues, and support timely resolution.Administer LMS and ensure training documentation is accessible.Coordinate records retention and manage control of all records through the Records Management process/too
- Senior QC ScientistInitial 12 month contract - view for extension and/or permanent role.Harwell, OxfordshireUp to £40000 annual salaryOur client is a leading pharmaceutical organisation who are currently recruiting for a Senior QC Scientist based in Harwell, to join the team and help set up the lab and shape the building of a microlab this year.Duties:Perform and oversee routine analytical chemistry & stability testingPerform HPLC (AEX) and NaOH plate readSenior QC ScientistInitial 12 month contract - view for extension and/or permanent role.Harwell, OxfordshireUp to £40000 annual salaryOur client is a leading pharmaceutical organisation who are currently recruiting for a Senior QC Scientist based in Harwell, to join the team and help set up the lab and shape the building of a microlab this year.Duties:Perform and oversee routine analytical chemistry & stability testingPerform HPLC (AEX) and NaOH plate read
