Quality Assurance Pharmacovigilance Specialist

JR Italy; Como; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company, Pharma Point, seeks a Quality Assurance Pharmacovigilance Specialist in Como, Italy. Responsibilities include ensuring compliance with Good Pharmacovigilance Practices and overseeing Quality Assurance activities. Ideal candidates will have relevant experience and a strong grasp of quality assurance standards.

Competenze

• Previous experience in a similar role within pharmaceutical companies and/or PV CROs.
• Strong understanding of Quality Assurance standards.
• Willingness to travel periodically.

Mansioni

• Management of Quality Assurance activities to ensure compliance with GVP and regulations.
• Oversight and coordination of pharmacovigilance audits.
• QA review of deviations, CAPAs, and change controls related to PV topics.

Conoscenze

Quality Assurance Standards

Pharmacovigilance Practices

Risk Assessment Management

Audit Coordination

Fluent in English

Descrizione del lavoro

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Quality Assurance Pharmacovigilance Specialist, como

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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:

331801157646784921633712

Job Views:

1

Posted:

11.06.2025

Expiry Date:

26.07.2025

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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