Specialist I Quality Control
Core
Provide quality expertise and support for pMDI projects, laboratory design, and GMP compliance in a pharmaceutical manufacturing setting.
Role type
Specialist I Quality Control (Pharmaceutical Manufacturing)
Builds
pMDI projects, GMP-compliant facilities and equipment systems
Domain
Pharmaceutical manufacturing / Quality Control / GMP
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
laboratory operations, GMP compliance, quality documentation, process development, database management, cross-functional collaboration, regulatory adherence, technical capability maintenance
Preferred skills
continuous improvement, automation design, project milestone support
Technologies
GPQS, ECMS, GVLMS databases
Responsibilities
Provide quality support to achieve project milestones; Assist in developing laboratory quality control standards and processes; Prepare and maintain documents and reports related to laboratory design and quality control; Design automated digital processes to support QC operations; Support quality control work for GMP-related facilities and equipment systems; Complete daily experiments following job operating procedures and guidelines.
