Itās our 35th anniversary, and we couldnāt be more excited. To celebrate this milestone, we wanted to take a moment to recognize how much we truly love what we do. So, we came up with a list of 35 reasons why we love working in the staffing and recruiting industry....
Life Sciences
How to Build the Right Team for IVDR Compliance
As the May 26, 2022 deadline has come and gone, now it is more critical than ever to evaluate what your organization needs to accomplish. If this feels like a daunting task, youāre not alone, as many organizations are facing the same challenges. The differences...
IVDR Compliance: The Main Challenges Ahead
In May 2017, EU officials announced regulations impacting organizations that manufacture in vitro diagnostic devices in both Europe and the United States. In order to sell their products on the European market, organizations must achieve compliance with these new...
Spotlight on: Amy Karpowicz, Senior Vice President of Local Operations
Amy Karpowicz, Senior Vice President of Local Operations, is a powerhouse who understands the value of hard work. During her 20-year tenure at Oxford, she has qualified for Presidentās Club 16 times and won multiple top awards including Recruiter of the Year, Branch...
Five Things That Keep CIOs Up At Night
In todayās business landscape, there is more pressure than ever on C-level executives. The rapid and constant technology changes occurring across industries from automotive to medical device has put the pressure on CIOs in particular. This ever-evolving landscape...
10 Signs You Need a Consulting Services Partner for Your Project
Sometimes just adding team members to your staff isnāt enough to get your project across the finish line. You need a project solution that will respond to your unique challenges, and you need help managing it. Thatās where a consulting services partner can make a...
Key Changes and Important Deadlines for MDR
In May 2017, the European Commission voted to approve new Medical Device Regulations (2017/745). This is one of the most signiļ¬cant updates of the regulations that govern medical devices in Europe in recent history. It has and will continue to involve widespread...