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About the Role
The Quality Technician is responsible for ensuring products meet all cGMP and Product Specification criteria by reviewing in-process test data and batch documentation in real-time.
Responsibilities
- Conducts approval of pre-start-up activities including line/room clearance, and initial equipment checks.
- Consistently reviews in-process batch documentation to ensure real-time compliance with product specifications, good documentation practices, company SOP’s and cGMP’s.
- Discusses errors and reviews production logbooks for accuracy and compliance.
- Collects data and supports release of batch records.
- Responsible for conducting duties in compliance with safety rules, applicable SOPs, and cGMP guidelines.
- Conduct regular quality line audits of in-process and finished goods against pre-defined characteristics to ensure that all process and product requirements have been satisfied.
- Document audit results on the appropriate QA paperwork making notes about out-of-spec conditions found or other observations of interest.
- Perform Leak Test on in-process material to ensure that product meets intended performance requirements.
- Perform Lot Code validations.
- Perform Control Weight validations at a determined frequency.
- Monitor the performance of metal detection equipment, as applicable.
- Investigate production-related QA problems and make recommendations.
- Visual verification of raw material and packaging material to validate material is in spec to artwork and functionality requirements and is used for its intended purpose on the correct product.
- Execute the plant non-conforming materials procedure when out-of-specification conditions are observed.
- Help individuals performing activities affecting Fit and Function of the product to understand why something is not right when process and/or product nonconformance’s are identified.
- Notify supervisor of unusual problems, delays, and/or safety issues.
- May be asked to support Production on a temporary basis during periods of reduced plant activity.
- Performs other duties as assigned by Quality Management.
Requirements
- High School Diploma or General Education Degree (GED) required.
- Working knowledge of Microsoft Word, Excel, and Outlook is preferred.
- Fluent in English and Spanish desired.
- High attention to detail required.
- Basic understanding of measurement concepts, including length, width, height, and weight.
- Experience in a manufacturing environment, including exposure to quality operations.
- Ability and willingness to follow directions.
- Must be able to communicate, respond to verbal and written instructions in English.
- Ability to effectively troubleshoot problems and recognize when to escalate issues to manager.
- Adheres to company policies and procedures and maintains reliable attendance.
- Ability to lift, carry, push, or pull up to 40 lbs.
- Frequent standing, walking, bending, stooping, and reaching throughout the shift in a manufacturing, packaging, and warehouse environment.
- Regular use of hands, wrists, and arms requiring fine motor skills and manual dexterity.
- Ability to work in varying temperature conditions and around warehouse equipment and machinery.
- Ability to remain on feet for extended periods of time.
Skills
- Quality Assurance
- cGMP
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Troubleshooting
- Communication
Location
- Chicago, IL
Work Type
- Hybrid
- Full-time
Experience Level
- Entry Level
Education Level
- High School Diploma or GED
Salary/Compensations
- $20.00 per hour
Benefits
- Hands-on experience in production packing and quality inspection
- Foundational skills for growth in manufacturing and quality assurance
About the Company
- Radienz Living is a leading North American manufacturer of home and personal care products.
- Provides customers with private-label solutions and contract manufacturing services.
- Committed to agility, innovation, trust and reliability, and sustainable creation.
- Focuses on Unit Dose products and Personal Care Wipes.
- Operates with robust quality systems, multiple GMP certifications, and in-house labs.
- Has FDA/EPA-certified microbiology, quality control, chemistry, and R&D facilities.
Equal Opportunity
- Radienz Living is an equal employment opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status or any other characteristic protected by applicable law.
- We welcome you to inform us confidentially if you may require any special accommodation to participate fully in our recruitment experience. Contact us at 631-952-0100 Ext. 3045
- This position is not eligible for Visa Sponsorship.