Join to apply for the Supplier Quality Engineer role at Katalyst CRO .

Please double check you have the right level of experience and qualifications by reading the full overview of this opportunity below. Responsibilities:

Manage the complete supplier quality lifecycle, including verification of IQ/OQ/PQ activities.

Review and approve supplier documentation and conduct supplier site visits as required.

Implement and oversee supplier quality processes in compliance with ISO 13485, 21 CFR 820, and related standards.

Conduct supplier-related risk management and generate weekly/monthly project progress dashboards.

Qualifications:

10+ years of proven experience, including 4+ years in medical devices domain and supplier management preferred.

Knowledge of supplier quality activities, ISO 13485, 21 CFR 820, and purchasing controls.

Hands-on experience with IQ/OQ/PQ activities.

Experience reviewing and approving supplier documentation and conducting supplier site visits.

Additional Information:

Seniority level: Mid-Senior level

Employment type: Contract

Job function: Quality Assurance

Industry: Pharmaceutical Manufacturing

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