QA Lead

Innovative Labs • Springville, UT

8h

About The Position

The Quality Assurance Lead performs a variety of working level and technical duties as needed to assure the ongoing compliance with quality standards and specifications in an assigned work unit, including but not limited to the laboratory, documentation, production floor, shipping receiving and outbound inspection.

Requirements

• The ability read, speak and understand basic English
• Must possess oral / written communication skills, ability to manage multiple priorities
• Follow GMP standards and guidelines
• Understand and apply information set forth in SOP’s
• Handle confidential information
• Ability to cross train in areas within the quality department.
• High School Diploma or GED
• 5+ years related experience
• Pass skills assessment exam with 70% or higher on both reading and math comprehension

Responsibilities

• Able to work well with others.
• Must be able to maintain a positive environment and inspire team members to work together.
• Audit production lines to verify that GMP standards, guidelines and procedures are being followed.
• Be able to create, master production records.
• Review Manufacturing records for correct information, proper editing and completeness.
• Monitor all area clearances, cleaning verifications, in process inspections, finished product AQL's, in-process machine operations including the monitoring of weights, temperatures, etc.
• Provide support to production to maintain a quality products and identify areas of improvement.
• Verify that the product is labeled and dispositioning properly.
• Release all finished goods.
• Implement process improvement.
• Test lab equipment and basic lab test, PH, Brix, Wa, organoleptics.
• Help maintain and establish critical control levels.
• Ensure customer specifications are met.
• Work with production to initiate alerts for any non-conforming products or processes.
• Review non-compliances with the quality management team.
• Provide training as needed.
• Assist in updating, implementing, maintaining and reporting any deviations in SOP and cGMP practices.
• Ensure all personnel follow SOP and cGMP guidelines, help train, and report discrepancies to management.
• Generate reports and maintain databases tracking quality issues and information.
• Other duties as assigned.

Benefits

• Comprehensive health, dental, and vision coverage—plus a few weeks of paid parental leave when it matters most.
• Paid time off and holidays to help you unwind and recharge
• Real opportunities to grow your skills and make an impact as we evolve
• A collaborative team that’s adaptable, supportive, and driven to succeed together

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED