TPM QA Manager
Core
Managing quality oversight, compliance, and continuous improvement for external pharmaceutical manufacturing partners across the EMEA region.
Role type
Senior IC QA Manager (Third Party Manufacturing)
Builds
Ensures compliant manufacturing of pharmaceutical products by external partners
Domain
Pharmaceutical manufacturing / Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
cGMP regulations knowledge, pharmaceutical quality systems, stakeholder management, quality risk assessment, CAPA management, change control, audit support, technology transfer oversight
Preferred skills
Leadership experience, experience with sterile/liquid/solid dosage forms or APIs
Technologies
GMP, CAPA, Change Control, Quality Risk Assessment
Responsibilities
Leading quality oversight of external manufacturing partners, driving continuous quality improvement initiatives, managing quality performance monitoring and supplier compliance, leading investigations and quality risk assessments, supporting GMP audits and regulatory inspections, reviewing Quality Technical Agreements, acting as QA Lead during technology transfers and NPI
Seniority
Senior, hands-on IC