Language Learning Services and Technology
We support language & cultural training service agencies and web-based language learning tech organizations with specialist recruitment projects.
Trainers & Consultants
Clients leverage our global database of dedicated career specialists in linguistic and cultural training, both in the commercial and public sector fields.
Sales & Account Management
We work with training agencies to recruit proven sales talent to retain and build revenue streams for all types of language and cultural training projects - to enterprise and to state and local government.
Curriculum Experts
Hire experts in Learning Programs and Curriculum Development, to broaden your commercial portfolio and develop custom solutions for key clients.
Business Management
We partner with global language schools to recruit regional and international managers, overseeing daily operations, personnel and P&L objectives.
Finding the right Regulatory Affairs (RA) professional in the medical device industry can be a game-changer. These are the people who make sure your products meet all the necessary regulations, get to market smoothly, and stay compliant long after launch. But attracting the best talent starts with writing a job description that speaks their language […]
By Adaptive Life Science The European Union’s In Vitro Diagnostic Medical Devices Regulation (IVDR) — Regulation (EU) 2017/746 — represents one of the most significant regulatory overhauls in the diagnostics sector in decades. Officially applicable since 26 May 2022, the IVDR replaces the previous Directive 98/79/EC, introducing a more robust, transparent, and risk-based framework for […]
Published by Adaptive Life ScienceSpecialists in Medical Device, IVD, and Biotech Recruitment Why Internal Audits Matter in ISO 13485:2016 Internal audits are a cornerstone of any compliant Quality Management System (QMS) under ISO 13485:2016. For Quality Engineers, Regulatory Affairs professionals, and QMS leaders, these audits are not just about ticking boxes—they’re about ensuring product safety, regulatory readiness, […]
In the medical device industry, compliance with regulations is crucial to ensure the safety and efficacy of products. For companies operating in Germany and across Europe, understanding the relationship between ISO standards and the Medical Device Regulation (MDR) is essential. Understanding MDR Compliance The European Union Medical Device Regulation (EU MDR 2017/745) sets out the […]