Krzysztof Tajchert

Coordination of NC and CAPA processes and site/product reviews preparation; Product transfer QA responsible person (3 combination drug eluting products); Implementation and improvement of QMS (e.g. project of implementation divisional OPs); Collaboration with other departments and suppliers in quality matters; Driving change management in quality area; Introduction of the best practices (e.g. Kaizen Blitz, Poka Yoke).

Supervision of production quality in OEM; Analysis of complaints and conducting CAPA processes; Processes verification and validation of testing methods; Supplier risk analysis; Report directly to senior stakeholders.

Leading and participation in Lean Six Sigma quality improvement programs; Conducting internal audits; Co-operation with suppliers in quality matters (complaints); Preparation of plans for control of raw materials; Creation and translation of engineering documents and leading appropriate trainings; Control over documentation and company QMS and trainings databases.

Organic Chemistry, Computational Chemistry