Quality Inspector 3rd Shift (Monday - Friday 11:00PM - 7:30AM)

Working at Freudenberg: "We will wow your world!" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 52,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments.

At Freudenberg Medical, we make products that save and improve the lives of people every day, all around the world. We are a global provider for medical device design and manufacturing with more than 2,500 employees. Innovation is at the core of our company, and we are proud of our industry-leading quality, lean manufacturing, and focus on innovation in products and processing technologies. Freudenberg Medical is an exciting place to work with lots of opportunity to learn, develop, and grow your career. Come join us and together we can make a difference in the future of healthcare.

Some of your Benefits

401K Match: Save for retirement with the company's help.

Safe Environment: We strive to ensure safety remains a top priority, and provide a stable environment for our employees.

Sustainability & Social Commitment: We support social and sustainable projects and encourage employee involvement.

Diversity & Inclusion: We focus on providing an inclusive environment and recognize our diversity contributes to our success.

Corporate Events: We celebrate success as a team, because only together can we achieve our goals.

Beverly, MA

On-Site

Freudenberg Medical LLC

payments $23 - $26 per hour

You support our team as

Quality Inspector 3rd Shift (Monday - Friday 11:00PM - 7:30AM)

Responsibilities

• Measure and record product quality using, visual, mechanical and optical gauging instruments.
• Inspect incoming raw material to insure that all quality requirements have been met per acceptance activities and material specifications.
• Ensure conformance to certifications for all materials and components received.
• Identify and segregate non-conforming material for material review board (MRB) disposition
• Generate NCMR’s and assign owners.
• Participate in Gauge R&R’s
• Perform applicable materials testing per acceptance activities and/or specification.
• Strong knowledge of interpreting drawings, customer specification, test methods, and inspection criteria.
• Maintain complete, legible, and accurate records.
• Independently handle problems that arise within area of responsibility.
• Knowledge of cGMP’s.
• Knowledge of scheduling methods and ability to change priorities when directed by Supervisor/Manager.
• Interact effectively with other employees within the department and the company.
• Release product to next location upon completion within SAP system.
  
  

Qualifications

• High School/Trade School Diploma or GED
• Must have 2 years of experience in Quality Control
• Experience in the medical device industry preferred
  
  

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.