Date Posted: 09/01/2026
Hiring Organization: Rose International
Position Number: 506714
Industry: Consumer Goods
Job Title: Quality Lab Support Specialist
Job Location: Reynoldsburg, OH, USA, 43068
Work Model: Hybrid
Work Model Details: Onsite 3 days per week (T, W, Th)
Shift: Normal working hours
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 4
Min Hourly Rate($): 20.00
Max Hourly Rate($): 21.50
Must Have Skills/Attributes: Data Entry, Laboratory, Manufacturing
Experience Desired: Experience in a quality, laboratory, manufacturing or warehouse environment (0-2 yrs); Familiarity with quality systems, product inspections, audits, or sample management (0-2 yrs); Experience using data entry or quality management software. (0-2 yrs); Ability to lift and move product samples and materials as needed. (1+ yrs)
Required Minimum Education: High School Diploma or equivalent
**C2C is not available**
Job Description
***Only qualified Quality Lab Support Specialist candidates located near Reynoldsburg, Ohio to be considered due to the position requiring an on-site presence***
Required Education:
• High school diploma or equivalent.
Required Qualifications:
• Experience in a quality, laboratory, manufacturing, or warehouse environment.
• Familiarity with quality systems, product inspections, audits, or sample management.
• Experience using data entry or quality management software.
• Strong attention to detail and organizational skills.
• Ability to accurately follow procedures and work instructions.
• Basic computer proficiency, including Microsoft Office applications.
• Ability to manage multiple tasks and prioritize work in a fast-paced environment.
• Strong communication and teamwork skills.
Job Overview:
The Lab Support Specialist provides essential operational and administrative support to the Quality team. This role is responsible for executing product audits, maintaining laboratory and product standards, supporting quality investigations, managing product samples and retains, and performing general laboratory coordination activities. The position plays a critical role in ensuring efficient quality operations and timely support of product quality assessments and investigations.
Key Responsibilities:
This position provides critical day-to-day support to the Quality organization, helping ensure products, standards, and quality records are properly managed while enabling timely execution of audits, investigations, and quality-related activities. enabling timely execution of audits, investigations, and quality-related activities.
Audit Support:
• Execute routine product audits in accordance with established procedures.
• Accurately document and enter audit results into quality audit systems and applications.
• Communicate audit findings and support the quality team during investigations and follow-up activities.
Product Processing:
• Process and release products from Quality Management (QM) hold status as directed.
• Review and manage first production samples for evaluation.
• Organize and store retained product samples according to established procedures.
Standards and Reference Material Management:
• Maintain, organize, and store product standards and reference materials.
• Manage Product Design References (PDRs) and ensure appropriate storage and accessibility.
• Monitor inventory and coordinate disposal of expired or obsolete standards as directed.
Quality Investigation Support:
• Assist with product testing, evaluations, and analyses related to quality investigations.
• Document product conditions through photography and visual assessments as requested.
• Support product sorting, rework activities, and containment actions in accordance with quality instructions.
• Assist in gathering data and samples needed for quality assessments and root cause investigations.
• Assist in entering quality notification data into SAP
General Laboratory and Administrative Support:
• Dispose of non-saleable products as directed, including destructive audit samples, tested products, line trial samples, and excess product samples.
• Manage the purge and disposition of retained samples, standards, and PDR materials according to established guidelines.
• Coordinate incoming and outgoing laboratory and quality department mail and shipments.
• Maintain and update data files, logs, databases, and tracking systems as needed.
• Support overall laboratory organization, cleanliness, and inventory management.
Physical Requirements:
• Ability to lift and move product samples and materials as needed.
• Ability to stand, walk, bend, and perform routine laboratory and warehouse activities.
• Ability to handle and organize a high volume of product samples and reference materials.
- **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
Rose International has been great to me. I thank everyone there for all of their hard work; it has not gone unnoticed.
Melody, Consultant
It is a great pleasure being a part of the Rose International Team.
Toni, Consultant
Your team at Rose International is always very helpful and responsive.
Barbara, Consultant
Each time I contacted Rose, I was completely satisfied with the great attention and customer service I received. Each person was extremely knowledgeable and patient with my concerns or questions.
Diana, Consultant
Working for Rose International was the most pleasant assignment I have ever had. They were always on top of situations when necessary, and very helpful. I was very proud to be an employee of Rose International, and would recommend anyone to try to work with them.
Melvon, Consultant
EMPLOYEE COMMENTS