QA Inspector (Night Shift) at Innovative Labs

Springville, Utah, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Jun, 26

Salary

0.0

Posted On

14 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP Standards, Auditing, Record Review, AQL Inspection, In-Process Checks, Material Review, Alert Initiation, Investigation, SOP Adherence, Communication Skills, Priority Management, Cross Training, Reading Comprehension, Math Comprehension

Industry

Food Production

Description

Description About Innovative Labs We are a leading maker of liquid dietary supplements, known for our innovation, strong R&D, and focus on quality. With our in-house team, we create custom liquid products for top wellness, nutraceutical, and food brands. At Innovative Labs, we believe in teamwork and creativity. For over 15 years, we’ve helped brands bring new ideas to life with high-quality liquids, gels, purees, pastes, oils, and emulsions. Our modern facilities and dedicated team work together to make products that matter. Here, you’ll grow, learn, and be part of a team that’s always improving and moving forward. Why You’ll Love Working Here: Your Work Matters: Support the Brands People Use Every Day Collaborate & Create: Join a team that values fresh ideas, open communication, and teamwork Grow Your Career: We encourage curiosity, learning, and stepping up to new challenges Supportive Culture: Thrive in a workplace that values your contributions and well-being About the Position: The Quality Assurance Inspector works to guarantee that procedures and standards at Innovative Labs are being executed in the correct manner. Working alongside the production team, this role maintains and works to improve our production processes and ensures that guidelines are being met. What You’ll Do: Audit production lines to verify that GMP standards, guidelines and procedures are being followed and met. Review Manufacturing records (MBR) for appropriate information, corrections, proper editing and completeness Monitor all area clearances, cleaning logs, in-process AQL’s, In-Process checks, temperatures, weights, burst, brix, pH are complete and accurate Provide support to production to help achieve their production goals and maintain a quality product and identify areas of improvement Ensure personnel follow SOP and GMP guidelines Collect product retains and lab samples AQL inspect finished product Initiate Material Reviews and make disposition decisions Review and audit batching/blending records for completeness and analytical tests meet specifications Alert Initiation and Investigation-work with production to initiate Alerts for any non-conforming products or processes. Investigates any alerts. Initiate Material Reviews Perform other duties and functions as assigned by management Other duties as assigned What Makes You a Great Fit 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 2 or more areas within the Quality Pass skills assessment exam with 70% or higher on both reading and math comprehension High School Diploma or GED 2+ years of related experience The Perks of Joining Our Team 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 Ready to innovate with us? Apply now and let’s build the future together!

Responsibilities

The Quality Assurance Inspector ensures that all procedures and standards are correctly executed by auditing production lines for GMP compliance and reviewing manufacturing records for accuracy and completeness. This role also involves supporting production goals, identifying areas for improvement, collecting samples, and initiating investigations for any non-conforming products or processes.