Quality Assurance Pharmacist — GMP & Compliance Leader

Excelya; Boulogne-Billancourt; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

Excelya is seeking a Quality Assurance Pharmacist to strengthen our Quality team in France and support pharmaceutical quality systems, product quality activities, and regulatory compliance initiatives.

You will manage the QMS, coordinate documentation, participate in audits and inspections, and drive continuous improvement across manufacturing and quality functions. Fluent English is required; PharmD and QA experience in pharma are essential.

Formación

• PharmD mandatory and strong QA experience in pharmaceutical industry.
• Experience in pharmaceutical manufacturing or production environments is desirable.
• PRI registration is an asset.

Responsabilidades

• Maintain the Quality Management System (QMS) including SOPs and records.
• Coordinate document lifecycle activities: creation, review, approval, archiving, periodic reviews.
• Deliver GxP and quality training programs.
• Participate in internal audits, supplier audits, and health authority inspections.
• Manage deviations, CAPAs, change controls, RCA, and risk management activities.
• Review and approve batch release documentation and distribution-related quality activities.
• Collaborate with Manufacturing, Supply Chain, Regulatory Affairs, Pharmacovigilance, and Quality stakeholders.
• Monitor quality KPIs and contribute to management reviews.

Conocimientos

GxP Quality

Quality Assurance

Regulatory compliance

Audits

Risk management

CAPA management

Deviation handling

Cross-functional collaboration

Process improvement

English fluent

Educación

Doctor of Pharmacy (PharmD)

PRI registration (asset)

Herramientas

TrackWise

EDMS

SAP

Descripción del empleo

Excelya is seeking a Quality Assurance Pharmacist to strengthen our Quality team in France and support pharmaceutical quality systems, product quality activities, and regulatory compliance initiatives.

You will manage the QMS, coordinate documentation, participate in audits and inspections, and drive continuous improvement across manufacturing and quality functions. Fluent English is required; PharmD and QA experience in pharma are essential.