Non-clinical Quality Assurance Leader

**Part-time / Consultant**: - Published on 14/03/2024_ **Responsibilities**: - Contribute to meet GLP regulatory compliance for the Test Facility (OECD guidelines). - Ensure implementation of processes and systems (e.g. facilities, equipment, personnel, methods, practices, records) according to the GLP non-clinical program of the Test Facility. - Support...

Overview: This internship is intended to provide you an elementary understanding of all areas of clinical operations, with a focus on study conduct and data collecting in prospective clinical studies. You will also be able to learn the basics of quality assurance and good clinical practice (ICH-GCP). You will be teamed with two clinical study or clinical...

**Fonction**: The Institut Jules Bordet is an integrated multi-disciplinary centre, unique in Belgium and with an international reputation. The hospital is an academic non-for-profit organisation devoted entirely to patients affected by cancer. The Clinical Trials Support Unit (CTSU) is a department of the Institut Jules Bordet and fights cancer through the...

**Site Name**: USA - Maryland - Rockville, Belgium, Italy **Posted Date**: May 11 2023 Are you energized by an opportunity to accelerate and deliver a Clinical Sciences Strategy that drives compliance and efficiency? If so, this Associate Director, Clinical Sciences Lead (CSL) role could be an exciting opportunity to explore. Innovation is the beating...

**Allianz Partners** is the world leader in travel insurance, roadside assistance and personal services, every day is a new opportunity to make a difference. We are proud of our 17,000 employees spread across 6 continents in 34 countries and speaking 40 languages. For as many different scenarios as there are people, we’re here to help our customers out of...

Elaboration and maintenance of information systems quality control procedures. - Create quality measurements/KPIs to track improvements in products/solutions. - Provision of quality plans and service level agreements. - Information Systems quality control and evaluation. - Provision of quality studies, quality assessments or other quality matters associated...

**POSITION TITLE**: Senior Clinical Research Associate **DEPARTMENT**:Ora Europe **LOCATION**: Remote, Belgium **Ora Values the Daily Practice of ** - Prioritizing Kindness - Operational Excellence - Cultivating Joy - Scientific Rigor_ At Ora, we are building the future of ophthalmic clinical research. As the world's leading full-service ophthalmic drug...

Company Overview: As a key division of the SASMAR group, a renowned provider of medical devices and food supplements worldwide, we are committed to upholding the highest standards of quality and regulatory compliance. Our products adhere to global regulatory requirements, including ISO 13485, ISO 9001, FDA guidelines, and other relevant regulations across...

**Function**: Are you looking to take your **next career step in Quality Assurance?** As our** Quality Assurance Manager, you will be 100% responsible for**: - **Leading and managing** the Quality Assurance Department **in day-to-day activities and taking full ownership for **EMVO’s Quality Management System.**: - **Ensuring** the legal, quality...

**Company Description** Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Clinical Data Coordinator in Belgium. **Job Overview** - Ensuring data is entered into...

Amador Bioscience is a next-generation provider of translational research and clinical development solutions. As a global contract research organization (CRO) with established sites in the United States, Europe, and China, Amador confidently meets international clinical trial quality and compliance standards. **Position Summary** The Incumbent is an...

Amador Bioscience is a next-generation provider of translational research and clinical development solutions. As a global contract research organization (CRO) with established sites in the United States, Europe, and China, Amador confidently meets international clinical trial quality and compliance standards. **Position Summary** The Incumbent is an...

At Uni Systems, we are working towards turning digital visions into reality. We are continuously growing and we are looking for a Quality Assurance Manager to join our UniQue Brussels team! What will you be bringing to the team? - Provision of quality plans and service level agreements. - Elaboration and maintenance of IS quality control procedures. - IS...

A global diagnostics firm based in Belgium is hiring a Quality Assurance professional for Paternity Cover. Reporting to the Head of Compliance and working in an important role, you will be given full autonomy and exposure to a variety of tasks. **In this position, you will**: Be responsible for covering all compliance and quality assurance responsibilities...

**Location**: Belgium - Home or office based **Schedule**: Permanent, Full-time Do you want to join a team that is passionate about making a difference in drug and medical device development? CROMSOURCE, a growing CRO, is recruiting for a Project Manager to join their clinical operations team. This is a permanent opportunity in Belgium. You will work on...

As the Right Hand, you will play an important role in ensuring compliance with pharmaceutical certification standards and our quality system, conducting audits in the different abroad manufacturing sites, and collaborating with various colleagues from different department and across different specialties and levels. Your **main** **responsibilities** are as...

**Brief Description** The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager, the person - ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally...

**Brief Description** The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager, the person - ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally...

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. **At our core, we exist to create products that seek to improve the quality of life for people living with...

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. **At our core, we exist to create products that seek to improve the quality of life for people living with...