Job Details

ID #53071417
Estado Carolina del Norte
Ciudad Durham
Fuente BioFire Diagnostics, LLC.
Showed 2024-12-13
Fecha 2024-12-14
Fecha tope 2025-02-12
Categoría Etcétera
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Manufacturing Maintenance Tech 2 - Night Shift

Carolina del Norte, Durham
Aplica ya

Benefits at bioMerieux: Low-cost medical, dental, and vision benefits starting day one 11 paid holidays 160 hours of paid time off Annual bonus 9.5% 401k company contribution with no vesting period Tuition reimbursement up to $10,000 per calendar year Onsite cafeteria with daily food stipend Position Summary & Responsibilities: The normal working hours for this role are anticipated to be 7:00pm - 7:30am working a 2-2-3 rotation schedule. The Maintenance Technician 2 is responsible for supporting the maintenance operations at our medical device manufacturing facility. This role is crucial in ensuring the reliability and efficient performance of our production equipment through basic maintenance tasks and preventive maintenance activities. Complex issues are escalated to senior team members for guidance on troubleshooting and resolution.

Perform routine preventive maintenance on manufacturing equipment

Assist higher-level technicians in troubleshooting and repairing mechanical and electrical systems

Follow established procedures for maintenance activities and documentation

Adhere to FDA regulations, GMP, ISO standards, and safety protocols

Utilize computerized maintenance management systems for work orders and reporting

Contribute to a culture of continuous improvement and operational excellence

Education, Skills, & Experience:

High School diploma/GED with 2+ years of experience in troubleshooting and repairing mechanical and electrical systems.

Experience working in a cGMP/Regulated environment desired.

Able to read ladder logic and troubleshoot/repair PLC’s, electrical systems, AC/DC drive systems, and mechanical systems desired. Proficient in machining, welding, and fabricating a plus.

Excellent documentation and communication skills (written & verbal).

Strong attention to detail and GMP experience (including knowledge of change control, validation, and commissioning processes) desired.

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