Production Tech 1

Production Technician I – URGENTLY HIRING

A family-owned company, bioMérieux has grown to become a world leader in the field of in vitro diagnostics. For almost 60 years and across the world, we have imagined and developed innovative diagnostics solutions to improve public health. Today, our teams are spread across 44 countries and serve 160 countries with the support of a large distribution network. This includes our SLC site, formerly known as BioFire Diagnostics.

As a valued team member, you will enjoy:

• $1,200 sign on bonus ($600 on the first paycheck and $600 after 6 months of employment)
• 11 paid holidays
• 160 hours of paid time off
• 9.5% 401k retirement match
• Low-cost medical insurance that starts on day one
• Tuition reimbursement up to $8,000/annually
• Onsite cafeteria with daily food stipend
• Annual bonus

Salary & Schedule:

• $17.00- 19.00/hr, based upon experience
• Available Shifts:
  • 1st: Monday – Friday, 6:00am – 2:00pm (no differential)
  • 2nd: Monday – Friday, 2:00pm – 10:00pm (10% shift differential)
  • 3rd:  Sunday – Thursday, 10:00pm – 6:30am (15% shift differential

Position Summary:

The Production Technician I position is responsible for the operation of high speed equipment used in the production and packaging of VITEK 2 cards in a cGMP compliant manner. The position may perform or assist in the setup, operation, inspection, maintenance, troubleshooting and cleaning of equipment used throughout the VITEK 2 Card Manufacturing and Packaging processes.  Additionally, this individual will be responsible for completing production batches and corresponding documentation for the associated tasks, AQL inspections, reworks and material reconciliation that goes along with the batch.  Contribute to building a positive work environment. 

Primary Duties:

• Execute production activities per approved Manufacturing Directions while maintaining compliance with all job-related SOPs.   
• Ensure that all batch paperwork is completed in an accurate, thorough, and timely manner. 
• Execute validation protocols associated with manufacturing/packaging equipment and procedures including revalidation as required to maintain systems in a validated state. 
• Provides assistance with the review and revision of Manufacturing Directions and SOPs necessary for the manufacture and packaging of product.  
• Certified in operation of at least one high speed manufacturing equipment efficiently and effectively, in some cases highly automated, using HMI/SCADA interfaces. 
• Engage in cage movement, maintain product segregation, retrieve and organize raw materials, and ability to learn fork truck operation. 
• Follow appropriate departmental cleaning procedures to ensure adequate cleaning of the manufacturing areas.  
• Setup high speed manufacturing equipment, within defined tolerances, to ensure product runs are started on time and within established guidelines. 
• Always comply with all safety policies and procedures. 
• Appropriately use PPE (Personal Protection Equipment) as required to perform routine and non-routine duties. 
• Maintain all work areas in a well-organized, clean and tidy manner at all times in compliance with cGMP requirements.   
• Perform other duties as assigned by Management. 

Position Requirements:

• High School Diploma or GED
• 1-2 years’ experience in FDA regulated manufacturing environment and GMP is desired
• Ability to express ideas clearly (verbal and written) with the ability to work from verbal and/or written instructions, manuals, work orders and specifications
• Ability to perform necessary calculations and complex task sequencesin order tomeet production requirements
• Attention to detail and the ability to accurately interpret technical documentation are critical
• Ability to perform computer applications including learning and performing SAP transactions
• Ability to routinely lift 20-50 pounds
• Ability to stand for 8-12 hours
• Ability to work overtime as required to cover a 24/7 operation