Our offer
As a QP Deputy, you will play a key role in quality assurance within our company. Your mission will be to assist the Qualified Person (QP) in various tasks and ensure the compliance of processes and products.
We offer you:
* A work environment with daily challenges
* A highly enriching variety of tasks
* The opportunity to grow within a rapidly developing pharmaceutical company
* Exposure to the world of clinical development and pharmaceutical research
Your profile
* Degree in chemical engineering, master's in science, or equivalent qualification
* Proven experience as a QP or QP Deputy
* Minimum 5 years of experience in a GMP-compliant (cGMP) environment
* Experience in aseptic production
* Excellent proficiency (C1) in French and English with strong writing skills
* Strong computer skills (MS Office, Visio)
* Commitment and autonomy in task execution
* Ability to report information effectively
* Excellent internal and external relations
* Strong team spirit
Contact
If you are ready to actively contribute and join a dynamic sector, please submit your CV via our online form along with a cover letter highlighting your relevant experience and explaining why you are interested in this position.
In case of questions, please reach out to
Your mission
* Acting as a substitute for the QP in batch confirmations/certifications under the QP's responsibility
* Approval of internal documentation
* Field presence to monitor activities and identify opportunities for improvement
* Compliance contact for external relations with clients and partners
* Participation in the management of Change Controls and continuous improvements
* Handling deviations
* Providing quality support for production, laboratory, and warehouse activities
* Drafting certificates and other documents for clients, in accordance with the company's policies