SAP Quality Assurance Validation Consultant (M/F)

MEENT is a leading company in the life sciences field, offering solid expertise in engineering consulting and clinical research. Our commitment to innovation and quality allows us to provide tailored solutions in response to the complex challenges of our clients in the Healthcare sector.

The position:

MEENT is looking for its future Quality Assurance and SAP Validation talent in Occitanie!

As part of the evolution of its industrial information system, an international pharmaceutical laboratory is continuing the deployment of its SAP platform across several production sites. This transformation aims to harmonize Quality processes, strengthen regulatory compliance, and improve the operational performance of teams.

To support this dynamic, the laboratory is looking for a SAP Quality Consultant capable of acting as a key interlocutor between business teams, project teams, and international stakeholders. The consultant will contribute to securing Quality processes, supporting users, and ensuring the success of the various phases of the program.

The consultant will work on the following activities:

Support for the transformation of Quality processes

• Analyze existing Quality processes and propose areas for improvement in SAP.
• Participate in functional workshops with business teams.
• Contribute to the definition of needs and their translation into operational solutions.
• Ensure the harmonization of practices between different industrial sites.

Qualification and validation of solutions

• Participate in the validation strategy for deployed functionalities.
• Prepare, coordinate, and execute functional and user testing campaigns.
• Ensure the follow-up of anomalies until their resolution.
• Contribute to the drafting of validation deliverables in accordance with GxP requirements.

User support and change management

• Prepare communication and training materials.
• Lead training sessions for key users.
• Support teams during the production rollout and hypercare phases.
• Facilitate the adoption of new processes and collect field feedback.

Documentary governance

• Update procedures, work instructions, and Quality documents.
• Guarantee documentary consistency between the different sites concerned.
• Ensure compliance with documentary standards and regulatory requirements.

Activity management

• Ensure the follow-up of assigned actions and produce regular reporting.
• Participate in project meetings and contribute to indicator monitoring.
• Identify risks related to deployment and propose appropriate mitigation actions.
• Participate in the continuous improvement of processes and working methods.

Profile sought:

Proven experience in the pharmaceutical or life sciences industry; Good mastery of Quality Assurance processes in a GxP regulated environment; Participation in one or more SAP or ERP projects in an industrial context; Ability to operate in an international and multicultural environment; Professional English, both written and spoken.