Waste Operator & Production Aid
Based on workload, the figure supports the cleaning of the production area including classified areas and equipment, and the shipping activities
- Transfers waste material (Radioactive and non-radioactive) to proper storage areas including separate waste collection in the site dedicated areas.
Main responsibilities:
- Issues specific documentation to manage radioactive and non-radioactive waste materials
- Coordinates the pickup and destruction of both Non-hazardous and hazardous waste with waste companies.
- Checks all type of wastes getting out from the production department being sure they are compliant with all applicable laws in particular for radioactivity risks
- Manages the retain sample storage by verifying material, labels and documents for completeness and accuracy
- Ability to operate all applicable radiation detection equipment.
- Promptly report to the Production Manager and/or the HSE Manager any deviation inherent to the assigned activities
- Execute all assigned activities in compliance with internal procedures (HSE, GMP, others) and in compliance with applicable laws and regulations
- Complete applicable required job specific training, cGMP, HS&E, Dangerous Goods, ADR rules, Cleaning etc.
- Participates to related GMP documentation with QA
- Registers according to the specific law the shipment of all type of waste
- Coordinated by the Supervisor or other production key figure supports the preparation of product shipment (e. g.
type A) and the related documentation, supports in maintain safety stocks of gowning and dpi and supports the cleaning of the production area including classified areas and equipment.
**Commitment to Diversity & Inclusion**:
- Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. _
**Minimum requirements
What you will bring to the role:
- High School diploma or equivalent.
- Basic English (write and speaking), fluent Italian
- Preferably 2 years of manufacturing experience in a (Radio-) Pharma regulated industry.
- GMP knowledge.
- Hazardous shipping training.
**Division
Oncology
**Business Unit
ADVANCED ACCELERATOR APPLICATIONS
**Country
Italy
**Work Location
Colleretto Giacosa
**Company/Legal Entity
AAA Italy Srl.
**Functional Area
Technical Operations
**Job Type
Full Time
**Employment Type
Regular
**Shift Work
No
**Early Talent
Yes
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