ALSINOVA CRO

Alsinova provides end-to-end life science research services that combine medical expertise with AI-driven tools. As a non-clinical and clinical research company, Alsinova uses a Digital CRO approach, data science, automation, and machine learning to deliver RWE, regulatory affairs, and vigilance support. It operates across 26 countries with flexible collaboration models. Supported by AI and human experts, it tailors solutions for pharma, biotech, and medical device clients. The company targets global life science programs with scalable partnerships.

BioEquivalenceBiostatisticsClinical Data FabricClinical OperationsClinical Project ManagementClinical ResearchConsultingData ManagementData SciencesDecentralized Clinical TrialsDigital EnablementeHealthFSPLife SciencesMedical WritingPhase I to IVQuality AssuranceRegulatoryRWESafetyVigilancealsinova.com

ALSINOVA CRO

HQBoulogne-Billancourt, FR

Team Size216

Open Jobs69

Total Funding-

Latest FundraiseUnknown

Join the Team

Quality Assurance Specialist – QMS - Paris, France (F/M)

HybridParis, Île-de-, FR

Hybrid • Paris, Île-de-, FR

What We Will Accomplish Together Alsinova, the CRO subsidiary of the Astek Group, is looking for its next Quality Assurance Specialist to support and improve Quality Management Systems (QMS) for key projects in the life sciences sector.

Your Mission (should You Decide To Accept It) Reporting to the Quality Manager and working closely with cross-functional teams, you will support and develop QMS processes in compliance with applicable regulations (GxP, ISO standards, etc.).

You’ll contribute to the continuous improvement of the quality system and ensure proper implementation across departments and projects.

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TL;DR

Company Overview

Funding Track Record

Founders

What we do

ALSINOVA CRO

HQBoulogne-Billancourt, FR

Team Size216

Open Jobs69

Total Funding-

Latest FundraiseUnknown

Join the Team

Quality Assurance Specialist – QMS - Paris, France (F/M)

HybridParis, Île-de-, FR

Hybrid • Paris, Île-de-, FR

You’ll contribute to the continuous improvement of the quality system and ensure proper implementation across departments and projects.

Teeming tracks opportunities at over 24,000 AI startups, then works with you to find (and land) the one you'll love.

Mobile Developer

ContractHamburg, DE

Contract • Hamburg, DE

Data Scientist

ContractNew York, US

Contract • New York, US

Product Designer

InternshipRotterdam, NL

Internship • Rotterdam, NL

Frontend Developer

InternshipNiš, RS

Internship • Niš, RS

Mobile Developer

InternshipNovi Sad, RS

Internship • Novi Sad, RS

Mobile Developer

ContractBelgrade, RS

Contract • Belgrade, RS

Your Daily Activities Will Be

Ensure the proper deployment and maintenance of the Quality Management System
Write, update, and manage quality documentation: procedures, instructions, forms
Organize and follow-up on internal and external audits
Manage deviations, CAPAs and change control processes
Monitor and report quality indicators and KPIs
Contribute to training plans and awareness campaigns on quality standards
Support qualification and validation activities (equipment, processes, suppliers)
Ensure compliance with applicable regulatory frameworks (GMP, ISO 9001/13485...)
Participate in the continuous improvement of the system

Your Future Team You’ll be part of a motivated and quality-driven environment that encourages initiative, process optimization and proactive collaboration.

You’ll benefit from technical support, cross-functional exposure, and career development opportunities within a fast-growing organization.

You PharmD or Master's degree (Bac+5) in Quality Assurance, Pharmaceutical Affairs, or a scientific field

Minimum of 3 years’ experience in Quality Assurance, with a strong focus on Quality Management Systems (QMS)
Solid knowledge of regulatory standards: GMP (Good Manufacturing Practices), ISO 9001, ISO 13485, etc.
Hands-on experience in documentation management, deviation handling, CAPA, and change control
Prior involvement in quality audits (internal and/or external)
Comfortable working with QMS tools (e.g. Veeva Vault, eQMS platforms)
Excellent written communication skills and strong attention to detail
Organized, autonomous, proactive, with a strong team spirit and collaborative mindset
Fluent English and French, both spoken and written

Our Benefits Rejoindre Astek, c'est choisir :

un accélérateur d’expérience, où chaque mission est une opportunité de progresser
un accès à une multitude de projets techniquement passionnants pour nos clients comme en interne
un accompagnement de proximité individualisé pour un parcours professionnel sur mesure
un apprentissage continu, grâce à notre Académie de formation interne
un environnement de travail convivial et inclusif, soutenu par des pratiques RH certifiées #TopEmployer2025 Let's move forward.

We Base Our Relationships On

Respect for employees and clients, and their aspirations,
Personalized support for employees and clients,
Regular career management,
Transparent communication,
Constant responsiveness, availability, and attentiveness.