QC Inspector - Third Shift

MATIV HOLDINGSWindsor, CT
121d

About The Position

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.

Requirements

  • 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.

Nice To Haves

  • 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.

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.

Benefits

  • Medical, dental and vision insurance.
  • Consumer-Driven Health Plan (CDHP).
  • Preferred Provider Organization (PPO).
  • Exclusive Provider Organization (EPO).
  • Company-paid basic life insurance and Additional voluntary life coverage.
  • Paid vacation and competitive personal time off.
  • 401(k) savings plan with company match.
  • Employee assistance programs - available 24/7 to you and your family.
  • Wellness and Work Life Support - career development and educational assistance.

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Industry

Chemical Manufacturing

Education Level

High school or GED

Number of Employees

5,001-10,000 employees

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