Quality Training Specialist - Ticino, Solothurn or Valais

Ticino  ‐ Vor Ort
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Schlagworte

Beschreibung

Quality Training Specialist - Ticino, Solothurn or Valais

Required Skills:

Manufacturing processing background is desired.

The resource must be proficient in the related ISO 13485 standards sections and related 21 CFR 820 regulatory subchapters

The resource should have the ability to travel and be able to work independently - with minimal supervision

Be able to work with various databases to extract and report out required information (Excel, Access, SAP etc.).

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 spread sheets and database software (Access/Excel etc. )

Fluently German or Italian and English spoken and written required.

Overall 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.

Make recommendations to achieve compliance where shortfalls are found.

Provide reports as directed.

Consultancy and guidance of all employees regarding Quality Training

Start
ab sofort
Dauer
6 months
Von
Templeton and Partners
Eingestellt
18.10.2013
Projekt-ID:
615056
Vertragsart
Freiberuflich
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