Be the hands ensuring every clinical pack meets the highest standards.
Proclinical is seeking a UK_CSO Technician to join a team in UK. This role focuses on supporting clinical trial packaging operations in a GMP environment. You will play a key role in ensuring quality standards are met while contributing to process improvements and maintaining a safe working environment.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
1. Execute cleaning and clinical trial packaging operations following Standard Operating Procedures.
2. Perform primary packaging tasks, including bottle filling of oral dosage forms using various equipment.
3. Label and assemble clinical trial supplies using automated labelling and walleting equipment.
4. Work independently or collaboratively on equipment or process-related projects.
5. Monitor and control production processes and equipment, troubleshoot issues, and escalate problems as needed.
6. Develop and utilize knowledge of electronic systems, such as SAP.
7. Complete electronic batch documentation, equipment logbooks, and other relevant production records.
8. Adhere to GMP requirements and quality standards in the packaging environment.
9. Maintain a safe working environment, understanding personal responsibility for Health, Safety, and Environmental principles.
10. Comply with COSHH procedures and participate in internal audits.
11. Contribute to continuous process improvement initiatives.
Key Skills and Requirements:
12. Educational background at A-level standard, preferably in sciences or IT-related subjects.
13. Strong problem-solving skills and ability to collaborate effectively with colleagues.
14. Excellent communication and interpersonal skills.
15. Ability to work accurately and meet deadlines.
16. Proficiency in computer systems and willingness to develop and share knowledge.
17. Experience in a GMP packaging and labelling environment, ideally within clinical trials.
18. Familiarity with SAP and basic knowledge of clinical trial operations.