Recruitment of Project Managers has been a core specialty of Adaptive Globalization for over a decade.
We understand that it isn’t enough for a candidate to have held a ‘PM’ title within the industry to automatically qualify for a job. Our in-depth screening process matches key experience with specific vacancies.
Technology Expertise
Need a PM with strong skills in Trados, MemoQ, InDesign, or Smartling? We’ll make it a must-have in our search.
Different LSPs require different levels of hands-on tech knowledge from their PMs, so we prioritize accordingly.
Language Skills
For PMs assigned to specific global accounts, communication is crucial.
Adaptive can help to find candidates with the right PM background plus the native language skills to support customers, work with suppliers and approve linguistic quality.
Client-Facing Experience
If your agency’s PM vacancy involves regular interaction with key clients and contributes to sales and growth, we’ll focus our search on customer service experience, communication skills and personality.
Project Scope
‘Managing projects’ means nothing without context. Document translation or web localization?
Three languages or 30? Word counts, budgets and time-frames also play a major role.
We look to find the PM candidate whose experience truly fits with your company’s needs.
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 […]