On behalf of our client, we are looking for a
QS Analyst (Training & Document Control).
Contract
: Temporary unlimited
Location
: Le Locle
Home office:
max 1 day per week
Availability
: ASAP or with
maximum 1-month notice
Languages
: French and English fluency required
Responsibilities:
* Manages and Maintains the Training Curriculum Process
* Coordinates classroom training sessions
* Participates to New Hire Orientation Process
* Participate to project for training program improvement (CAPA)
* Change order management : review document, add approvers, add tasks, launch for training, coordinate process till implementation
Requirements:
* Minimum of 1-2 years' experience in document and promotional materials management using electronic document management systems (Agile or Adaptiv or other PLM system)
* Minimum of 1-2 years' experience in a Quality Systems / Regulatory Compliance environment with a working knowledge preferably in the medical device or pharmaceutical industries
* Minimum of 1-2 years' experience in a Learning Management System (LMS) and its use to deploy training programs and requirements across the company
* Knowledge or experience working in an FDA and/or European regulatory environment
* Thorough understanding of GMP (Good Manufacturing Practices)/ISO (International Organization for Standardization) regulations
* Written and verbal effective communication skills in English and in French including presentations as assigned
* Proficient in Microsoft Office tools - Word, Excel, and PowerPoint
* Solid document management skills
* Strong communication, organizational, negotiation and interpersonal skills
* Autonomous / Conscientious / Rigorous / Analytical Mind / Flexible
* Well organized and systematic approach
* The ability to collaborate with all levels of management across multiple sites and functions