QC VP

Emploi Taïwan

Titre du poste : QC VP

Entreprise : Adecco

Description du poste :

Lead and oversee the Quality Control (QC) function across all manufacturing sites, ensuring strict compliance with GMP, ICH, US FDA, EMA, and PIC/S standards.
Develop, implement, and maintain QC policies, SOPs, quality metrics, and laboratory systems to ensure data integrity and regulatory compliance.
Manage and supervise QC operations, including raw materials, in-process, and finished goods testing and batch release.
Collaborate closely with Quality Assurance (QA), Regulatory Affairs, Production, and R&D teams to ensure overall product quality.
Take leadership in internal and external audits, including inspections by health authorities such as TFDA, US FDA, and EU regulators.
Oversee deviation investigations, OOS/OOT management, CAPA execution, and change control processes.
Build and mentor a strong, high-performing QC team to support the company’s global manufacturing expansion and compliance goals.

Master’s or PhD degree in Pharmacy, Chemistry, Analytical Science, or related disciplines.
Minimum 15 years of experience in pharmaceutical quality control, with at least 5 years in senior leadership or VP-level roles.
Proven track record in managing QC operations in API or CDMO manufacturing environments.
Deep knowledge of global GMP regulations (FDA, EMA, WHO, PIC/S) and ICH Q-series guidelines.
Hands-on experience with regulatory inspections, compliance audits, and remediation plans.
Fluent in English (verbal and written); additional language skills are a plus.
Familiarity with LIMS, data integrity principles (ALCOA+), and electronic documentation systems.

Salaire attendu :

Localisation : Lujhu, Taoyuan City

Date du poste : Thu, 15 May 2025 07:32:19 GMT

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