Quality Control Technician I at Catalent
Overview
Join Catalent's Kansas City facility as a Quality Control Technician I to own sampling tasks and support analytical services. This full-time onsite role involves independent work within a dynamic pace and meaningful projects. You will contribute to GMP compliance and collaborate across teams while maintaining safety standards.
What You'll Do8
- 1Perform sampling of raw materials and finished products using calibrated equipment
- 2Prepare sampling packets and update inventory records
- 3Ship release samples according to established procedures
- 4Maintain GMP knowledge and document all activities
- 5Investigate deviations related to material sampling
- 6Attend training sessions and keep SOPs current
- 7Assist colleagues during team sampling events
- 8Support project timelines through timely completion of tasks
Requirements6
- 1High School Diploma or GED minimum requirement
- 2Two years pharmaceutical experience with inspection or sampling
- 3Ability to lift up to 50 pounds and operate pallet jack
- 4Strong math and scientific reasoning skills
- 5Experience with face masks and confined space respiratory protection
- 6Valid ID and work authorization for onsite position
Salary Insight
Salary not disclosed in listing
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
Catalent Company
VerifiedQuality Assurance Associate at Catalent
Join Catalent to lead quality initiatives at our Windsor site. You will drive compliance and continuous improvement while preventing quality issues. This role focuses on proactive oversight and team coaching.
Actalent
VerifiedQuality Control Laboratory Technician Actalent
Quality Control Laboratory Technician at Actalent in New York City leads quality and food safety initiatives ensuring compliance with SQF GMP Kosher and FDA standards. The technician collects tests evaluates samples approves blends performs QC activities maintains documentation coordinates third party labs and provides quality oversight during second shift operations. This newly created role offers hands on experience in production and laboratory settings while shaping food safety culture.
Colorcon
VerifiedQuality Control Manager, Pharmaceutical & cGMP
Own the Quality Control laboratory at Colorcon's West Point and Harleysville sites, leading a team of chemists and microbiologists to ensure safe, compliant, and reliable support of manufacturing operations. This role drives laboratory compliance, operational performance, and team development while aligning capabilities with business growth. Partner with cross-functional teams including Manufacturing, Quality Assurance, and Regulatory to reduce risk and improve quality performance. The position reports to the Senior Quality and Regulatory Manager, offering a visible leadership opportunity in a global pharmaceutical supplier. This role stands out for its focus on continuous improvement and building a culture of accountability and technical excellence.
Creative Testing Solutions
VerifiedQuality Specialist I, cGMP Lab Testing
You own final approval and release of cGMP test results for biological samples at Creative Testing Solutions. You apply quality methodologies to ensure every batch meets FDA and CLIA standards before it reaches lab customers. You work with a team of quality specialists and lab personnel in Charlotte, NC. This role offers direct impact on patient safety and a clear path to Quality Specialist II and III.
SkySource Solutions
VerifiedQuality Assurance Technician 2nd Shift
Quality Assurance Technician 2nd Shift Phoenix Arizona onsite payroll
Mark Cuban Cost Plus Drug Company
VerifiedQuality Control Technician, Pharmaceutical Manufacturing
Join the Quality Unit at Mark Cuban Cost Plus Drug Company as a Quality Control Technician, owning quality oversight for pharmaceutical manufacturing operations in Dallas. You represent the Quality Unit during production, verifying compliance with cGMP and USP guidelines across formulation, filling, and warehouse areas. Working alongside manufacturing and quality teams, you perform audits, in-process testing, and environmental monitoring to secure product integrity. This onsite role stands out by pairing hands-on production floor presence with quality release decisions for raw materials and finished goods.