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Isalys Life Sciences

Validation Qualification Engineer in the pharmaceutical industry M/F

Validation Qualification Engineer in the pharmaceutical industry M/F

Paris, France

13 Mar 2025

our method of excellence

Ambition and development

Our development plan for 2025 – 2030 aims to exceed €115 million in revenue by the end of 2030, with an ISA team of over 750 engaged and committed members working to elevate each subsidiary to the highest level.

Job Description and Missions

As a consultant in qualification/validation in the pharmaceutical industry, you will be involved in the production of liquid medicines (injectable/sterile) through the following missions:

  • Qualification of pharmaceutical production equipment

  • Drafting protocols, functional analyses, and qualification reports

  • Carrying out Qualification operations (QI, QO, QP)

  • Managing non-conformities; participation in investigations

  • Working in collaboration with production, engineering, and development services

Desired Profile

Pharmacist, Engineer, Bac+5, you have applied your skills in a pharmaceutical industrial context during a significant experience or during internships.

Are you motivated by the dynamics of projects and the discovery of a diversity of human, methodological, and technical environments?

We are based in the heart of Paris with several potential projects across France. Our motto is entrepreneurship and friendliness.

So don’t wait any longer, join us!

Useful Information

  • Location Strasbourg - 67, France - area of travel: national

  • Contract CDI

  • Salary 30000.00 to 50000.00 EUR per year

  • Qualification Level Engineer/Manager/Bac +5

  • Experience 1 to 7 years

  • Working Conditions Full-time

  • Function Engineering - Chemistry/Pharmacy/Bio, Quality/Hygiene/Safety/Environment

  • Sector Pharmaceutical/Biotechnology/Chemistry Industry, Business Services

  • Remote Work No remote work

 What do we offer? 

  • Joining a team committed to service quality and the success of assigned projects

  • A diversity of environments, contexts, and topics to be challenged and grow

  • The opportunity to be a key player in flagship projects of the pharmaceutical industry with the largest laboratories, CDMO, and biotechs

  • Individual support and follow-up to achieve your professional project

  • Mentoring with ISA Experts and training to enhance your skills

  • A group where performance and well-being, development and CSR work together

  • A friendly corporate life where everyone is valued and has their place, where internal networking and mutual assistance are encouraged

  • Afterwork & regular events to ease your integration and develop your ISA network in a relaxed atmosphere

Your compensation will consist of a fixed salary, determined based on your seniority and responsibilities as an ISA Consultant, a commission plan, and legal social benefits.

We are well aware that remote work is essential. However, the role of an ISA consultant requires human interactions, idea exchanges, and experience sharing. The client site remains the preferred place to achieve this. After an integration period, occasional remote work may be possible depending on your role and the projects undertaken.

Interested?