Beschreibung
Projekt Nr.: A3945Funktion Training Specialist (contract)
Branche Medizintechnikunternehmen
Pensum 100%
Arbeitsort Bern Ost, Tessin und Deutschland
Antrittstermin asap
Dauer 6 Monate mit Option
Anzahl Stellen 7
Stellenbeschreibung
https://www.ghrgroup.ch/projekt-details/orderNr/A3945.html
Für unseren Kunden suchen wir mehrere sehr erfahrenen Training Specialist wie folgt:
Main Responsibilities:
- 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.
Desired competencies:
Analytical, thorough, accurate and proficient in the use of computers.
ISO 13485 standards sections and related 21 CFR 820 regulatory subchapters.
the ability to travel and be able to work independently – with minimal supervision
Bachelor’s degree in Education, Management or related field.
Be able to work with various databases to extract and report out required information (Excel, Access, SAP etc.).
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.
Quality / compliance experience in the medical device, pharmaceutical industries or similarly regulated industry.
Documented training in FDA QSR, ISO 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. )
Unique Selling Points: FDA QSR, ISO 13485
Manufacturing processing background
Diverse Tätigkeiten gemäss Projektleiter
Anforderungen
IT Profil Priorität
Teacher ein Muss
Trainer ein Muss
Sprachen
Sprache mündlich schriftlich Priorität
Deutsch sehr gut sehr gut ein Muss
Englisch gut gut ein Muss
Italienisch gut gut ein Muss
Wir freuen uns auf Ihre Bewerbung
André van Sprundel
CEO
GHR Global Human Resources AG
Blegistrasse 13
CH-6340 Baar / ZG
Tel:
Direktnr:
Fax:
E-Mail:
Web: www.ghrgroup.ch
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