Wknd QC Inspector- Day Shift

SWM International; Windsor (CT); On-site; USD 45,000 - 65,000; Full time

Job summary

Mativ is seeking a QC Inspector to support the Sustainable & Adhesive Solutions function. This role performs in-process and finished-goods inspections, records results, and ensures compliance with product specifications under supervision from Quality Engineering.

You will conduct audits, maintain calibration and lab MRO inventory, assist in training, and contribute to continuous improvement initiatives while following GDP and safety rules in a fast-paced manufacturing environment.

Qualifications

• Minimum of 2 years' experience in QA or QC manufacturing.
• High School diploma required; bachelor's degree highly preferred.
• Familiar with basic measurements, test equipment and basic math skills.
• Medical device industry experience preferred.
• Ability to communicate and work within a team environment.

Responsibilities

• Perform audits and testing of in-process and finished goods to ensure compliance with PRS or Tech 11.
• Record and enter test results into the Scapa ERP System.
• Coordinate shop floor QC testing based on production schedules.
• Issue non-conformance reports for nonconforming materials.
• Maintain and calibrate QC test equipment and reference standards.
• Assist in training new QA inspectors and personnel.

Skills

QA/QC experience

Team collaboration

Basic math skills

Documentation skills

Education

High School diploma

Bachelor's degree preferred

Tools

Scapa ERP System

Test equipment

Calibration tools

Job description

Mativ is a global leader in specialty materials headquartered in Alpharetta, Georgia. The Company offers a wide range of critical components and engineered solutions that connect, protect, and purify our world.

Our QC Inspector supports Mativ's Sustainable & Adhesive Solutions Function. This individual will perform inspections and tests throughout the manufacturing process to ensure compliance with specifications under the supervision of Quality Engineering.

**The shift schedule is Friday - Sunday, 6:00am-6:00pm**

Responsibilities

• Performs all auditing and testing of in-process, and finished goods to include Retain, Coat Weight, Cure and any additional testing as required by the Product Requirement Sheet, (PRS) or Tech 11.
• Record and enter test results into the Scapa ERP System
• Perform all manufacturing audits prior to production and at required intervals.
• Maintain and organize product master files.
• Coordinate shop floor QC testing based on daily and weekly production schedule.
• Issue non-conformance report for any tested material that is out of specification.
• Perform visual inspections of materials being coated and slit/converted and immediately inform coating/converting operators of any defects.
• Interfaces with Quality Assurance and Production scheduling in the preparation and reviewing of slitting specifications.
• Evaluates product quality based on product specifications and makes appropriate usage decisions.
• Responsible for setting up test equipment.
• Maintaining inventory of QC lab MRO items
• Responsible for maintaining all related files and documents according to Good Documentation Practice, (GDP).
• Assists in training new QA Inspectors and manufacturing personnel.
• Participates as a team member in continuous improvement events.
• Maintain QC test equipment and calibration status.
• Assists quality engineers and quality technicians with gage R&R, and other validation activities.
• Follows safety rules and keeps the work area in a clean and orderly manner.
• Complies with company attendance policies.
• Issue Supplier Complaints in the ICS, (Internal Complaint System), for nonconforming raw material.

Qualifications

Required

• Minimum of 2 years' experience in Q. A. or Q. C. manufacturing environment.
• High School diploma required, bachelor's degree highly preferred.
• Familiar with basic measurements, test equipment and basic math skills.
• Medical device industry experience preferred.
• Ability to communicate and work within a team environment.

Preferred

• 2 years' experience in Quality Assurance or Quality Control.
• 2 years' experience in medical device or industrial manufacturing.
• Associate degree in chemistry, physical sciences, or tech field. Relevant job experience may be considered in place of a 2-year degree.
• Able to collaborate and work well with others.

WHAT WE OFFER

Mativ benefits say a lot about how we care for each other. Our employees and their families have many different needs. As a result, our benefits offer choices on many levels and are high in quality, competitive in the marketplace, and affordable.

ABOUT MATIV

Mativ Holdings, Inc. is a global leader in specialty materials headquartered in Alpharetta, Georgia. The company connects, protects, and purifies the world every day through a wide range of critical components and engineered solutions that solve our customers' most complex challenges. We manufacture on three continents and generate sales in nearly 100 countries through our family of business-to-business and consumer product brands. The company's two segments, Filtration & Advanced Materials and Sustainable & Adhesive Solutions, target premium applications across diversified and growing end-markets, from filtration to healthcare to sustainable packaging and more. Our broad portfolio of technologies combines polymers, fibers, and resins to optimize the performance of our customers' products across multiple stages of the value chain. Our leading positions are a testament to our best-in-class global manufacturing, supply chain, and materials science capabilities. We drive innovation and enhance performance, finding potential in the impossible.