Pierre Fabre Pharmaceuticals Inc.
Responsable du Pôle Qualité et Validation des SI- CDI- H/F
Pierre Fabre Pharmaceuticals Inc. - Iowa, Louisiana, United States, 70647
Work at Pierre Fabre Pharmaceuticals Inc.
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Overview
Responsable du Pôle Qualité et Validation des SI - CDI - H/F
Apply locations: Tarn (81) | Time type: Full time | Posted on: Posted 2 Days Ago | Job requisition id: JR108084 Who we are? Pierre Fabre is the 2nd largest dermo-cosmetics laboratory in the world, the 2nd largest private French pharmaceutical group, and the market leader in France for OTC products sold in pharmacies.
Our portfolio includes medical franchises and international brands such as Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, René Furterer, A-Derma, Naturactive, and Pierre Fabre Oral Care.
Established in Occitanie, with over 95% of products manufactured in France, the Group employs around 10,000 people worldwide, distributing products in about 130 countries. 86% of the Group is owned by the Pierre Fabre Foundation, with the remainder owned by employees via an employee stock ownership plan.
In 2019, Ecocert Environment awarded the Group the "Excellence" level for its CSR approach according to ISO 26000. Forbes recognized Pierre Fabre as one of the "World's Best Employers 2021," ranking top in cosmetics and top 10 in pharmaceuticals globally.
Your mission Passionate about quality, compliance, and technological innovation with a modern view on IT challenges?
Join the Digital Acceleration Information System (DAIS) as
Responsable du Pôle Qualité & Validation des SI
to lead, structure, and grow a team of 4, managing a service center.
This strategic role is based in Castres (81), at the heart of Pierre Fabre's digital transformation.
You will bring a fresh perspective to quality practices and challenge existing models to evolve them.
Your role within a pioneering and expanding company:
Ensure regulatory compliance and quality of the Group's information systems. Be a key player in our modernization efforts.
Lead the adaptation of quality practices in a transforming environment (Cloud, SaaS, FinOps, AI).
Rebuild a dynamic team fostering continuous improvement and innovation.
Act as the primary contact for quality authorities and regulatory bodies.
Detailed Responsibilities
Define and lead the quality roadmap for DAIS, following Group Quality directives and market standards.
Develop and monitor Quality, Regulatory, and Compliance indicators.
Represent Quality and SI Validation internally and in group quality committees.
Maintain awareness of applicable standards (ITIL, GAMP5, etc.) and ensure operational implementation.
Establish and oversee the quality system structure, processes, and continuous improvement initiatives.
Promote and support teams in adhering to quality and validation regulations, including training.
Manage validation, change management, deviations, audits, and corrective actions for regulated SI.
Represent and coordinate audits and inspections by clients, suppliers, and authorities (FDA, EMA, etc.).
Lead and manage the Quality & Validation teams.
Manage the budget for your scope or delegate activities as appropriate.
This role allows telecommuting up to 2 days per week after the probation period.
We offer attractive compensation packages including incentives, participation, employee stock plans, health and insurance benefits, RTT, transportation allowances, and a vibrant employee engagement program.
Who you are? With a Bac +5 or equivalent, you have proven experience in Quality and Validation of Information Systems within a regulated environment. Fluent in English, familiar with project management and lifecycle methods, and ideally from sectors demanding high quality standards such as pharmaceuticals, nuclear, or aerospace.
We believe diversity fosters fulfillment, social balance, and complementarity among our employees, and we welcome applications from all backgrounds.
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Apply locations: Tarn (81) | Time type: Full time | Posted on: Posted 2 Days Ago | Job requisition id: JR108084 Who we are? Pierre Fabre is the 2nd largest dermo-cosmetics laboratory in the world, the 2nd largest private French pharmaceutical group, and the market leader in France for OTC products sold in pharmacies.
Our portfolio includes medical franchises and international brands such as Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, René Furterer, A-Derma, Naturactive, and Pierre Fabre Oral Care.
Established in Occitanie, with over 95% of products manufactured in France, the Group employs around 10,000 people worldwide, distributing products in about 130 countries. 86% of the Group is owned by the Pierre Fabre Foundation, with the remainder owned by employees via an employee stock ownership plan.
In 2019, Ecocert Environment awarded the Group the "Excellence" level for its CSR approach according to ISO 26000. Forbes recognized Pierre Fabre as one of the "World's Best Employers 2021," ranking top in cosmetics and top 10 in pharmaceuticals globally.
Your mission Passionate about quality, compliance, and technological innovation with a modern view on IT challenges?
Join the Digital Acceleration Information System (DAIS) as
Responsable du Pôle Qualité & Validation des SI
to lead, structure, and grow a team of 4, managing a service center.
This strategic role is based in Castres (81), at the heart of Pierre Fabre's digital transformation.
You will bring a fresh perspective to quality practices and challenge existing models to evolve them.
Your role within a pioneering and expanding company:
Ensure regulatory compliance and quality of the Group's information systems. Be a key player in our modernization efforts.
Lead the adaptation of quality practices in a transforming environment (Cloud, SaaS, FinOps, AI).
Rebuild a dynamic team fostering continuous improvement and innovation.
Act as the primary contact for quality authorities and regulatory bodies.
Detailed Responsibilities
Define and lead the quality roadmap for DAIS, following Group Quality directives and market standards.
Develop and monitor Quality, Regulatory, and Compliance indicators.
Represent Quality and SI Validation internally and in group quality committees.
Maintain awareness of applicable standards (ITIL, GAMP5, etc.) and ensure operational implementation.
Establish and oversee the quality system structure, processes, and continuous improvement initiatives.
Promote and support teams in adhering to quality and validation regulations, including training.
Manage validation, change management, deviations, audits, and corrective actions for regulated SI.
Represent and coordinate audits and inspections by clients, suppliers, and authorities (FDA, EMA, etc.).
Lead and manage the Quality & Validation teams.
Manage the budget for your scope or delegate activities as appropriate.
This role allows telecommuting up to 2 days per week after the probation period.
We offer attractive compensation packages including incentives, participation, employee stock plans, health and insurance benefits, RTT, transportation allowances, and a vibrant employee engagement program.
Who you are? With a Bac +5 or equivalent, you have proven experience in Quality and Validation of Information Systems within a regulated environment. Fluent in English, familiar with project management and lifecycle methods, and ideally from sectors demanding high quality standards such as pharmaceuticals, nuclear, or aerospace.
We believe diversity fosters fulfillment, social balance, and complementarity among our employees, and we welcome applications from all backgrounds.
#J-18808-Ljbffr