• Responsible for implementation, maintenance and improvement of the quality management systems.• Responsible for Management Review.• Maintenance of nonconformities and CAPAs.• Performance of supplier assessments.• Responsible for audits.

- Planning of analytical resources to ensure release of quality results according to deadlines- Support quality investigations and Corrective Action/Preventative Action (CAPA) plans for work falling under the Quality Control department.- Continuous Improvements and Change Controls- Auditing experience- Support of digitalization activities- Technical writing

- Part of the team starting up the QC laboratory within the new AZ Biomanufacturing Center and bringing the QC laboratory to GMP standards- Analytical Tech Transfers- Training of new employees- Subject Matter Expert (SME) within Bioassay- Interim Team Lead Bioassay (4 months)

• Project coordinator• Review and approval of bioassay results• Method development and qualification• Bioassay statistics and data trending• Client communication

• Plan, perform and report Potency assays for clients• Development and tech transfer of Potency assays• Data analysis using PLA software for bioassay analysis • Maintenance and qualification of equipment• Generation of Standard Operating Procedures and Methods• Culturing mammalian cells

Thesis: “Formation of the inhibitory KIR repertoire in human natural killer cells”