Job Description
CLEANING SUPPORT SPECIALIST required by CareerWise Recruitment for our pharmaceutical client in Co. Tipperary. Initial 12 month contract on offer, this role is fulltime onsite for the first 6 months for training purposes, after that this will be a hybrid role. The CLEANING SUPPORT SPECIALIST will be responsible for management and tracking of Cleaning validation parameters and commitments along with issuing and management of cleaning changes and documentation.
Role of this position
1. Responsible for issuing and management of cleaning changes and documentation.
2. Responsible for reviewing and incorporating relevant updates as communicated via the Technical Team Lead.
3. Responsible for management and tracking of Cleaning validation parameters and commitments.
4. Support for Cleaning Investigations
5. Compilation of CPV reports, CAR, and APRs
6. Ownership and management of changes.
7. Generation and tracking of cleaning campaign documentation.
8. Stewardship of validated campaign data.
9. Liaising with product teams to align turnaround targets.
10. Investigation support for Cleaning QNs.
11. Assessments of OOTs.
12. Support project assignments as required.
13. Completion of validation reports.
JOB REQUIREMENTS
14. Degree qualification in a science or engineering-related discipline.
15. Knowledge of GMP standards.
16. Good communication skills, both written and verbal.
17. Strong technical writing skills.
18. Previous experience in API or Drug Product manufacturing is desirable.
19. To maintain accurate records in compliance with GMP expectations.
20. To understand and internalise procedures relevant to GMP operations.
21. To communicate clearly and concisely on technical issues.