Beschreibung
On behalf of our client in the Life Science industry, Harvey Nash is looking for a Quality Training Specialist for a project until the end of the 2013 in Switzerland.
The role
Support the overall learning and development needs of the site(s) Act as lead facilitator for Global Remediation Quality Plan (GRQP) Training Process roll out Assist with deployment of all quality related training - including logistical support, data management, scheduling, in classroom assistance, and data entry as needed Implement comprehensive training program for cGMP/QSR Work with Managers and Supervisors to build learning plan requirements for all positions/employees Collaborate with Quality Training Specialist at other locations to ensure consistency Ensure training documentation is up-to-date, accurate and retrievable. Support the Quality Process Managers with the logistics of the defect awareness training. Perform a review of all training requirements once position descriptions have been updated. Demonstrate an understanding of the quality training processes and methodology in order to provide learning solutions and ensure personnel are adequately trained to perform their assigned responsibilities. Primary accountability for facilitating and implementing the qualified instructor program. Requirements
Proficient in ISO 13485 standards and 21 CFR 820 regulatory subchapters Prior experience in medical device/pharmaceutical remediation preferred Familiarity and interaction experience with regulatory auditing bodies preferred Documented training in FDA QSR, ISO required Bachelor's degree in Education, Management or related field Fluent English and German required, Italian for Ticino site Are you available immediately, have experience working within a Life Science company?
Please send your complete CV (Word documents preferred) via email. For further details feel free to call me
Im looking forward to receiving your application.
