Senior R&D Quality Lead - GCP & Supplier Oversight

Takeda Pharmaceutical Co.

Warszawa

In loco

PLN 328.000 - 451.000

Tempo pieno

14 giorni+

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Descrizione del lavoro

Takeda Pharmaceutical Co. is seeking a senior CSSQ quality professional to oversee supplier and clinical audits across global partners. You will ensure GCP/GCLP/GVP compliance, drive CAPA management, and report risk metrics to senior leadership.

Applicants should have extensive experience in quality assurance within the pharmaceutical industry, strong cross-functional collaboration, and a track record of leading complex audit programs in a global environment.

Competenze

BSc in a scientific or allied health/medical field (or equivalent).
Minimum of 10 years of increasing responsibility in the global pharmaceutical industry, with at least 5 years in GCP/GCLP/GVP Quality/Compliance.
Champion a culture of quality and compliance across the organization.
Fluency in written and spoken English; additional languages a plus.

Mansioni

Executes strategic quality oversight activities across supplier audits and CSSQ programs.
Develops strategic audit plan with risk factors and audit frequency.
Maintains reporting of audit metrics and KPIs for proactive oversight.
Escalates significant compliance risks to senior management.
Leads CAPA management and audit closure for supplier audits.
Collaborates with global functions to support consultant auditor framework.