Quality Control Technician, Pharmaceutical Manufacturing
Overview
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.
What You'll Do8
- 1Represent the Quality Unit during manufacturing operations, acting as the customer on site to verify cGMP compliance and enforce local, state, and federal regulations
- 2Perform scheduled walk-throughs of formulation, sample/pre-weigh, filling areas, and the Warehouse to monitor quality and identify risks
- 3Conduct AQL visual inspection of finished goods to ensure product quality meets specification
- 4Execute Environmental Monitoring of Class C production areas, collecting samples to verify cleanliness and contamination control
- 5Review line clearance and production area setup before each new batch or operation to prevent cross-contamination
- 6Provide quality approval and acceptance for raw materials, components, and finished products, including release decisions
- 7Review packaging, product labels, cleaning logs, and maintenance logs, and support quality investigations
- 8Collect retention samples and monitor drug storage conditions to maintain product stability
Requirements7
- 1High School Diploma or GED required; Associates degree in scientific discipline preferred
- 22+ years of pharmaceutical experience in a quality role, with hands-on cGMP and USP knowledge
- 3Certified Pharmacy Technician (CPhT) credential preferred
- 4Strong attention to detail and quality-driven mindset with a results orientation
- 5Proven organizational and time management skills to handle multiple tasks
- 6Aptitude for decision-making and performing risk assessments
- 7Good computer skills with basic knowledge of Microsoft programs
Salary Insight
Salary not disclosed in listing
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
Mark Cuban Cost Plus Drug Company
VerifiedCompliance Manager, Pharma cGMP & QMS
You own compliance for pharmaceutical operations at Mark Cuban Cost Plus Drug Company, a mission-driven organization expanding access to affordable medicines. You coordinate document control, investigations, and audit readiness across manufacturing, laboratory, and distribution. You work directly with quality assurance, regulatory, and operations teams to maintain FDA cGMP compliance. This role offers the chance to shape a high-impact compliance program from the ground up, with direct influence on patient safety.
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.
Catalent
VerifiedQuality Control Technician I at Catalent
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.
TriCom Quest
VerifiedQuality Control Technician, Food Manufacturing
You will own product quality for an international food manufacturer in Los Angeles, checking raw materials, intermediates, and finished goods to keep every batch within specification. You will join a QC team that works nights and weekends, reporting through a structured quality system. This role stands out for its direct impact on food safety and the chance to master ATP testing, microbiological testing, and aseptic techniques.
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.
Mission Critical Group
VerifiedQuality Control Technician, Manufacturing & Inspection
You own quality assurance for Mission Critical Group's manufacturing network, ensuring ISO9001 standards and customer specifications drive every inspection. You interpret drawings, run audits, and document nonconformances that keep critical power systems online. Work with production teams across S.T.E.M.-based disciplines in an onsite Philadelphia role. This position stands apart through direct influence on CAPA and 8D problem-solving for mission-critical infrastructure.