19/04/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later19/04/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later19/04/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later19/04/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later19/04/2024 | Fulltime | Sheffield | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later19/04/2024 | Fulltime | Merthyr Tydfil | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later19/04/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later19/04/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later10/04/2024 | Fulltime | ITI Group | £35,000 Full-time Glasgow - Hybrid About the Job Working in a team to design, build, test and implement industrial control systems (both hardware and software), utilising Programmable Logic Controllers (PLC's), Human Machine Interfaces (HMIs), Supervisory Control and Data Acquisition (SCADA) software
Save for later10/04/2024 | Fulltime | Sheffield | ITI Group | £35,000 Full-time Sheffield - Hybrid About the Job Working in a team to design, build, test and implement industrial control systems (both hardware and software), utilising Programmable Logic Controllers (PLC's), Human Machine Interfaces (HMIs), Supervisory Control and Data Acquisition (SCADA) software
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