CSO Technician

CSO Technician

Join a leading biotech team as a CSO Technician and help power the future of clinical trial excellence. [Employer hidden — view at passion-project.co.uk] is seeking a CSO Technician to join a leading biotech/biologics organization. This role involves supporting clinical trial packaging operations in a GMP environment. The position offers two fixed shift patterns for flexibility and requires a hands-on approach to ensure quality and compliance.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Start-up, execute cleaning, and complete clinical trial packaging operations per SOPs.
• Perform primary packaging, including bottle filling of oral dosage forms using various equipment.
• Label and assemble clinical trial supplies using automated labelling and walleting equipment.
• Work independently or as part of a team on equipment or process projects.
• Control and monitor production processes and equipment, troubleshoot issues, and escalate problems as needed.
• Develop and apply knowledge of electronic systems, including SAP.
• Complete electronic batch documentation, equipment logbooks, and other relevant production documentation.
• Adhere to GMP requirements and defined procedures to maintain quality standards.
• Work safely in the packaging environment, understanding personal responsibility for Health, Safety, and the Environment.
• Understand and comply with COSHH procedures.
• Participate in internal audits and continuous process improvement initiatives.

Key Skills and Requirements:

• Typically educated to A-level standard, preferably in sciences or IT-related subjects.
• Strong problem-solving skills and ability to collaborate effectively with colleagues.
• Excellent communication and interpersonal skills.
• Ability to work accurately under deadlines.
• Computer literate with the ability to develop and share knowledge.

Required Knowledge and Experience:

• Experience in a packaging and labelling environment within a GMP setting, preferably in clinical trials.
• Working knowledge of SAP.
• Basic understanding of clinical trial operations.

For more information, please contact Grant Van Schalkwyk.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

[Employer hidden] is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. [Employer hidden] is acting as an Employment Agency in relation to this vacancy.

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