Are you looking to join a leading global biopharmaceutical organisation as a CSO Technician, supporting clinical safety activities and contributing to high‑quality packaging and labelling of clinical trial materials. This role blends digital health safety, documentation, and GMP clinical supplies operations.
Key Responsibilities
* Support compliance with UK clinical safety standards DCB0129/DCB0160 and assist with safety documentation (risk logs, safety cases, incident logs).
* Assist with hazard workshops, safety‑impact assessments, and monitoring system changes for safety risks.
* Complete clinical trial packaging and labelling tasks including bottle filling, automated labelling, assembly, and GMP documentation (batch records, logbooks, SAP entries).
* Troubleshoot production and equipment issues and escalate safety concerns when needed.
* Collaborate with digital, engineering, regulatory, and quality teams to support safe system deployment.
What We’re Looking For
* Background in life sciences, healthcare, engineering, or digital health.
* Strong attention to detail, documentation skills, and interest in clinical risk management.
* Experience with GMP environments or packaging/labelling is an advantage.
* Understanding of clinical safety standards (DCB0129/DCB0160) is beneficial; training available.
For more information please get in touch - jamie.keith@cpl.com