Internal Operations Quality Partner

Project overview

Brabant Wallon – Contracting

For one of our clients in the biopharmaceutical sector, we are looking for a Quality Specialist to strengthen the quality activities within a biological development environment.

In this role, you will provide quality support to the manufacturing activities of biological products in the development phase. You will work in a dynamic environment where priorities can change rapidly and will collaborate closely with the production teams.

Your responsibilities

Profile sought

Assets

Our offer

Jefferson Wells offers you an indefinite-term contract (CDI) as a consultant, with an attractive salary package. You will also benefit from access to training in both technical aspects and behavioral skills (soft skills). We will support you at every stage of your career as a true professional partner.

Are you interested in this opportunity? Don't hesitate to apply!

• Location: Brabant Wallon
• Type: Contracting
• Job #28155
• Participate in daily interactions and meetings with production teams.
• Ensure real-time monitoring of manufacturing activities and batches.
• Perform batch record review.
• Manage deviations and contribute to the follow-up of associated actions.
• Work on quality systems such as: Deviations, Change Control, CAPA
• Conduct on-site GMP checks, compliance tours, and mini-audits when necessary.
• Collaborate with various stakeholders to resolve quality issues.
• Write, update, and manage quality documentation, including: SOPs, Protocols, Reports
• Ensure a balance between operational presence on the ground and documentation activities.
• Bachelor's or Master's degree with a scientific orientation.
• Experience in a GMP environment.
• Knowledge of quality systems (deviations, CAPA, Change Control).
• Ability to manage multiple priorities simultaneously.
• Good organization and prioritization skills.
• Ability to work in a constantly evolving environment.
• Good interpersonal skills and team spirit.
• Proactive, autonomous, and solutions-oriented approach.
• Willingness to combine field work and administrative tasks.
• English level sufficient to participate in professional meetings.
• Experience in the pharmaceutical or biological products industry.
• Production experience.
• Good knowledge of regulatory requirements.
• Ease in stakeholder management.
• Interest in continuous improvement and on-the-job learning.

Project details

• Start: flexible
• Location: Brabant Wallon, BE
• Languages: French