Why Join Us?
At Excelya, we are committed to excellence in healthcare, and we invite you to be part of our dedicated team where your expertise can make a significant impact.
As a young, ambitious health company with over 900 talented professionals, we strive to be Europe’s leading mid-size CRO, delivering the best employee experience. Our integrated service model enables you to engage in diverse projects, working alongside industry experts to enhance scientific knowledge and improve the patient journey.
About the Job
We are seeking an Expert in Quality Assurance for Injectables and Barrier Technology to strengthen our commitment to delivering high-quality products. In this pivotal role, you will lead quality assurance processes, ensure regulatory compliance, and drive continuous improvement initiatives.
Main Activities:
- Managing task lists and interacting with other peripheral streams (maintenance, logistics, etc.)
- Communicating tasks to the project manager daily and via monthly KPIs. Tasks and deliverables for the project and authorities:
- Risk analyses (initiation, execution, conclusion, action plan)
- Drafting quality documents (test protocols/plans and reports, standard operating procedures, operating procedures) • GAP analysis against GMP (Appendices 1, 13)
- Scientific justification (documents) for deviations from regulatory requirements
- Monitoring action plans, investigations, and evaluation of out-of-specification (OOS) results.
Requirements
About You
We are looking for candidates who embody our values of Audacity, Care, and Energy:
- Experience: A minimum of 5 years of experience in quality assurance in the pharmaceutical or biotech industry, with a focus on injectables under isolator and barrier technology.
- Skills: Strong knowledge of regulatory requirements (GMP, ISO) and quality assurance methodologies. Excellent analytical and problem-solving abilities.
- Education: Master’s degree in Life Sciences, Pharmacy, or a related field.
- Languages: Proficient in English and French; other languages are a plus.
- Fluency in French and English is required.
Benefits
Why Join Us? At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare. Here’s what makes us unique We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey. Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
Top Skills
What We Do
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of Full-service CRO, FSP, and Resourcing solutions guided by compassion, care, and excellence.
Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.
