Referso Jobs

PV Analyst

Mundipharma · Posted Nov 10, 2026

Open

Tokyo, Tokyo, Japan
On-site
Full-time · Associate
3+ years

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PV Analyst

Mundipharma · Posted Nov 10, 2026

Open

Tokyo, Tokyo, Japan
On-site
Full-time · Associate
3+ years

Apply with Referso

Auditeur GVP (H/F)

SERVIER MONDE · Posted Oct 29, 2026

Open

Gif-sur-Yvette, Île-de-France, France
3+ years

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Responsable de la planification, conduite et suivi des audits GVP pour garantir la conformité réglementaire et qualité interne.

Responsibilities

Préparer, réaliser et rapporter les audits GVP conformément au plan qualité annuel.
Accompagner les équipes auditées dans la mise en œuvre des actions correctives et préventives (CAPA).
Assurer le suivi des audits jusqu’à leur clôture et analyser les indicateurs de performance.
Gérer l’externalisation de certaines activités d’audit (sélection, pilotage, validation).
Participer à la préparation et au suivi des inspections GVP.

Requirements

Pharmacien
Médecin
Master scientifique avec formation en assurance qualité

Skills

GVP standards internationaux audits GVP CAPA inspections GVP

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Manager, Drug Safety Operations

Precigen, Inc · Posted Nov 10, 2026

Open

Germantown, Maryland, United States
Manager
3–5 years

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Lead day‑to‑day pharmacovigilance operations, managing vendor relationships, ensuring regulatory compliance, and supporting safety reporting.

Responsibilities

Manage day‑to‑day relationships with PV vendors
Coordinate vendor selection activities
Support negotiation and maintenance of contracts, SOWs, change orders, and PVAs/SDEAs
Track and report KPIs and SLAs
Monitor vendor adherence to US and international PV regulations

Requirements

Bachelor’s degree in life sciences, nursing, pharmacy, or a related field

Skills

pharmacovigilance vendor oversight safety databases Argus ICSR processing PV regulations GVP 21 CFR 312/314 ICH E2 series

Program Director, Strategy & Operations

Precigen, Inc · Posted Nov 10, 2026

Open

Germantown, Maryland, United States
Full-time · Director
10+ years

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The Head of Development's partner in running the business of the Development organization: Clinical Sciences & Operations, Clinical Development, Medical Affairs, Pharmacovigilance and Translational Sciences. The role owns planning, operating rhythm, budget and resource tracking, cross-functional initiatives and executive reporting for Development.

Responsibilities

Run the Development annual goals, operating plan and long-range planning cycle with the Head of Development and functional heads.
Translate corporate and pipeline priorities into functional plans, resourcing and budgets; track delivery against goals.
Prepare executive, leadership-team and board materials on the Development portfolio, progress and risks.
Run the Development leadership cadence: leadership team meetings, portfolio and program reviews, decision and action logs.
Coordinate cross-functional governance and interfaces across Clinical Development, Clinical Sciences & Operations, Medical Affairs, Pharmacovigilance and Translational Sciences.

Requirements

Bachelor's degree required
MBA
PMP
advanced scientific degree
Nice to have: small-biotech experience

Skills

clinical operations development program management R&D business operations

Senior Safety Technology Analyst

Parexel · Posted Nov 6, 2026

Open

Remote, India
Remote
Full-time · Senior
5+ years

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Drive the strategic implementation and operational excellence of Parexel's pharmacovigilance safety technology systems, ensuring regulatory compliance, system optimization, and delivery of advanced safety solutions.

Responsibilities

Lead the setup, configuration, and support of Parexel's safety database and associated systems, including new study implementations, periodic and ad-hoc report generation, expedited report rule configuration, and comprehensive end-user support
Direct the planning and execution of safety database handovers from clients to Parexel and from Parexel to clients at project completion
Design and deliver complex integration solutions between Parexel safety technologies and other applications to enhance operational capabilities
Represent Safety Technology Management in cross-functional collaboration with IT, Quality Assurance, and external auditors
Lead change management initiatives aligned with Software Development Life Cycle principles, including impact assessments, testing methodologies, system validation, and software updates

Requirements

BA/BSc in Engineering
BA/BSc in Computer Science
Nice to have: master's degree
Nice to have: mentorship
Nice to have: peer oversight

Skills

pharmacovigilance safety technology systems

Associate Director, Quality GCP

Verastem · Posted Nov 6, 2026

Open

Boston, Massachusetts, United States
Senior
7+ years

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Lead and manage GCP quality assurance activities across clinical programs, including audits, inspection readiness, and risk management.

Responsibilities

Develop and implement Quality Programs
Develop and implement risk-based GCP strategies
Manage and support development of GCP quality standards and controlled documents
Promote compliance and quality throughout the company
Build and maintain relationships with internal and external partners

Requirements

Bachelor’s degree in related Life Sciences discipline
Nice to have: advanced degree

Skills

GCP FDA regulations ICH guidelines GLP GVP clinical site audits clinical vendor audits Veeva systems

Safety & PV Specialist- Future Roles

Syneos Health · Posted Nov 6, 2026

Open

Gurugram, Haryana, India
Entry

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This is a talent pipeline posting for a Safety & PV Specialist role in India, focusing on ICSR processing, data entry, and regulatory reporting within biopharmaceutical solutions.

Responsibilities

Enter information into PVG quality and tracking systems for receipt and tracking ICSR
Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans
Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability
Enters data into safety database
Codes events, medical history, concomitant medications, and tests

Requirements

Bachelor’s Degree in life science
Registered Nurse
Pharmacist

Skills

Safety Database systems Medical terminology Clinical trial process (Phases II-IV)ICH GCP GVP Microsoft Office Suite Visio

Pharmacien Responsible

Valneva · Posted Nov 5, 2026

Open

Lyon, Auvergne-Rhône-Alpes, France
Hybrid
Full-time · Director
10+ years

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The Pharmacien Responsable is responsible for overseeing local pharmaceutical quality strategy, compliance, distribution, pharmacovigilance, and regulatory governance within France.

Compensation

Performance Bonus (on top of base salary)

Responsibilities

Define and oversee the local pharmaceutical quality strategy and ensure the effective implementation and continuous improvement of the Quality Management System (QMS).
Ensure pharmaceutical governance, quality oversight, inspection readiness and compliance across local and outsourced activities.
Oversee deviations, CAPAs, change controls, quality complaints, supplier qualification, audits and quality risk management.
Ensure pharmaceutical compliance across the French distribution network, including 3PLs, warehousing, transportation and cold-chain management.
Oversee product quality, batch traceability, recalls, withdrawals, temperature excursions and distribution-related quality incidents.

Requirements

Pharmacist qualified and registered with the French Order of Pharmacists (Section B)

Skills

GxP GDP GVP

PV Analyst

PV Analyst

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Auditeur GVP (H/F)

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Manager, Drug Safety Operations

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Program Director, Strategy & Operations

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Senior Safety Technology Analyst

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Associate Director, Quality GCP

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Safety & PV Specialist- Future Roles

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Pharmacien Responsible

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