Wknd QC Inspector- Day Shift

Mativ Holdings, Inc.; Alpharetta (GA); Hybrid; USD 42,000 - 54,000; Full time

Benefits offered by this job

Shift differential

Training program

Job summary

Mativ Holdings, Inc. seeks a QC Inspector to ensure product quality from in-process to finished goods at its Alpharetta, GA site. You will conduct inspections, record results, and support the manufacturing team to meet specifications under supervision of Quality Engineering.

The role includes a 10% shift differential and on-site work with training conducted Monday–Thursday. Prior medical device industry experience is preferred, with opportunities to participate in continuous improvement

Qualifications

• Minimum 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

• Audits and tests in-process and finished goods per PRS/Tech 11.
• Record test results in ERP system.
• Coordinate QC testing with daily/weekly production schedules.
• Issue non-conformance reports for out-of-spec materials.
• Maintain QC lab files and calibration status.
• Assist in training new QA inspectors and manufacturing staff.

Skills

QA/QC experience

Team communication

Basic measurement

Math skills

Test equipment

Education

High School diploma

Bachelor's degree preferred

Tools

Test equipment

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.

**10% Shift differential included**

Training will be completed Monday - Thursday.

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 theICS, (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.