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.

DESCRIPTION:

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 6pm-6am.

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.
Fluency in English both verbal and written
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.
Position Demands

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.