Senior QMS & GMP Compliance Specialist

Chiesi; Napoli; Ibrido; EUR 65.000 - 95.000; Tempo pieno

Vantaggi offerti da questo lavoro

Comprehensive healthcare programs

Work-life balance initiatives

Relocation support

Flexible working arrangements

Remote work options

Descrizione del lavoro

Chiesi in Napoli, Campania, Italy, seeks a Quality & Compliance System Senior Specialist to lead and optimize the QMS across the site, ensuring GMP, FDA and EU compliance and reporting on performance.

You will collaborate with production, engineering and procurement and other functions to drive quality improvements, manage inspections, CAPAs, training, and documentation, shaping robust processes for materials, manufacturing and release specifications.

Competenze

• Degree in scientific subjects (Chemistry, Pharmaceutical Chemistry and Technology, Engineering).
• At least 5 years of pharmaceutical/biopharmaceutical QA/Production/Process Technology experience.
• Excellent knowledge of EU and FDA pharmaceutical guidelines.
• Fluent English (written and spoken).

Mansioni

• Develop and implement QMS processes, procedures, and documentation to meet quality standards.
• Monitor and analyze quality data, identify trends, and drive improvement actions.
• Prepare periodic QMS performance reports for management.
• Collaborate with production, engineering, procurement and other functions to resolve quality issues.
• Investigate quality problems, identify root causes, and implement corrective and preventive actions (CAPA).
• Govern and promote a culture of quality and continuous improvement across the site.
• Share best practices and ensure activities comply with company procedures.

Conoscenze

QA experience

QMS knowledge

CAPA expertise

EU/FDA guidelines

English fluency

Formazione

Degree in Chemistry/Pharmaceutical Science/Engineering

Descrizione del lavoro

Chiesi in Napoli, Campania, Italy, seeks a Quality & Compliance System Senior Specialist to lead and optimize the QMS across the site, ensuring GMP, FDA and EU compliance and reporting on performance.

You will collaborate with production, engineering and procurement and other functions to drive quality improvements, manage inspections, CAPAs, training, and documentation, shaping robust processes for materials, manufacturing and release specifications.