Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Operations
: Label Print and Production Supervisor
: None
: Execute Label Print requests and label and package materials for use in clinical trials.
:
1. To print and issue labels and / or leaflets according to requirements in the labelling and packaging works orders or print requests.
2. To ensure all blank or pre-printed labels, leaflets and code breakers for clinical trial use are stored and identified correctly.
3. To liaise with label suppliers to obtain quotes.
4. To prepare purchase orders for ordering labels.
5. Maintain Label stock on ERP system.
6. Maintain the cleanliness of the Labelling room.
7. To follow labelling and assembly instructions in line with company requirements and external regulations.
8. To complete assembly documentation in line with company requirements and external regulations.
9. To maintain equipment used for packing operations, as required.
10. To maintain the cleanliness of the packing rooms.
11. Comply with the companies Health and Safety standards.
12. Where required, undertake tasks and projects outside the job holder’s area of responsibility.
:
13. Correct labels are produced in compliance with cGMP, regulation and in line with clients’ instructions.
14. Materials are packed to the appropriate quality standards.
15. All documentation is completed to the appropriate company standards.
16. All labelling and packing operations are completed to the appropriate company standards.
17. All equipment is maintained to the appropriate standard.
18. GCSE Grade C and above (or equivalent) in English and Mathematics.
19. Previous experience using printing software & in a packaging or manufacturing environment is desirable.
:
20. Exceptional attention to detail and code verification.
21. Excellent time management and organisational skills.
22. Proficient in the use MS Office Packages and ERP systems.
23. Great written and verbal communication skills.
24. An understanding of Quality Standards including GMP, GDP and Good Documentation Practice.
Join us and be part of building the bridge between life changing therapies and patients.