September 4, 2023
Published by Joachim Nuyttens at September 4, 2023
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Setting your own career priorities

At Trevalco, we believe that everyone’s career path is unique, and our goal is to provide a supportive environment where our employees can discover their best way forward. Whether you’re just starting out in your career or you’re an experienced professional, we offer various opportunities to help you grow and develop. We also understand that work is just one part of a fulfilling life. Your priorities might shift from career development and promotion, to more focus on family life, health […]
June 29, 2023
Published by Joachim Nuyttens at June 29, 2023
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Employee testimonial – Elke Weyenbergh

Our colleague Elke talks about what it’s like to work for Trevalco as a consultant specializing in Quality Assurance (QA). What are your main duties as a consultant in QA? “QA ” within the pharmaceutical industry is a very broad concept, in the team at the customer we are mainly concerned with following up projects. This can involve modifications to existing production lines/rooms/processes as well as the installation of a completely new line, whether in a new building or not. […]
February 9, 2023
Published by Joachim Nuyttens at February 9, 2023
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From lab to life: AI trends in the Life Science industry

by Tom Oostvogels, Jr. Consultant at Trevalco Artificial Intelligence (AI) is all around us nowadays and it is starting to transform industries in all sectors. As such, AI is also finding its way to the life science industry and will help healthcare as we know it. The incorporation of Artificial Intelligence in life sciences has opened doors to new possibilities and has created new opportunities for innovation and growth. In this post, we’ll explore 5 of the latest trends in […]
February 1, 2023
freelance consultant in de farmaceutische industrie
Published by Joachim Nuyttens at February 1, 2023
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Working as a freelance consultant in the pharmaceutical industry

The pharmaceutical industry is a dynamic and rapidly growing sector that is increasingly hiring freelance consultants for temporary projects. As a freelance consultant in the pharmaceutical industry, you can work on challenging projects and improve your skills while setting your own schedule and creating your own work environment. Benefits of working as a freelance consultant in the pharmaceutical industry: It is also important to choose the right agency or consulting firm. This agency or consulting firm must look after the […]
November 16, 2022
Published by Joachim Nuyttens at November 16, 2022
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Trevalco Academy – online training

Our brand new Trevalco Academy is now live, offering online courses in validation, quality assurance and GMP compliance for the pharmaceutical industry. Trevalco Academy is our online training center through which anyone can subscribe to and follow digital, self-paced courses. We currently have 4 online trainings to offer, including two one-day trainings: We want to offer qualitative training at a reasonable price, which is possible because this is all training material we used at clients and for training of our […]
September 30, 2022
Published by Joachim Nuyttens at September 30, 2022
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Team activity: karting

Yesterday we had a fun activity with the whole Trevalco team. We first went karting, during two sessions our colleagues could show who was the fastest, most cunning driver on the track at Inkart. Afterwards we had a nice diner together at Smokt! A good time to renew connections, tell stories of summer vacations past and get updates on each other’s project activities.
September 21, 2022
Published by Joachim Nuyttens at September 21, 2022
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What’s in the new Eudralex Annex 1

A few weeks back the new and final version of Eudralex Volume 4 Annex 1 “Manufacture of Sterile Medicinal Products” was published on the website of the European Commission. This new version will come into operation on 25 August 2023, except for point 8.123 which is postponed until 25 August 2024. Where the current version of Eudralex Volume 4 Annex 1 is 16 pages, the new version has no less than 59 pages. The new EU annex 1 regulation provides […]
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