Senior QA & Pharmacovigilance Leader — Remote/Hybrid

Veristat; Basel; Remote; CHF 180,000 - 240,000; Full time

Benefits offered by this job

Remote working (60-80%)

Flexible time off

Paid holidays

Health insurance (KTG)

Tuition reimbursement

Pension plans

Job summary

Veristat seeks an experienced Senior Quality Assurance and Pharmacovigilance Manager to lead QA and PV activities under Swiss and EU legislation. The role includes acting as QA Designee for SFL-DE and ensuring the integrity of the QMS across manufacturing and distribution of medicinal products.

The candidate should have 5–10 years of GxP experience, degree in life sciences or pharmacy, and strong knowledge of GMP and GDP, with English proficiency and local language capabilities.

Qualifications

• 5-10 years’ GxP experience and be trustworthy, including experience as RP (FvP) or DRP (stellv. FvP)
• Degree in pharmacy or in life sciences showing experience in manufacturing and/or distribution of ready-to-use medicinal products
• Knowledge of medicinal products and guidance, especially GMP and GDP
• Knowledge of GVP and GCP is advantageous
• Excellent written and spoken English; ability to interact with local authorities in German or French is beneficial

Responsibilities

• Act as Senior QA & PV Manager and maintain Swiss QMS per Swiss/EU legislation
• Support QA team to establish new or maintain existing Pharmaceutical QMS
• Act as QA Designee for SFL Pharmaceuticals Deutschland GmbH (SFL-DE) reporting to SFL-DE Head QA
• Collaborate with regulatory and cross-functional teams to ensure compliance and inspection readiness
• Contribute to continuous improvement for QA and PV processes

Skills

GxP

RP/DRP experience

GMP/GDP/GVP/GCP knowledge

English proficiency

Management experience

Education

Degree in Pharmacy or Life Sciences

Job description

Veristat seeks an experienced Senior Quality Assurance and Pharmacovigilance Manager to lead QA and PV activities under Swiss and EU legislation. The role includes acting as QA Designee for SFL-DE and ensuring the integrity of the QMS across manufacturing and distribution of medicinal products.

The candidate should have 5–10 years of GxP experience, degree in life sciences or pharmacy, and strong knowledge of GMP and GDP, with English proficiency and local language capabilities.