Direct message the job poster from CPi Biotech
Marketing & Business Development Manager / CPi Biotech & CPi Technology
Company Description
CPi Biotech, a leading manufacturer of Single Use assemblies and Bioprocess skids for the Biopharmaceutical market, combines experienced design engineers and a dedicated cleanroom production team to deliver world-class single use technologies. Our products, ranging from simple jumper sets to complex assemblies with bags, pumps, and instrumentation, are manufactured in a state-of-the-art EN ISO 14644 Class 7 cleanroom facility. We emphasize personal involvement, responsiveness, and reliability in daily interactions, striving for lifelong partnerships with our valued customers.
Role Description
This is a full-time on-site role for a Cleanroom Operator located in Cork. The Cleanroom Operator will be responsible for assembling single-use technologies, maintaining cleanroom standards, following detailed work instructions, and ensuring the quality and integrity of the products. Daily tasks include handling and inspecting components, operating cleanroom equipment, and documenting the production process.
Qualifications
1. Perform all administrative functions as required by the job, adhering to and implementing company QUALITY Procedures and systems in everyday activities and tasks that are necessary to progress the works/job at hand
2. Follow detailed assembly instructions, processes, and procedures to correctly assemble medical devices
3. Comply with policies, guidelines, and any regulatory requirements of the company's Quality System
4. Report problems with quality, processes, equipment, or materials to the Operations Lead / Quality Lead
5. Perform manual assembly and visual inspection of Single Use Technologies
6. Complete line clearance, Batch records, training records, and other documentation as required
7. Complete routine tasks with minimal supervision
8. Maintain a clean and organized work area to facilitate manufacturing functions
9. Work in a cleanroom environment following GMP Guidelines and defined Gowning procedures
10. Ensure compliance with the requirements of the Quality Management System in relation to Policies, Procedures, Work Instructions etc.
11. Ensure compliance with the requirements of the Occupational Health and Safety Management System
12. Other duties as assigned by the Management team
We’re looking for team players who enjoy a fast-paced and progressive environment and the opportunity to join a dynamic company.
Closing date for applications is Friday, 9th May 2025.
Seniority Level
Entry level
Employment Type
Full-time
Job Function
Management and Manufacturing
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