Apply today, work tomorrow, and get paid weekly! Want a great work environment? We're hiring now for a Quality Assurance in Twin Falls, ID.

Seeking highly independent, entrepreneurial individuals who will assist in developing a commercialization-focused, industrial-scale production operation supported by novel protein research.

The Cleanroom Production Technician I will join a growing team in this early-stage company to apply expertise in technical production of dairy-derived proteins. They will support the Quality Assurance department with the readiness and operation of the Hyacinth Proteins production facility.

The position involves assisting in cleanroom operations, ensuring adherence to established processes and procedures, and contributing to the overall quality of the products. The role requires attention to detail and a commitment to following precise cleanroom procedures to guarantee the efficacy and safety of pharmaceutical products.

The position is located in Twin Falls, ID but may also assist with operations in Jerome, ID and will report to the Vice President of Protein Manufacturing.

• Weekly pay of $20.00 per hour

• Direct deposit & debit card payment options

• Health, vision, dental, life, and disability insurance

• Get weekends off

• Weekly Pay

• Perform the setup, operation, and sanitation of all production facilities and related manufacturing equipment

• Operate, maintain, and troubleshoot process equipment utilized in the facility, and perform equipment adjustments as needed

• Perform precise measurements to accurately add chemicals, buffers or reagents during processing

• Pass and maintain gowning qualification to perform Gowning Requirement for ISO Class 7 Clean room operations

• Responsible for accurately maintaining accurate records, required logs, books, and other procedures to comply with regulatory requirements

• Interface with QA/QC/Material departments during the course of work to coordinate inspections and efficient flow of subassemblies and completed product

• Enter and record production activities in appropriate quality systems

• Responsible for handling, decontamination, and cleaning of production supplies, instruments, and equipment to support all cleanroom production related activities

• Responsible for reporting all discrepancies to the Quality Assurance Manager

• Support department and plant Safety goals by continuously demonstrating safe behavior

• Maintain a clean and orderly work area

• Ability to work flexible shifts, and flexible days within the week to meet batch milestone requirements

• Perform other manufacturing activities as assigned by the VP of Protein Manufacturing

• May use lyophilizers, fluid bed dryers, autoclaves, vacuum pumps, pH meters, thermometers, balances (scales), water bath circulators, sonicators, mixers, centrifuge, blenders, air gun, temperature recorders, refrigerators, freezers, pallet jacks, electrical equipment, analytical equipment, cleaning chemicals, acids and bases and related cleanroom production equipment

• While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, and write/type

• The employee must be able to stand for 8 hours, or more as needed and lift up to 50lbs

• Manage and complete all required documentation related to production (Batch Record, Logs and Forms)

• Assure that all facilities are adherent to Hazard Analysis Critical Control Point (HACCP), Hazard Analysis & Risk-based Preventive Controls (HARPC), Sanitation Standard Operating Procedures (SSOPs), formulations, & finished product consistently meet specifications

• Ability to communicate effectively in written and oral form with Quality Assurance staff and other team members

• Must be able perform the essential job functions of this position with or without reasonable accommodation

• Day Shift, 8:00 am to 5:00 pm

• Monday - Friday

• H.S. or higher with experience in nutraceutical, medical device or pharmaceutical cleanroom manufacturing preferred

• 5 years experience, preferably in a biopharmaceutical setting

• Experience with the following compliance processes:

  • Hazard Analys