Hobson Prior are currently looking for a QMS Consultant to join a fantastic pharmaceutical organisation on a contract basis located in Paris. Our client is focused on investigating a possible new class of immunotherapy with the goal to re-educate the immune system of people through the skin.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this role, you will guide the risk assessment for change control, such as risk/impact analysis, meeting, reports, etc.
• Review the design change impact on combination products with the assistance of the change control manager.
• You will redesign the quality risk management process such as procedures, templates, risk analysis format, etc.
• Evaluate QMS procedures such as CAPA, Deviation, Audit, etc, and affiliated workflow.
• Assist with the mission of the change control manager on change control assessment.
• Any other assigned duties.

Requirements:

• Familiarity within QMS SOP remediation would be ideal.
• Knowledge of design control procedures and regulatory needs suitable to combination products/medical devices.
• Know-how of ISO 13485: 2016, QSR and ISO 14971: 2019.
• Expertise on QMS major procedures such as CAPA, Deviation, Change Control, Risk Management, etc.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.