SSE, a CWS group company with over 20 years' experience, is an award-winning company that specializes in Cleanroom services, contract cleaning, facilities services, and facilities audits. At SSE, we operate within the Life Sciences Sectors, providing Cleanroom Cleaning & Contamination Control to Medical Device, Pharma, Software & Call Centre Facilities.
We ensure all our colleagues are fully trained to ISO9001:2015, ensuring that all our customers receive the best quality services.
We are currently recruiting for a number of full-time Cleaning Technicians to join our team. This is a great opportunity to join an expanding company with excellent opportunities to progress your career. The ideal candidates will have 1-2 years of experience in a similar role. We require all candidates to have a good understanding of written and oral English.
Start date: Immediately - Shift work Days/Evenings/Nights. Must be flexible.
Responsibilities include, but are not limited to, the following:
1. Comply with competencies and standards held by SSE.
2. Generate and execute cleaning validation protocols, plans, and reports as required.
3. All technicians are required to carry out duties on a daily basis as per Client Specification / SOP.
4. Perform sterilization and maintenance checks.
5. Use chemicals specified on the specification/SOP for each individual job.
6. Measure all chemicals as per manufacturers/SOP recommendations.
7. Ensure Safety Data Sheets are present on site for employees to read and be familiar with.
8. Wear PPE where applicable.
9. Report any incidents/accidents to your supervisor/manager.
10. Participate in RAMs where required.
11. Keep all equipment designated to each area within that area (i.e. Cleanroom).
12. Adhere to company health and safety regulations.
13. Participate in training and development activities provided by SSE.
14. Comply with the requirements of the quality management system ensuring adherence to ISO standards.
15. Maintain a safe and clean work environment by following current good manufacturing practices (cGMP) and standard operating procedures; complying with legal regulations; monitoring the environment.
16. Ensure the Quality Policy is understood and applied within your role.
17. Assist with training of new employees.
18. Follow current good manufacturing practices (cGMP).
19. Assist with the investigation and resolution of quality deviations raised within the Manufacturing Department.
20. Ensure a high standard of cleanliness is maintained.
21. Update job knowledge by participating in training opportunities. Training is carried out on an ongoing basis.
22. Enhance organizational reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.
Authority includes, but is not limited to, the following:
1. Review and complete Logbooks in accordance with cGMP standards and compliant with written procedures.
Requirements:
1. You must have your leaving certificate or higher for this role.
2. Be able to work 12-hour shifts from both 6 am to 6 pm and 6 pm to 6 am.
3. Have excellent written and spoken English.
4. It may be necessary to work alternative hours, shift patterns, or unsociable hours including weekends from time to time.
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