Caring for the world ... one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.
Coordinate workflow and DePuy Synthes priorities of Document Control activities.
Collaborate with Change Owners to efficiently analyze, manage and conduct COs.
Conduct impact analyses of COs, assess change readiness and identify key requirements.
Communicate CO status information as requested.
Proactively seek methods of increasing efficiency while maintaining compliance in all areas of responsibility on a continuing basis.
Provide historical and current documentation in response to queries from management and other departments as needed.
Exhibit excellent organizational and communication skills.
Properly employ all SOPs, Work Instructions, Training Guides and Forms in the performance of tasks within the organization.
Maintain a work environment that provides open communication and personnel growth.
Be an extremely flexible team player adaptable to change.
Perform other special projects and support functions as assigned by the Supervisor.
Required to know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.
Diligently participate in our compliance program-related activities as denoted by the Supervisor or our Chief Compliance Officer.
Who we are looking for
Proficient with Microsoft Office products (Word, Excel, Power Point, etc.) is required.
Familiarity with Documentation Control PC-Based tools is prefered.
Familiarity with GMP and/or ISO regulated environment is preferred.
Fluent in French is required, proficiency in English is preferred.
Medical device, Pharmaceutical and/or Biotech experience is preferred.
This role based in Le Locle (NE), Switzerland will initially be limited to approx. 3-6 months. If you are interested in working for a global leading health care company in a challenging role, then send us your application in English today. Or give us a call if you have any questions!