Nos offres d'emploi

QA Specialist Pharma (M-F)



EFOR-CVO is EFOR Group’s Life Sciences brand, a result of two major consulting actors brought together at the end of 2020: Efor Healthcare and CVO-EUROPE. We have decided to join forces to assist medical device manufacturers and pharmaceutical, cosmetic and biotechnology industries, in order to become the leader in the Life Sciences consulting sector.
Our group of over 1300 experts seeks to become the market leader by providing a unique approach to consulting across the full product development cycle of our clients’ business and products and who are subjected to stringent regulatory demands.
Together with the same international aspiration, we gather unique, committed and passionate women and men, working towards our clients’ performance.
Join us now !

To support our development, we are looking for :

QA Specialist Pharma (M-F)

Permanent contract

As QA Specialist you will be responsible for quality oversight of suppliers to ensure that subsidiaries are being supplied with materials and services in compliance with the established specifications thereof.
You will perform periodic suppliers evaluation and will ensure that initial supplier qualification is being performed and continuous supplier oversight is being performed by handling of complaints, deviations and change requests.

Suppliers qualification
• Perform initial and periodic supplier qualification activities as per internal quality procedures.
• Establishment of quality assurance agreements with the suppliers.
• Involved in supplier-related aspects of new material introduction.
• Involvement in third party due diligence activities, as appropriate and required.
Suppliers Oversight
• Perform periodic supplier quality reviews.
• Manage supplier related changes as per applicable change management procedures.
• Issuance of supplier complaints and follow-up
• Handling of supplier deviations and follow-up
Quality Culture and reporting
• Drive a continuous quality and compliance improvement mindset at suppliers and third parties, such to ensure compliance with cGMP's.
• Provide adequate QA/QMS reporting on the supply operations

• Minimum of 3 years in (supply) QA in the (bio-)pharmaceutical industry
• Experience with pertinent regulations for supplier qualification (cGxP, ICH, WHO)
• Project management experience is desirable
• Strong in communication and team player
• Ability to work in fast-paced environment
• Fluent English (both written and spoken), French is an asset.
• Demonstrate day-to-day application of the company’s values.
• Ability to travel as required for business requirements, sometimes on short notice.

• An international Leader Company in the Engineering, Validation and Quality sector, which offers you interesting project.
• A strong corporate culture ensuring a personal and professional blooming and self-fulfillment.
• Overall trainings and a personal career management.
• A good salary package with lot of extra legal advantages.

Interested ? Don’t hesited to send your CV.

publication date : 29/11/2021

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