
1. Active participation on Cleaning Validation team meetings to provide input on projects timeline considerations, activities, escalations and status of assigned tasks.
2. Evaluate and understand cleaning processes.
3. Evaluate paper forms, protocols, process and equipment cleaning instructions to transfer them to new digital platform.
4. Identify opportunity to simplify instructions/documentation prior to transfer them to electronic system.
5. Assess work centers equipment capability and cleaning instructions for improvement purposes.
6. Serve as Subject Matter Expert to develop and implement cleaning protocol and forms in Kneat and Tulip platforms, together with implementation of additional data integrity requirements.
7. Revise and approve cleaning strategy documents.
8. Participate in the revision of the cleaning documentation records related to the manufacturing stages and steps.
9. Lead and/or participate on triage activities to assess change control requirements.
10. Issuance or support on change control generation and revision of standard operating procedure.
11. Issuance change control and present it in Change Control Board to pursue approval of the change.
12. Review documentation associated to cleaning program (cleaning validation master plan, risk assessment, protocols, reports, working instructions, sampling scheme, limit calculations, etc.).
13. Revise equipment cleaning instructions while transferring to new digital platform.
14. Revise SOPs related to cleaning program and requirements.
15. Participate /lead the data integrity assessment and actions for cleaning program.
16. Lead training activities provided to manufacturing operators.
17. Support On Call rotation for cleaning execution activities.
18. 100% dedicated to cleaning validation program

QRC group is a life science firm dedicated to provide services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Our services and solutions include:
Process and Laboratory Investigation
• Corrective and Preventive Action (CAPA)
• Change Control
• Training
• Document Management Control
• QA Laboratory
• Methodology Transfer and Validation
• Instrument Calibration
• Validation and Training in Chromatographic Data Acquisition System
• Cleaning Validation
• Automation Engineering
• Quality Systems