Deputy Local Qualified Person for Pharmacovigilance

Apsida Life Science; À distance; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading biotechnology firm in Nice is seeking a Deputy Local Qualified Person for Pharmacovigilance. This remote-based role involves ensuring compliance with EU pharmacovigilance legislation and supporting the Local QPPV in various regulatory activities. The ideal candidate will have a degree in a relevant scientific field and 2–4 years of pharmacovigilance experience, specifically with French regulations. Join a dynamic team and contribute to lifesaving protein therapeutics.

Qualifications

• Degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related scientific field.
• Minimum 2–4 years of pharmacovigilance experience, preferably including EU PV requirements.
• Experience working with French pharmacovigilance processes and local affiliates or distributors.
• Exposure to audits or inspections is an advantage.

Responsabilités

• Support to Local QPPV & Regulatory Compliance.
• Act on behalf of the Local QPPV during absences.
• Support interactions with the French competent authority.
• Escalate safety concerns promptly to the Local QPPV.
• Support oversight of PV vendors operating in France.

Description du poste

Deputy Local Qualified Person for Pharmacovigilance Apsida Life Science•Nice, FR

Job Title: Deputy Local QPPV

Location: France - remote-based

Duration: 12 months contract

Company Overview:

Apsida Life Science is currently partnering with a preclinical biotechnology company which focuses on innovative protein therapeutics derived from a naturally occurring human anti-inflammatory protein. Its proprietary protein fragment retains key therapeutic functions while offering enhanced stability and manufacturability.

Responsibilities:

• Support to Local QPPV & Regulatory Compliance
• Support the Local QPPV in maintaining compliance with EU pharmacovigilance legislation and French PV regulations.
• Act on behalf of the Local QPPV during planned or unplanned absences, ensuring uninterrupted PV coverage.
• Support interactions with the French competent authority (ANSM), including responses to regulatory requests, inspections, and audits.
• Escalate safety concerns, compliance issues, and significant deviations promptly to the Local QPPV and EU QPPV.
• Support oversight of PV vendors, partners, and distributors operating in France.
• Safety Case Management & Reporting

Qualifications:

• Degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related scientific field
• Minimum 2–4 years of pharmacovigilance experience, preferably including EU PV requirements
• Experience working with French pharmacovigilance processes and local affiliates or distributors
• Exposure to audits or inspections is an advantage

If you are interested in learning more, please reach out to Sweetness Zono at Apsida Life Science:

[e-mail]

[phone]

www.apsida.co.uk