CONSULTYS

About the Company

CONSULTYS is a global engineering and services consulting company exclusively dedicated to the bio industry.
Since 2005, Consultys has been working with some of the most sophisticated, innovative and successful bio industries on their technical projects.

Our 600 consultants are working on innovative projects in engineering, production, quality (QA, QC, validation), R&D and regulatory affairs across Belgium, Switzerland, Germany and France. Using this experience, CONSULTYS has helped the manufacturers in all stages of drug development.

We are as passionate about the technological challenges as by the human adventure. We truly believe in proximity management so that our consultants can develop technical competencies in a pleasant environment.
Respect, transparency and performance these are the values that have made CONSULTYS one of the most high-performing biotech consulting companies.

Do you want to integrate a human-sized company that values the individual and the performance? Do you want to invest in long-term innovative projects? To share your skills in a close-knit team where experiences are shared freely? So, join us!

We offer you an attractive salary and fringe benefits. You will work in a stimulating environment, with opportunities for personal development.

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CONSULTYS, la reference du conseil en Ingenierie 100% Life Sciences !

Vous vous demandez si il est aise de concilier vie professionnelle et vie personnelle?
Chez CONSULTYS nous vous repondons OUI !

- Pas de clause de mobilite, garantie de travailler a proximite de chez soi
- Projets d'une duree moyenne d'1 an a 18 mois
- Recrutement 100% CDI : stabilite
- Projets en accord avec les souhaits d'evolution dans l'industrie Life Sciences

Votre futur commence ici -> rejoignez l'avenir du conseil pharmaceutique et biotechnologique!

L'equipe Recrutement se tient disponible pour echanger:

recrutement@consultys.fr

Listed Jobs

Company Name

CONSULTYS

Job Title

Project Management Officer (PMO) - Région Lyonnaise F/H

Job Description

**Job title:** Project Management Officer (PMO) **Role Summary:** Provide central oversight and support for project execution across the organization, ensuring accurate tracking, reporting, and continuous improvement of project management processes. **Expectations:** Deliver reliable project data and insights to enable decisions by senior leadership, support project teams with planning and resource management, and actively drive process optimization. **Key Responsibilities:** - Deploy and maintain project tracking tools (planning, budgeting, KPI dashboards). - Coordinate activities between project teams and internal/external stakeholders. - Prepare and lead steering committee meetings; produce minutes and monitor action items. - Consolidate project reporting, guaranteeing data accuracy for status, risks, and costs. - Identify and implement improvements to project management methods, tools, and procedures. - Assist project managers with resource planning and scheduling. **Required Skills:** - Proficiency with planning and reporting tools (MS Project, advanced Excel, Power BI). - Strong analytical, organizational, and rigorous data management capabilities. - Fluent in professional English (written and spoken). - Knowledge of project management methodologies (PMI, Prince2, Agile). **Required Education & Certifications:** - Minimum Bac+5 (5‑year degree) in project management, engineering, or equivalent field. - Relevant certifications (e.g., PMI‑PMP, Prince2, Certified ScrumMaster) preferred.

Lyon, France

On site

14-01-2026

Company Name

CONSULTYS

Job Title

Chargé(e)s de validation des systèmes informatisés - Nice

Job Description

Job Title: Computerised Systems Validation Officer Role Summary: Conduct end‑to‑end validation of pharmaceutical IT systems, ensuring compliance with regulatory standards (GAMP5, ALCOA, BPF/GMP). Draft validation documentation, execute tests, and manage data integrity throughout the system lifecycle. Expectations: Apply expertise in GAMP5, ALCOA, BPF/GMP, Siemens and Schneider technologies, and ERP/MES platforms. Maintain professional English proficiency, exhibit diligence, responsiveness, and precision. Key Responsibilities: - Develop validation plans and reports for computerized systems. - Execute validation and performance tests. - Draft Quality Improvement (QI) and Quality Operations (QO) protocols. - Ensure adherence to data integrity principles (ALCOA, BPF/GMP). - Coordinate with cross‑functional teams to maintain documentation and system records. - Review and update validation artefacts as systems evolve. Required Skills: - Strong knowledge of GAMP5, ALCOA, BPF/GMP, and pharmaceutical data integrity. - Proficiency with Siemens, Schneider automation, ERP and MES environments. - Test design, execution, and documentation skills. - Excellent written and verbal communication in English. - Detail‑oriented, proactive, and able to manage multiple priorities. Required Education & Certifications: - Bachelor's or Master's degree in Engineering or equivalent (Bac +5). - Minimum of 1–2 years’ experience in data integrity within a pharmaceutical setting.

Nice, France

On site

13-02-2026