...QA, QC, C&Q, CSV, automation, and other engineering topics . Not only will you work on diversified and challenging projects, but we will also support your growth and development through a specific fol...
...QA/QC, automation, IT, and operations Drive automation and process optimization initiatives to reduce manual activities Manage project timelines, budgets, risks, and reporting Develop and refine proje...
Consultys BENELUX is looking for a Life Science Consultant to join its consulting team in VIE. As Life Science consultant, you will support our clients on diverse projects related to QA, QC, C&Q, CSV,...
...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
...ScientificCalibre Scientific is a diversified global provider of life science reagents, tools, instruments, and other consumables to the lab research, diagnostics, and biopharmaceutical communities. W...
...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
...scientific credentials to drive complex studies from initiation to completion.Key Selection Criteria:🔬 Scientific & Therapeutic Expertise:Life Sciences, Medicine, or related discipline (ideally a PhD)...
...Scientific background and knowledge of packaging and closure integrity within the pharmaceutical field. Strong understanding of European GMP, ISO13485, and 21CFR820 standards. Skilled in Microsoft Off...
...QA Engineer to reinforce its consulting team. The role of an QA Engineer is to act as the day-to-day liaison with internal and external customers for quality-related activities and ensure GMP complian...
...QA, validation, IT) and the strategic projects are in collaboration with the global QC excellence team with representatives of several other QC labs from EU/US/Canada. Competencies: Master in micro or...