Senior TPM QA Lead – External Manufacturing

Abbott

Fatih

Presencial

TRY 350.000 - 550.000

Jornada completa

Hace 5 días

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Descripción de la vacante

Abbott in Istanbul is seeking a TPM QA Sr. Associate to oversee quality for third party manufacturers and ensure cGMP compliance. You will manage investigations, deviations, CAPAs and product release support, with cross‑functional collaboration across QA, Regulatory, Manufacturing and Supply Chain.

The role requires strong analytical skills, English proficiency, and up to 40% travel domestically and internationally. Location: Istanbul, Türkiye.

Formación

Bachelor’s degree in pharmacy, chemistry, chemical engineering, or related scientific discipline.
5–7 years of QA, QC, and/or pharmaceutical manufacturing experience in a GMP-regulated environment.
Good knowledge of cGxP, ICH guidelines, and applicable regulations for pharma products and materials.
Understanding of manufacturing processes, labs, quality systems, and validation activities.
Willingness to travel domestically and internationally up to 40%.

Responsabilidades

Ensure quality and compliance performance of assigned TPMs, adhering to cGMP and QTAs.
Lead investigations, deviations, CAPAs, PQRs, validations, and product release support.
Review TPM documentation: MBRs, packaging records, validation and stability reports.
Drive quality oversight via audits, supplier qualification, and cross‑functional projects.
Coordinate with Supply Chain, Regulatory, Operations, and other stakeholders.