QC Inspector

Scapa Tapes North America; Windsor (CT); On-site; USD 40,000 - 75,000; Full time

Job summary

An established industry player is seeking a dedicated QC Inspector to join their dynamic team. This role involves performing critical inspections and tests throughout the manufacturing process to ensure compliance with specifications. The ideal candidate will bring at least two years of experience in quality assurance or control, preferably within the medical device sector. You will play a vital role in maintaining product quality and safety, collaborating closely with various teams to enhance operational efficiency. If you thrive in a fast-paced manufacturing environment and are passionate about quality, this opportunity is perfect for you.

Benefits

Medical, dental and vision insurance

401(k) savings plan with company match

Paid vacation and competitive personal time off

Employee assistance programs

Wellness and Work Life Support

Qualifications

• Minimum 2 years' experience in QA or QC manufacturing environment.
• Familiar with basic measurements and test equipment.
• Medical device industry experience preferred.

Responsibilities

• Perform inspections and tests throughout the manufacturing process.
• Record and enter test results into the Scapa ERP System.
• Issue non-conformance reports for any tested material out of specification.

Skills

Quality Assurance

Quality Control

Basic Math Skills

Team Collaboration

Education

High School Diploma

Bachelor's Degree

Associate Degree in Chemistry or Physical Sciences

Tools

Scapa ERP System

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.

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 6am-6pm.

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.

Position Demands

Conditions are that of a manufacturing environment:

• Air Temperatures can range from cold to hot.
• The atmosphere may contain dust, fumes, and odors.
• May include mechanical, electrical, chemical, explosive and radiation hazards.

Employees are required to wear Personal Protective Equipment (PPE) including:

• Safety shoes (steel toe or composite toe)
• Safety Glasses
• Bump Caps
• Protective Gloves, when performing certain tasks
• Hearing Protection, when required.
• Other personal protective equipment as required for certain tasks.

While performing the duties of this job the employee must meet the physical demands:

• Be able to lift a minimum of 50 pounds.
• Be able to work 12-hour shifts.
• Perform repetitive tasks.
• Routinely stand, sit, hear, walk, and talk.
• Reach, climb, bend, kneel, crouch, twist, and balance, sometimes in awkward or tight spaces.
• Have good close vision, depth perception, and the ability to focus.

WHAT WE OFFER

At Mativ, our benefits reflect how much we value and care for each other. We know that employees and their families have unique needs, so our comprehensive benefits offer flexibility, quality, and affordability. Here are just a few of the ways we support your well-being and that of your loved ones:

• 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

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.

Mativ and its subsidiaries are Equal Opportunity Employers. Qualified applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.