About LawnStarter

LawnStarter is the nation's leading on-demand marketplace for lawn care and outdoor services, with over $100M in annual bookings. We connect homeowners with vetted local service professionals (Pros) who handle everything from weekly mowing to pool cleaning. We're profitable, growing 30%+ YoY, and expanding beyond lawn care to become the one-stop shop for all outdoor home services.

About the Pro Experience Team

Our marketplace only works when Pros succeed. We have 10,000+ active service providers across the country, and their quality directly determines whether customers stay or churn. The Pro Experience function owns everything that helps Pros get better at their jobs and more engaged with the platform—gamification, training, and the feedback loops that drive continuous improvement.

This is a new function. You'd be the first dedicated hire focused on Pro success and engagement.

The Role

You'll own the programs that help Pros progress from new signups to high-performing Gold and Platinum tier providers. This means designing and running gamification programs, building training initiatives, and partnering with Support to improve the Pro experience.

What makes this role different:

- You're building the function. You'll own it end-to-end and shape what Pro Experience means at LawnStarter.

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

The Data Quality Management role is essential in ensuring that our data meets the highest standards for quality and integrity throughout the research and pharmaceutical development process.

Main Activities:

About us:

Soar is a global fintech startup that specializes in financing and investment. Currently headquartered in Saudi Arabia, Soar is growing throughout the region with a mission to help people achieve their financial goals with innovative financial and property investment solutions and tools through its multi-purpose platform, designed to offer a simple and seamless user experience.

Role Overview

We are seeking a Senior Product Manager – Finance & Lending Systems to lead the strategy, design, and execution of Soar’s financial infrastructure. This role is responsible for the end-to-end product lifecycle of financing, payment, settlement, and reconciliation systems. The successful candidate will work at the intersection of lending, payments, regulatory compliance, and banking integrations within the Saudi market. The position requires strong expertise in regulated financial environments and the ability to translate complex financial and regulatory requirements into scalable product solutions.

Key Responsibilities

1. Product Strategy & Ownership

• Define and own the roadmap for financing and financial transaction systems.

• Align product initiatives with regulatory requirements and operational objectives.

À propos du poste

Rejoignez Excelya, où l'Audace, le Care et l'Énergie définissent qui nous sommes et la manière dont nous travaillons. Nous croyons en la création de solutions audacieuses et en un environnement inclusif, où la collaboration et le développement individuel avancent main dans la main.

Le poste est axé sur l'adaptation et l'application de techniques d'optimisation d'anticorps développées en interne aux projets de recherche en cours pour un de nos clients.

Missions principales

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Data & AI. You will play a critical part in driving innovation and making an impact in the clinical research space while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

À propos du poste

Rejoignez Excelya, où l'Audace, le Care et l'Énergie définissent qui nous sommes et la manière dont nous travaillons. Nous croyons en la création de solutions audacieuses et en un environnement inclusif, où la collaboration et le développement individuel avancent main dans la main.

Missions principales:

• Définir et mettre en œuvre la stratégie de biocompatibilité selon ISO 10993 et réglementations applicables (MDR, FDA si pertinent)
• Élaborer et maintenir le Biological Evaluation Plan (BEP) et le Biological Evaluation Report (BER)
• Identifier les essais nécessaires pour un dispositif implantable longue durée
• Assurer la cohérence scientifique et réglementaire de l’évaluation biologique
• Planifier, budgéter et suivre les activités d’essais
• Sélectionner et coordonner les laboratoires sous-traitants
• Superviser les échantillons de test avec les équipes R&D; et production
• Analyser et interpréter les résultats d’essais
• Rédiger et maintenir la documentation technique associée
• Contribuer au Technical Documentation / Design Dossier
• Garantir la conformité ISO 13485
• Contribuer aux investigations de non-conformités liées aux matériaux
• Renforcer le contrôle fournisseur sur les matières premières critiques
• Participer à l’amélioration continue du système qualité

Requirements

À propos du poste

Excelya recherche un(e) Ingénieur(e) Système avec une dominante software pour rejoindre un projet stratégique dans le domaine des dispositifs implantables cardiovasculaires.

Principales Responsabilités :

🔹 Ingénierie système & exigences

• Rédaction et structuration des exigences système et software
• Traduction des besoins utilisateurs en exigences techniques
• Gestion de la traçabilité des exigences
• Participation à l’architecture système (interaction hardware/software)
• Contribution aux revues de conception

🔹 Développement & conformité réglementaire

• Application du cycle en V
• Participation aux activités de Vérification & Validation (V&V)
• Contribution au Design History File (DHF)
• Travail en conformité avec :
• Règlement (UE) 2017/745
• ISO 13485
• ISO 14971
• IEC 62304

🔹 Gestion des risques

• Participation aux analyses de risques (AMDEC / FMEA / FTA)
• Analyse d’impact des modifications software

Requirements

Profil recherché :

À propos du poste
Rejoignez Excelya, où l’Audace, la Bienveillance et l’Énergie définissent qui nous sommes et notre manière de travailler. Nous croyons en la création de solutions audacieuses et en un environnement inclusif où la collaboration et le développement individuel vont de pair.

Cette opportunité vous permettra de contribuer à une équipe dynamique et ambitieuse en Opérations Cliniques. En tant qu’Attaché(e) de Recherche Clinique (Clinical Research Associate) chez Excelya, vous serez responsable du suivi de l’avancement des essais cliniques, du respect des exigences réglementaires et du soutien aux équipes sites afin de mener des recherches visant à améliorer les résultats pour les patients.

Responsabilités principales :

About the Job

Excelya is seeking an experienced International Regulatory Affairs Officer specializing in Advertising and Promotion. In this pivotal role, you will be part of a dedicated team that embodies Audacity, Care, and Energy, contributing to our mission of ensuring compliance and excellence in promotional practices across global markets.

Your expertise will drive the development and implementation of regulatory strategies for advertising and promotional materials, ensuring adherence to regulations across various international jurisdictions while aligning with our corporate goals.

Main Responsibilities:

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. As the Clinical Research Director for Inflammation and Immunology (I&I), you will lead critical clinical programs and play a pivotal role in advancing innovative therapies for patients.

This remote role empowers you to influence clinical strategy significantly, ensuring that we not only meet regulatory standards but also create optimal study designs that translate into successful patient outcomes.

Main Responsibilities: