Nieuwe vacatures per e-mail ontvangen.
- ...Fonction Jouw verantwoordelijkheden Valideren van interne IRB-modellen en beoordelen van hun kwaliteit, nauwkeurigheid en robuustheid... ...en te valideren in plaats van te bouwen? Dan is deze rol als Quantitative Risk Validation Manager de perfecte volgende stap....AanbevolenThuiswerk
- ...van de rol is tweeledig: De basis blijft stevig: het valideren van interne IRB-modellen (PD, LGD, EAD) . Je toetst aannames... ...vorm te geven. Job details Ben je vandaag IRB-modeller of validator en merk je dat je werkveld te smal wordt? Wil je je expertise...AanbevolenThuiswerk
- ...Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual... ...analytical laboratory plays a key role in the development and validation of analytical methods to characterize drugs and to perform quality...AanbevolenMet contract
4500 € - 6000 € per maand
...Our client, an established but also growing company in the pharmaceutical sector, is looking for a Regulatory Affairs and Pharmacovigilance... ...partnerships and professional growth. Approve regulatory validation of local artwork, product characteristics, patient...AanbevolenFulltime- ...discover the world of intellectual property (IP): learn how to validate new inventions, gain hands-on-experience in drafting and... ...focuses on basic science and translating scientific results into pharmaceutical, agricultural and industrial applications. VIB’s Innovation &...AanbevolenStage
- ...responsible for providing quality oversight for computer system validation activities in accordance with Janssen policies standards... ...degree or equivalent experience. ~3 years experience in the pharmaceutical industry. ~ Knowledge of cGMP/CSV compliance (21 CFR Parts;...AanbevolenFulltime
- ...integrity and regulatory compliance requirements. Partner with validation and quality teams to ensure readiness for audits and... ...identify and evaluate new technologies that can be applied to Pharmaceutical Supply Chain/Quality. Ability to communicate technical concepts...AanbevolenFulltime
- ...with at least 3 years of cross-functional experience in the pharmaceutical industry. Pharmaceutical Knowledge: In-depth understanding... ...of pharmaceutical product development qualification packaging validation testing release and distribution processes. Regulatory Knowledge...AanbevolenFulltimePloegendienstWeekendwerk
- ...collaborate cross functionally with engineering maintenance validation and operation teams to ensure all systems and processes meet... ...in engineering with chemistry or analytical background or in pharmaceutical sciences. At least 5 years of relevant QA or Qualification...AanbevolenMet contractFulltime
- ...CMC documentation (e.g. process development protocols/reports validation protocols/reports stability protocols/reports etc.) and batch... ...cycles. Qualifications: Masters / PhD in chemistry pharmaceutical sciences bioengineering or other discipline within...AanbevolenFulltimeStage
- ...voorafgaand aan de development teams zodat je input kan doorstromen naar de ontwikkeling. Na de ontwikkeling kan je de functionaliteiten valideren d.m.v. testing en controle. Je werkt intens samen met de verschillende spelers in een project team zoals product owners, project...AanbevolenZZP
IT-Planet
Gent7 dagen geleden - ...meets its pre-determined specifications by deploying process validation process system engineering data architecture and continuous process... ...the ability to work well under pressure Experience in the Pharmaceutical Biotechnology Cell Therapy human plasma derived products or...AanbevolenFulltime
- ...solutions Optimize for performance, latency, power consumption, and reliability Support system bring-up, debugging, and validation on real Hardware Contribute to documentation and engineering best practices in a safety-critical environment...Aanbevolen
Vivid Resourcing
Gent14 dagen geleden - ...Are you looking for a dynamic role in a fast-growing biotech company? Do you have experience in a warehouse environment within a pharmaceutical company or are you someone who works very accurately and seeks variation between physical and administrative work? Keep reading...AanbevolenMet contractFulltimePloegendienstWeekendwerk
- ...strategic research institute in life sciences that focuses on fundamental science aa well as translating scientific results into pharmaceutical agricultural industrial and societal applications. VIB is funded by the Flemish government and works in close partnership with...AanbevolenFulltime
- ...with at least 5 years of cross-functional experience in the pharmaceutical industry. Pharmaceutical Knowledge: In-depth understanding... ...of pharmaceutical product development qualification packaging validation testing release and distribution processes. Regulatory Knowledge...FulltimePloegendienstWeekendwerk
4500 € - 5500 € per maand
...Our client, a growing pharmaceutical company, offers an exciting opportunity for a QA Manager to be responsible for the BeLux region. This company became a bigger global structure last year and bought extra products into the already diverse portfolio, so they expanded...Fulltime- ...Biomedical Engineering Bioengineering Biotechnology Biomedical Sciences Chemical Engineering Industrial Engineer Bioinformatics Pharmaceutical Sciences Chemistry etc.) Background or exposure in Data Science Bioinformatics Robotics Mathematics Statistics or Physics is...FulltimeStage
- ...alarm management. Safety is fundamental and work permit management is the foundation of all our activities. As we are working in a pharmaceutical company/environment quality management is fully interwoven and indispensable in everything we do. Technical expertise in...FulltimeStageVoor uitvoerders
- ...minimum of a Bachelors Degree in Engineering Science or an equivalent technical field. Experience in the biological and/or pharmaceutical industry with relevant micro experience related to manufacturing. Aseptic processing in an ISO 5 cleanroom and biosafety cabinets...Met contractFulltime
- ...About You: Bachelors or masters degree in Life Sciences Pharmacy Medicine Business or related field. Minimum 58 years of pharmaceutical sales experience with at least 2 years in a leadership or field coaching role. Proven track record in specialty areas ideally...Fulltime
- ...tastings are everywhere in Belgium) Fluent Dutch speaking. French is a BIG plus for events/tastings in Brussels Preferred to have a valid driving licence. Able to work in any social setting, alone or team setting. ESSENTIAL PERSONAL REQUIREMENTS As a Student...Met contractWeekendwerk
Yugen bvba
Gent12 dagen geleden - ...work-life balance! Requirements: Fluency in Dutch (C1 level) and good English skills (B1+) EU citizenship or valid work permit in Portugal Problem-solving mindset, motivation to learn, and team spirit Want to experience life in Portugal...
- ...work one sprint prior to the development teams so that your input can flow through to the development. After development you can validate the functionalities through testing and checking. You work closely with the various players in a project team such as product...Fulltime
- ...conquering the world, right? If this sounds like you, let’s see if you tick these boxes: You are currently living in Belgium You hold a valid certificate as a construction site machinist You operate a crane smoothly—whether with caterpillar tracks or wheels You...FulltimeParttime
- ...actionable development tasks. Your role is essential in refining our product backlog using SCRUM methodologies defining roadmaps and validating features to meet user requirements. What will you do Utilize your domain and technical knowledge to bridge the gap...FulltimeCDD
- ...relevant scientific or business field Minimum of 3 years of experience in alliance management or a related role within the pharmaceutical or biotechnology industry Proven track record of successfully managing strategic partnerships or collaborations with external...FulltimeStage
- ...Fluent in English our working language. Education Experience and Qualifications Masters degree or PhD in biotechnology pharmaceutical sciences or bioengineering with relevant expertise in CMC development and CMC regulatory dossier development (IND/IMPD/BLA/MAA)...FulltimeStage
- ...experience in Regulatory Affairs (dossier preparation & submission compliance GMP ISO manufacturing and quality control of chemicals or pharmaceutical products) Minimum of 1-3 years experience in registration submission in Europe and/or other regions Ability to work...Met contractFulltimeThuiswerk
- ...in a team. Competencies in the job… Do you have experience as a Driver C? Do you have a digital driver card and code 95 and a valid medical certificate? Are you willing to work more than 8 hours a day and are you flexible in terms of hours? Can you start up...
