Quality Training Specialist Job in Switzerland

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Quality Training Specialist Job Description

Pauwels Consulting is currently looking for a Quality Training Specialist to support the overall learning and development needs of the site(s) for our pharmaceutical partner in Switzerland.


The main responsibilities of the Quality Training Specialist are:
 

• Support the overall learning and development needs of the site(s)
• Provide oversight and analysis to managers and supervisors when defining training requirements.
• Act as lead 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 Specialist at other locations to ensure consistency
• Provide leadership and execution for quality systems based training initiatives
• Assist with deployment of all quality related training – including logistical support, data management, scheduling, in classroom assistance, and data entry as needed
• 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
• 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
• 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
• Provide reports as directed
• Consultancy and guidance of all employees regarding Quality Training

Quality Training Specialist Job Requirements

What does Pauwels Consulting require from the Quality Training Specialist:
 

• Bachelor’s degree in Education, Management or related field
• Quality / compliance experience in the medical device, pharmaceutical industries or similarly regulated industry
• Documented training in FDA QSR, ISO 13485 / 9001 required
• Familiarity and interaction experience with regulatory auditing bodies preferred
• Prior experience in medical device / pharmaceutical remediation preferred
• Proficient in the use of spreadsheet and database software (Access / Excel etc.)
• Analytical, thorough, accurate and proficient in the use of computers
• Manufacturing processing background is desired
• Proficient in the related ISO 13485 standards sections and related 21 CFR 820 regulatory subchapters
• Be able to travel and be able to work independently – with minimal supervision
• Excellent organizational skills, readiness to take on responsibility, reliable, proactive & self-driven, customer oriented
• Be able to manage effectively multiple priorities and tasks
• Excellent communication skills with all levels for employees
• Know and follow the guidelines regarding the code of conduct, ethics and compliance programs and other relevant regulations at all times.
• Team player
• Fluently German / English spoken and written required
• For the Italian speaking site, knowledge of Italian is mandatory

Quality Training Specialist Application Information

What can you expect from Pauwels Consulting.

A responsible position in a leading international company.
Personal development opportunity’s through learning on the job and additional external trainings.
You can expect a market oriented compensation, including a wide range of fringe benefits


Please apply with your CV and cover letter by the 'apply' button below

Quality Training Specialist Summary

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