Quality Assurance Pharmacovigilance Specialist

JR Italy; Varese; In loco; EUR 45.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company is seeking a Quality Assurance Pharmacovigilance Specialist in Varese. The role involves managing QA activities, ensuring compliance with industry standards, and supporting pharmacovigilance systems, ideal for candidates with a strong pharma background and fluency in English.

Competenze

• Previous experience in a similar role within pharmaceutical companies or PV CROs.
• Strong understanding of QA standards.
• Fluent in English, both written and spoken.
• Willingness to travel periodically.

Mansioni

• Manage QA activities to ensure compliance with GVP and regulations.
• Oversight and coordination of pharmacovigilance audits.
• Support in the review and update of the Pharmacovigilance System Master File.

Conoscenze

Quality Assurance standards

Good Pharmacovigilance Practices (GVP)

Risk assessment management

Descrizione del lavoro

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Quality Assurance Pharmacovigilance Specialist, varese

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Client:

Pharma Point

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

833256057945771212833712

Job Views:

2

Posted:

10.06.2025

Expiry Date:

25.07.2025

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Job Description:

For a leading pharmaceutical company, Pharma Point is looking for a

Quality Assurance Pharmacovigilance Specialist

The selected candidate will be responsible for ensuring the development, implementation, and maintenance of the company’s Quality Management System in the area of Pharmacovigilance, in accordance with the quality standards of the Group.

Key Responsibilities:

• Management of Quality Assurance activities to ensure compliance with Good Pharmacovigilance Practices (GVP) and applicable regulations
• Management of SOPs/Work Instructions related to pharmacovigilance processes
• Oversight and coordination of pharmacovigilance audits
• QA review/approval of deviations, CAPAs, and change controls related to PV topics
• Support in the review and update of the Pharmacovigilance System Master File
• Risk assessment management to prioritize audits (affiliates, partners, vendors, PV system)

Requirements:

• Previous experience in a similar role within pharmaceutical companies and/or PV CROs
• Strong understanding of Quality Assurance standards
• Willingness to travel periodically
• Fluent in English, both written and spoken