Laboratory Technician I

About the Company

Hyacinth Proteins is advancing the development of agriculturally derived bioactive proteins through novel technology, processes, and equipment innovation. This 'next-gen' technology will position Hyacinth Proteins as a leader in the manufacture of ultra-pure, pharmaceutical-grade bioactive proteins.

Job Description

Hyacinth Proteins seeks a motivated, detail-oriented individual to join our Quality team as a Laboratory Technician I (QC Tech I). The Laboratory Technician I will support analytical testing, data recording, and laboratory operations to ensure the quality, safety, and consistency of products manufactured under current Good Manufacturing Practices (cGMP).

The position requires attention to detail, documentation accuracy, and a commitment to following written procedures and laboratory best practices. The Laboratory Technician I will work closely with manufacturing and QA personnel to ensure all products and materials meet internal and regulatory quality standards.

This position is located in Twin Falls, ID and reports to the Quality Assurance Manager.

Specific Responsibilities Include:

• Perform routine laboratory analyses on raw materials, in-process, and finished products in accordance with approved methods. Coordinate and ship samples as needed for external testing.

• Prepare, label, and document samples, reagents, and solutions in compliance with written procedures.

• Operate, clean, and verify laboratory instruments (balances, pH meters, spectrophotometers, pipettes, etc.).

• Support equipment calibration, verification, and preventative maintenance activities.

• Execute and maintain accurate and legible Test Method Document (TMD) forms and electronic records per Good Documentation Practices (GDP).

• Follow approved Standard Operating Procedures (SOPs) and Test Method Documents (TMDs).

• Document test results and promptly report out-of-specification or abnormal findings to supervision.

• Maintain laboratory sample inventory, retention, and proper storage conditions.

• Participate in environmental monitoring and water testing programs to support overall facility control.

• Support incoming material inspections and sampling for quality testing.

• Follow gowning, safety, and cleanliness requirements for GMP laboratory and ISO Class 7 cleanroom operations.

• Generate and organize Certificates of Analysis (COAs), Safety Data Sheets (SDS), and related documentation.

• Provide analytical data and sample support for investigations, deviations, and change-control activities.

• Participate in laboratory housekeeping and QC inventory management.

• Support validation, qualification, or verification of test methods and equipment when trained.

• Ensure all activities comply with company Quality Policies, procedures, and applicable cGMP regulations.

• Maintain adherence to HACCP, HARPC, and Sanitation Standard Operating Procedures (SSOPs) to ensure all formulations and finished products meet specifications.

• Communicate effectively in written and oral form with Quality Assurance and senior management.

• Perform other duties as assigned by the Quality Assurance Manager.

• Must be able to stand for extended periods, lift up to 60 lbs, and work flexible shifts or days to meet production milestones.

Qualifications

Education and/or Experience

• H.S. diploma or higher required; associate's or bachelor's degree in chemistry, biology, or a related scientific discipline preferred
• 1–3 years of laboratory or manufacturing experience in a GMP, biopharmaceutical, or medical device environment preferred
• Experience with analytical testing techniques such as pH, conductivity, or UV-Vis spectrophotometry; familiarity with laboratory instrumentation including Differential Scanning Calorimetry (DSC), ELISA assays, and basic pipetting techniques.
• Working knowledge of the following compliance processes: Current Good Manufacturing Practice (cGMP), Good Documentation Practices (GDP), Hazard Analysis and Critical Control Points (HACCP), Hazard Analysis & Risk-Based Preventive Controls (HARPC), Food and Drug Administration (FDA), Occupational Safety and Health Administration (OSHA)
• Experience with common laboratory and cleanroom equipment such as balances, pipettes, spectrophotometers, and pH meters
• Strong attention to detail and organizational skills with the ability to accurately document results and follow written procedures
• Ability to work independently or as part of a team in a fast-paced GMP environment
• Strong analytical and problem-solving skills to identify and report nonconformances or deviations in a timely manner

Compensation

Hours

• Full-time with ability to work overtime as needed.

Pay

• TBD hourly rate

Bonus

• A yearly bonus will be developed based on the success of the company as defined by management

Benefits

Paid time off

o 10 days of general use

o Federal Holidays: New Year's Day, Memorial Day, Independence Day, Labor Day, Veterans Day (5 days)

o The week of Thanksgiving (5 week days)

o The last 2 weeks of the calendar year (10 week days), unless otherwise noted

Pay: From $20.00 per hour

Expected hours: 40 per week

Work Location: In person