Supplier Quality Specialist page is loaded
Supplier Quality Specialist
Apply locations Kansas City, MO Philadelphia, PA
time type Full time posted on Posted 3 Days Ago
time left to apply End Date: May 28, 2025 (24 days left to apply)
job requisition id 0087919
Position SummaryCatalent, Inc. is a leading global contract development and manufacturing organization (CDMO) dedicated to developing, manufacturing, and supplying products that improve lives. We support pharma, biotech, and consumer health clients from product development to full lifecycle supply, with extensive experience and technology across 40+ sites worldwide.
Catalent’s Kansas City facility specializes in Oral & Specialty Drug Delivery, Biologics Analytical Services, and Clinical Supply Services, providing services from formulation to manufacturing. It is also a Center-of-Excellence for Biologics Analytical Services.
This role is based at our Kansas City site and involves ensuring compliance with standards by managing supplier quality programs, conducting audits, maintaining records, and supporting supplier assessments and compliance activities.
Position DetailsThis is a full-time, on-site salary position: Monday – Friday, 1st shift. Location options include Kansas City, Philadelphia, or San Diego.
Why Join Catalent?- Defined career paths and performance reviews
- Inclusive culture and positive environment
- Opportunities for growth and development
- Comprehensive benefits including health, wellness, and retirement plans
- Supportive of education and wellness initiatives
- Engaged in community and sustainability efforts
- Committed to quality and patient safety
The Role- Manage supplier lists and quality programs
- Conduct and report audits for domestic and international suppliers
- Maintain supplier approval documentation
- Support and execute quality agreements, audits, risk assessments, and change controls
- Evaluate impact of supplier changes and monitor license renewals
- Liaise with suppliers on compliance with regulatory updates
- Other duties as assigned
The Candidate- High School Diploma or GED with 6+ years in Quality/Pharma, or Bachelor’s with 2+ years
- Experience in supplier auditing and report writing; certification preferred
- Knowledge of GMP/GDP/GCP regulations, especially related to sourcing and distribution
- Project management skills and system experience (JDE, Trackwise) preferred
- Ability to travel domestically and internationally (~25%)
- Physical ability to perform job functions including lifting up to 40 pounds
Additional Information- Catalent promotes a diverse, inclusive, and patient-focused culture
- Equal Opportunity Employer and accommodations for disabilities
- No unsolicited agency resumes accepted
- Be aware of fraudulent requests for personal information
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About CatalentWe are committed to innovation, growth, and making a difference in patients’ lives. Join us to develop your career in a dynamic environment focused on meaningful work.