QA & Deviations Specialist
il y a 2 semaines
Quality Consultant – Deviation Management Brussels Area, Belgium About Nalys Nalys is a fast-growing consultancy company specialized in high-tech engineering and life sciences. We partner with leading pharmaceutical organizations to deliver expert support and innovative solutions across a wide range of technical domains. At Nalys, we combine deep expertise with a human-centric approach — empowering our consultants to thrive and our clients to succeed. About the Role We are currently looking for a Quality Consultant to join one of our pharmaceutical partners for an on-site mission focused on deviation management within a GMP manufacturing environment. The consultant will play a key role in ensuring compliance and driving continuous improvement in quality processes. Responsibilities Manage deviations from end to end: identification, root cause analysis, implementation of immediate and preventive actions, and effectiveness checks Handle deviations of varying criticality: minor, major, and critical Communicate with external stakeholders regarding deviation investigations and resolutions Draft clear and concise technical documentation in English Collaborate closely with manufacturing, quality, and engineering teams Support audits and inspections related to deviation handling Promote a proactive and solution-oriented mindset within the team. Skills & Qualifications You hold a Master's degree in Engineering, Life Sciences, Pharmacy, or related field You have proven experience in deviation management within the pharmaceutical industry You understand perfectly GMP's and quality systems An experience in sterile manufacturing or aseptic filling is a strong asset You communicate fluently both in French and English A Lean Six Sigma Yellow or Green Belt certification is a plus Strong time management and organizational skills Team-oriented, proactive, and able to take initiative. Recruitment Process Olivia Braszko, Talent Acquisition Specialist at Nalys, will review your application and schedule an initial screening A technical interview will be conducted with our Technical Director Final validation will be done with our Business Unit Director, Jimmy Rousseaux, and the client.
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Senior Clinical Research Associate
il y a 2 semaines
Laeken, Belgique Planet Pharma Temps pleinPlanet Pharma are currently partnered with a global clinical research organisation and we are actively seeking a Senior CRA to join the business on a permanent basis, fully remotely in Belgium. Key Responsibilities: Monitor clinical trial sites to ensure studies are conducted according to protocol, Good Clinical Practice (GCP), and regulatory requirements....
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Quality Assurance Manager
il y a 4 semaines
Laeken, Belgique Barrington James Temps pleinAbout the Role Our client, a respected organisation operating in the Belgium, are currently recruiting a Quality consultant in the biotech space. The company is committed to delivering high-quality, innovative healthcare solutions and maintaining the highest standards of compliance with regulatory requirements. This is an excellent opportunity to join a...
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Freelance/Contract Responsible Person
il y a 2 semaines
Laeken, Belgique ProPharma Temps pleinCompany profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world's largest RCO (Research Consulting Organization),...
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Test Engineer
il y a 4 semaines
Laeken, Belgique CST Advisory Temps pleinFor a leading international technology-driven organization We are looking for a Freelancer Senior Test Engineer to join a major international technology & digital innovation organization in Belgium. Only candidates residing in Belgium will be considered. About the Role As a Senior Test Engineer, you will support the quality assurance activities across...
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(H/F) Test Automation Specialist
il y a 17 heures
Laeken, Belgique speos Temps pleinSenior Automation Software QA Tester Mission As Senior Automation Software QA Tester, you realize tests according to the department procedure and following test plan. You also suggest improvement for the Testing methodology, and you maintain non regression test cases for client application and products. Responsibilities As Senior Automation Software QA...
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Engineer QA Operational
il y a 4 semaines
Laeken, Belgique Prothya Biosolutions Temps pleinAbout the Company Prothya Biosolutions makes life-saving plasma medicines and is proud of that! Every day, Prothya colleagues take the extra mile to improve the health of millions of patients worldwide. Are you looking for a position at a flexible and fast-growing company with an exciting history? At Prothya you can count on an attractive, safe and...
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Engineer QA Operational
il y a 7 jours
Laeken, Belgique Prothya Biosolutions Temps pleinAbout the Company Prothya Biosolutions makes life-saving plasma medicines and is proud of that! Every day, Prothya colleagues take the extra mile to improve the health of millions of patients worldwide. Are you looking for a position at a flexible and fast-growing company with an exciting history? At Prothya you can count on an attractive, safe and...
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Commissioning, Qualification and Validation Engineer
il y a 3 semaines
Laeken, Belgique Nalys Temps pleinCQV Engineer – Senior Level Brussels, Belgium About Nalys Nalys is a fast-growing consultancy company specialized in high-tech engineering and life sciences. Founded 15 years ago, we partner with leading organizations to deliver innovative solutions and expert support across a wide range of technical domains. At Nalys, we believe in combining deep...
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Senior Clinical Research Associate
il y a 17 heures
Laeken, Belgique Planet Pharma Temps pleinSenior Clinical Research Associate Belgium | Remote | Permanent A global clinical research organisation is hiring a Senior Clinical Research Associate to support oncology clinical trials in Belgium This is a remote, permanent opportunity offering autonomy, responsibility, and involvement in complex, science-driven studies. The Role Lead site monitoring...
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Senior Clinical Research Associate
il y a 2 semaines
Laeken, Belgique Planet Pharma Temps pleinTitle: Senior Clinical Research Associate Company: Global Leading CRO Location: Remote - Belgium Our client is seeking an experienced CRA II or Senior CRA with strong oncology experience to take full ownership of 1–2 clinical protocols. This role goes beyond traditional monitoring, encompassing contract negotiation, start-up activities, monitoring, and...
