GMP Biologics QC Technician | Lab Operations Lead

Leanbio SL

Sant Quirze del Vallès

Presencial

EUR 32.000 - 46.000

Jornada completa

hace 12 horas
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Descripción de la vacante

Leanbio SL in Sant Quirze del Vallès is seeking a Quality Control Technician to join the brand new Barcelona-area GMP facility. You will execute and supervise protein analysis, ensure ALCOA+ data integrity, maintain documentation, and support QC lab operations.

The role requires advanced training in protein analysis and 3+ years of QC experience in a GMP pharmaceutical environment. You will collaborate with QA, Production and MSAT to uphold quality and compliance.

Formación

  • Advanced training in protein analysis with 3+ years of QC in GMP pharma.
  • Hands-on experience with physicochemical, biochemical, and microbiological methods.
  • Strong ALCOA+ data integrity and GMP documentation knowledge.
  • Experience with OOS/Deviations, CAPAs, and change control.
  • Familiarity with laboratory equipment calibration and QC workflows.

Responsabilidades

  • Execute and supervise protein analysis to evaluate quality attributes.
  • Maintain accurate documentation in lab notebooks or LIMS.
  • Manage QC Lab processes and inventory of reagents.
  • Investigate OOS/OOT and report deviations, implement CAPA.
  • Calibrate and qualify equipment; ensure safety and cleanliness.
  • Collaborate with QA, Production, and MSAT as needed.

Conocimientos

Protein analysis
GMP compliance
ALCOA+ data integrity
Documentation in LIMS
QC Lab management
Assay supervision
Analytical methods
OOS/Deviations handling

Educación

Advanced protein analysis training

Herramientas

LIMS

Descripción del empleo

Leanbio SL in Sant Quirze del Vallès is seeking a Quality Control Technician to join the brand new Barcelona-area GMP facility. You will execute and supervise protein analysis, ensure ALCOA+ data integrity, maintain documentation, and support QC lab operations.

The role requires advanced training in protein analysis and 3+ years of QC experience in a GMP pharmaceutical environment. You will collaborate with QA, Production and MSAT to uphold quality and compliance.

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