Lead QP Quality Manager — GMP & Regulatory Compliance

Ecolab; Verona; In loco; EUR 60.000 - 89.000; Tempo pieno

Vantaggi offerti da questo lavoro

Annual bonus

Benefits package

Descrizione del lavoro

Ecolab is seeking a Quality Manager in Verona to ensure medicinal products are manufactured, tested, certified, and released in full GMP compliance. You will balance regulatory obligations with operational needs and lead audits and inspections with regulators.

Ideal candidates have 7–10 years in pharma, QA/QC/regulatory expertise, and would relocate to Verona to drive continuous quality improvements at the site.

Competenze

• Valid AIFA Qualified Person Eligibility Certificate.
• Degree in Pharmacy, Chemistry, Pharmaceutical Chemistry and Technology (CTF), or a related scientific discipline.
• Registration with the Order of Chemists or Pharmaceutical Chemists and Technologists (may be completed after joining the company).
• 7-10 years of experience within the pharmaceutical industry.
• Experience working in GMP-regulated manufacturing sites.
• Strong background in Quality Assurance, Quality Control, Regulatory Affairs, or Compliance.

Mansioni

• Perform batch certification and release in accordance with applicable pharmaceutical regulations.
• Ensure ongoing GMP compliance across manufacturing and quality operations.
• Review and manage deviations, non-conformances, CAPAs, and customer complaints.
• Support and participate in internal, external, and supplier audits.
• Collaborate closely with Quality Assurance, Quality Control, Manufacturing, and Site Leadership teams.
• Lead interactions with regulatory authorities during inspections, including AIFA and other health authorities.

Conoscenze

AIFA Qualified Person eligibility

QA/QC/Regulatory affairs

GMP manufacturing experience

API experience

Interpersonal skills

Formazione

Pharmacy/CTF degree (or related science)

Registration with Order of Chemists or Pharmaceutical Chemists and Technologists

Descrizione del lavoro

Ecolab is seeking a Quality Manager in Verona to ensure medicinal products are manufactured, tested, certified, and released in full GMP compliance. You will balance regulatory obligations with operational needs and lead audits and inspections with regulators.

Ideal candidates have 7–10 years in pharma, QA/QC/regulatory expertise, and would relocate to Verona to drive continuous quality improvements at the site.