PV Project Manager and Deputy QPPV – Mendrisio site (Ticino) — Sintetica SA
- Location
- Mendrisio
- Contract
- other
- Posted
- —
Role overview
PV Project Manager and Deputy QPPV – Mendrisio site (Ticino) — Sintetica SA, Mendrisio (TI).
We do so in close cooperation with clinical experts, who shape our understanding of their unmet needs and drive our efforts to address them.
With this trust and insight, we push the limits of science and technology to make therapies safer for patients and easier to perform.
- PV Project Manager and Deputy QPPV – Mendrisio site (Ticino) — Sintetica SA, Mendrisio (TI).
- We do so in close cooperation with clinical experts, who shape our understanding of their unmet needs and drive our efforts to address them.
- Key Responsibilities
- Lead and coordinate Pharmacovigilance projects, ensuring timely delivery and alignment with business and regulatory requirements.
- and skills
- Master’s degree or PhD in a scientific or healthcare discipline (e.g.
Main responsibilities
- Key Responsibilities
- Lead and coordinate Pharmacovigilance projects, ensuring timely delivery and alignment with business and regulatory requirements.
- Act as Deputy QPPV, ensuring continuity of Pharmacovigilance operations, regulatory compliance, and appropriate oversight during periods of QPPV absence.
- Oversee global Pharmacovigilance system activities, ensuring compliance with Swiss, EU, and international regulations.
- Support the maintenance of Swiss and Global Pharmacovigilance System Master File (PSMF), coordinating input from internal functions and external partners.
- Coordinate safety communications including Direct Healthcare Professional Communications (DHPCs).
- Oversee the preparation and submission of aggregate safety reports (PSUR/PBRER, DSUR).
- Ensure end-to-end oversight of adverse event collection, assessment and reporting from all sources (spontaneous reports, clinical trials, literature, partners).
- Maintain strong collaboration with the affiliate, commercial partners and external vendors to ensure global PV compliance.
- Oversee the Global Safety Database and support system maintenance, upgrades and configuration activities.
Key requirements
- and skills
- Master’s degree or PhD in a scientific or healthcare discipline (e.g.
- Pharmacy, Medicine, Biology, Chemistry or related field).
- At least 5–8 years of experience in Pharmacovigilance within a pharmaceutical company or CRO.
- Strong knowledge of EU GVP modules, ICH guidelines, Swiss and global PV regulations.
- Previous experience as Deputy QPPV or in a senior PV role is strongly preferred.
- Experience with signal management, aggregate reporting, PSMF, and safety databases (e.g.
- Veeva Vault Safety).
- Solid experience in PV project management and cross-functional coordination.
- Excellent command of written and spoken Italian and English;
- French is a plus.
- Familiarity with regulatory inspections and compliance processes is an advantage.
What the company offers
- PV Project Manager and Deputy QPPV – Mendrisio site (Ticino) Founded in 1921 and headquartered in Mendrisio (Switzerland), Sintetica's mission is to continuously strive to improve therapies by enhancing its products' formulations and usability for the benefit of clinicians and patients.
- Lead signal management activities and contribute to the benefit-risk evaluation of Company’s products.
Additional details
- Qualifications and skills
Questions about this listing
What salary does Sintetica SA offer for this role?
Sintetica SA lists CHF 68'000 - 103'000 gross per year for this position in Mendrisio. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Sintetica SA offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Sintetica SA during the application process, since these details can vary by role even within the same contract category.
Do I need the G permit to apply for this role in Ticino as an Italian cross-border worker?
Yes, if you are resident in Italy within the 20 km border zone. The Swiss employer files the G-permit application at the Ticino cantonal migration office after the contract is signed — first issuance takes 2-6 weeks, then automatic yearly renewal for as long as the employment continues. Weekly return to your Italian home is required to keep the status.
How do I apply for this position at Sintetica SA?
Use the "Apply now" button on this page — it links directly to Sintetica SA's original listing at app.ncoreplat.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
