Inspector

As an Inspector/Packer, you will perform critical quality control, weighing, and packaging for medical-grade plastic components within an FDA-regulated production environment. This role is designed for a detail-oriented professional with a background in final testing or quality control who can ensure every component meets rigorous medical safety standards.

Responsibilities:

In this technical role, you are responsible for the final line of defense in our manufacturing process, ensuring all medical products adhere to strict FDA regulations. You will conduct precise visual inspections under magnification to identify defects, perform manual assembly of small parts using specialized hand tools and fixtures, and manage accurate weigh-counts for finished goods. Beyond the physical handling of product, you will be responsible for maintaining impeccable production records and work order documentation within our inventory management system. Your expertise will ensure that our clean-room environment remains compliant and that all packaged products are labeled and tracked with 100% accuracy.

Working hours: 6:30 AM - 6:30 PM

Skills:

Experience using inventory management systems (ERP/MRP).

Formal training in Quality Assurance or medical device manufacturing.

High-level proficiency in reading and interpreting complex technical procedures.

Education:

High School

Experience:

0-1 years

Qualifications:

Proven QC or Final Test experience within an FDA-regulated production environment.

Technical documentation skills, including the ability to complete production records and work order data with high accuracy.

Strong manual dexterity and hand-eye coordination for assembling small parts and using magnification tools.

Basic computer proficiency in Microsoft Word, Excel, and Outlook.

If you have a keen eye for detail and enjoy working with your hands, this is a great way to enter the medical manufacturing field.

Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

key responsibilities

In this technical role, you are responsible for the final line of defense in our manufacturing process, ensuring all medical products adhere to strict FDA regulations. You will conduct precise visual inspections under magnification to identify defects, perform manual assembly of small parts using specialized hand tools and fixtures, and manage accurate weigh-counts for finished goods. Beyond the physical handling of product, you will be responsible for maintaining impeccable production records and work order documentation within our inventory management system. Your expertise will ensure that our clean-room environment remains compliant and that all packaged products are labeled and tracked with 100% accuracy.

experience 0-1 years

skills Experience using inventory management systems (ERP/MRP).Formal training in Quality Assurance or medical device manufacturing.High-level proficiency in reading and interpreting complex technical procedures.

qualifications

Proven QC or Final Test experience within an FDA-regulated production environment.Technical documentation skills, including the ability to complete production records and work order data with high accuracy.Strong manual dexterity and hand-eye coordination for assembling small parts and using magnification tools.Basic computer proficiency in Microsoft Word, Excel, and Outlook.

education High School