Gvp Consultant (Pv Auditor)

JR Spain; Madrid; A distancia; EUR 45.000 - 80.000; Jornada completa

Descripción de la vacante

An established industry player in regulatory compliance is seeking a skilled professional to lead Pharmacovigilance audits. This role involves planning, executing, and reporting audits while ensuring adherence to quality standards and regulatory requirements. The ideal candidate will possess expert knowledge of Pharmacovigilance legislation and a strong ability to manage projects effectively. Join a supportive and diverse organization that values collaboration and career development, offering an exciting opportunity to contribute to the pharmaceutical sector's highest standards.

Servicios

Training and Career Development

Supportive Work Environment

Global Collaboration Opportunities

Formación

• Expertise in conducting and leading Pharmacovigilance audits.
• Strong knowledge of national and international legislation.

Responsabilidades

• Plan and conduct Pharmacovigilance audits according to quality standards.
• Execute audits based on regulatory requirements and GVP.

Conocimientos

Pharmacovigilance Audits

Regulatory Requirements

Project Management

Problem Solving

Educación

Bachelor's Degree in Life Sciences

Descripción del empleo

Company Description

ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Computer Systems Compliance (CSC) (together, GxP). Founded in 2007, ADAMAS has focused on ensuring the highest standards of best practice are attained across the pharmaceutical sector. We serve an extensive global client base, including North America, Europe, and Asia Pacific, working with over 100 active clients and over 700 pharmaceutical companies, including 40 of the 50 largest global pharma and biotech firms.

At ADAMAS, our people are our primary asset. We possess the highest and broadest level of in-house knowledge, delivering genuine expertise globally. Our success is attributed to our talented team, and we offer competitive salaries, benefits, excellent working conditions, and opportunities for career development.

Job Description

1. Planning, preparation, conduct, reporting, and follow-up (including CAPA plans) of Pharmacovigilance (PV) audits according to quality standards and timelines.
2. Executing audits based on comprehensive understanding of regulatory requirements and GVP.
3. Performing GVP quality assurance projects for client companies within the pharmaceutical/biotechnology industry.
4. Assisting with business development activities.

Qualifications

• Experience in conducting and leading internal and external Pharmacovigilance audits for various stakeholders.
• Expert knowledge of national and international Pharmacovigilance legislation and guidelines.
• Proficiency in managing projects and ensuring timely delivery of results.
• Ability to identify issues and provide pragmatic solutions.
• Bachelor’s Degree in Life Sciences preferred.
• Willingness to travel up to 40% and conduct remote audits.

Additional Information

Why ADAMAS? We prioritize diversity, equity, and inclusion by fostering an equal opportunities workplace and a human-centric environment. Our organization values working together with a human-first approach, as our people are our greatest strength. We offer training and career development, a supportive work environment, and opportunities to collaborate globally. Our core values—Quality, Integrity & Trust, Drive & Passion, Agility & Responsiveness, Belonging, and Collaborative Partnerships—guide our operations.

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