At a Glance
- Tasks: Support clinical safety and ensure high-quality packaging and labelling of trial materials.
- Company: Join a leading global biopharmaceutical organisation making a difference in healthcare.
- Benefits: Gain valuable experience in a dynamic field with opportunities for growth.
- Why this job: Be part of a team that impacts patient safety and clinical trials.
- Qualifications: Background in life sciences or engineering; attention to detail is key.
- Other info: Training provided on clinical safety standards and GMP environments.
The predicted salary is between 36000 - 60000 £ per year.
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
CSO Technician - Packaging & Labelling employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CSO Technician - Packaging & Labelling
✨Tip Number 1
Network like a pro! Reach out to people in the biopharmaceutical field, especially those working in clinical safety or packaging. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical safety standards like DCB0129 and DCB0160. We want you to show off your understanding of these standards and how they relate to the role!
✨Tip Number 3
Don’t forget to highlight your attention to detail during interviews. Share examples from your past experiences where your meticulous nature made a difference, especially in GMP environments or documentation tasks.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace CSO Technician - Packaging & Labelling
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the CSO Technician role. Highlight any relevant background in life sciences, healthcare, or GMP environments to catch our eye!
Show Off Your Attention to Detail: Since this role involves a lot of documentation and compliance, it’s crucial to demonstrate your attention to detail. Use clear formatting and check for typos – we love a polished application!
Express Your Interest in Clinical Safety: Let us know why you’re passionate about clinical safety and risk management. Share any experiences or projects that showcase your interest in these areas, as it’ll help us see your enthusiasm for the role.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Stuff
Make sure you brush up on clinical safety standards like DCB0129 and DCB0160. Familiarise yourself with GMP documentation processes and be ready to discuss how your background in life sciences or healthcare relates to the role.
✨Show Off Your Attention to Detail
Since this role requires strong documentation skills, prepare examples that showcase your attention to detail. Think about times when your meticulous nature helped prevent issues or improved processes in previous roles.
✨Be Ready to Collaborate
This position involves working with various teams, so be prepared to talk about your experience in collaborative environments. Share specific instances where you successfully worked with digital, engineering, or regulatory teams to achieve a common goal.
✨Troubleshooting Skills Matter
Expect questions about how you handle production and equipment issues. Prepare to discuss any relevant experiences where you identified problems and escalated safety concerns effectively, demonstrating your proactive approach to risk management.