Beschreibung
My Client is currently looking for a Quality Training Specialist to support overall learning and development needs and to provide oversight and analysis to managers and supervisors when defining training requirements.KEY REQUIREMENTS
- EU25 Citizenship or Swiss B (Workers) Permit.
- Fluent in German (Spoken and Written).
- Manufacturing processing background is desired.
- Bachelor in Education, Management or related fields.
- Proficient in the related ISO 13485 standards sections and related 21 CFR 820.
- Documented training in FDA QSR, ISO
- Prior experience in Medical Device / Pharmaceutical remediation preferred.
- Proficient in the use of spreadsheet and database software (Access / Excel etc.)
OVERALL RESPONSIBILITIES
- Act as a facilitator for Global Remediation Quality Plan (GRQP) Training Process roll out.
- Work with Managers and Supervisors to build learning plan requirements for all positions/employees.
- Collaborate with Quality Training Specialists at other locations to ensure consistency.
- Provide leadership and execution for quality systems based training initiatives.
- Assist with deployment of all quality related training processes and methodology.
- Provide learning solutions and ensure personnel are adequately trained to perform their assigned responsibilities.
- Primary accountability for facilitating and implementing the qualified instructor program.
- Support the Quality Process Manager with the logistics of the defect awareness training.
- Perform a review of all training requirements once position descriptions have been updated.
- Implement comprehensive training program for cGMP/QSR.
- Ensure training documentation is up-to-date, accurate and retrievable.
- Make recommendations to achieve compliance where shortfalls are found.
- Consultancy and guidance of all employees regarding Quality Training.
If you are interested in this project or need further information please send your CV directly to Beni Wehrle. You can call me on
Keywords: FDA, QSR, Training, 21 CFR 820, Defect awareness, Compliance, Remediation, ISO 13485, ISO 9001, GRQP, cGMP, Medical Devices, German and English, Switzerland, Freelance
Campaign Ref: CH
To find out more about Real please visit www.realstaffing.com