Supplier Quality Specialist

This job was posted by https://www.kansasworks.com : For more

information, please see: https://www.kansasworks.com/jobs/13625139

## Who We Are

Since 1990, weve grown into a global leader in personalized medicine.

Today, our 5,000 energetic employees are based in 80 locations in

Europe, North America, South America, Africa and Asia-Pacificand are

working together to support over 200,000 customers worldwide.

From compounding and natural products to software, equipment, and

genomics we deliver smart, ready-to-use solutions that make healthcare

better.

Were passionate, science-driven, and always looking for new ways to

improve lives. ??

Explore your future at[Fagron Career

Site](https://fagron.jobsmarket.site/pages/en-gb/jobs).

## About The Job

The Supplier Quality Specialist is responsible for ensuring that

suppliers consistently deliver materials, components, and services that

Meet Company Quality Standards, Regulatory Requirements, And Customer

expectations. This role works closely with suppliers, procurement,

manufacturing, engineering, and quality teams to drive continuous

improvement and resolve quality issues.

**Key Responsibilities**

• Evaluate and qualify new suppliers through audits, assessments, and
  
  

performance reviews.

• Monitor supplier quality performance using key metrics reported.
• Investigate supplier-related quality issues and lead root cause
  
  

analysis activities.

• Review and approve supplier corrective and preventive action plans
  
  

(CAPA) utilizing the Supplier Notification and SCAR programs.

• Collaborate with purchasing and engineering teams during supplier
  
  

selection and development processes.

• Analyze quality data and prepare reports on supplier performance
  
  

trends.

• Ensure compliance with applicable standards, regulations, and
  
  

customer requirements.

• Support new product introductions by validating supplier processes
  
  

and capabilities.

• Drive continuous improvement initiatives to reduce defects, improve
  
  

quality, and lower costs.

• Maintain supplier quality documentation, records, and audit reports.
• Participate in audits to ensure compliance with quality management
  
  

systems and industry standards (in collaboration with the North

American Teams).

## Basic Qualifications

• High School Diploma and preferred cGMP experience in a
  
  

pharmaceutical manufacturing company or equivalent combination of

Education And CGMP Experience In a Required.

• Experience with quality systems, aseptic technique, cGMP document
  
  

review, quality investigations, CAPA, Change Control and

MasterControl preferred.

• Proficient in MS Office programs, including Word and Excel.
• Ability to process information rapidly from multiple sources and
  
  

communication channels.

• Ability to handle a high volume of work and rapidly adapt to
  
  

changing environment.

## What\'s on Offer?

Fagron offers its associates competitive salaries and a wide range of

benefits including a 401(k) plan with a company matching contribution;

medical, vision and dental; health savings account (HSA); holiday/paid

time off.

At Fagron, youll find plenty of chances to grow both personally and

professionally. We work in an open, dynamic environment where your ideas

and talents can shine.

## Ready For The Challenge?

Were proud to be an equal opportunity employer. ?? Diversity makes us

stronger, and were committed to creating an inclusive workplace where

everyone feels welcome.\

\

Fagron US is committed to creating a diverse environment and is proud to

be an equal opportunity employer. All qualified applicants will receive

consideration for employment without regard to race; creed; color;

religion; national origin; sex; age; disability; sexual orientation;

gender identity or expression; genetic predisposition or carrier status;

veteran, marital, or citizenship status; or any other sta us protected

by law.