Process Validation Engineer - Pharmaceutical Industry (M/F)

Joining Meent means?

Joining an engineering company expert in Life Science, created in 2023, which values the talent and energy of its employees to carry out innovative and ambitious projects.

At Meent Life Science, we build an adventure with our employees based on:

• Mutual aid and team spirit
• Benevolence and stability
• Fulfillment and professional progression

We believe that a fulfilled employee is a high-performing employee. That is why we offer a stimulating environment, training opportunities, and long-term support in your career.

The position:

• Define and deploy the validation strategy for pharmaceutical manufacturing processes.
• Write and update process validation protocols and reports.
• Participate in the definition of critical process parameters and critical quality attributes.
• Lead and monitor validation trials in collaboration with the Production, Quality, MSAT, and Industrialization teams.
• Analyze data from validation batches and rule on process compliance.
• Participate in investigations related to deviations, CAPA, and changes impacting manufacturing processes.
• Contribute to maintaining the validated state and monitoring process performance.
• Ensure compliance of activities with GMP / BPF requirements and site quality procedures.
• Participate in the continuous improvement of processes and validation practices.

Profile sought:

• You hold a degree from an engineering school, a scientific master's degree, or equivalent training.
• You have 3 to 5 years of experience in manufacturing process validation in the pharmaceutical industry.
• You master process validation principles and GMP / BPF requirements.
• You have a good understanding of pharmaceutical manufacturing processes and the challenges associated with their control.
• You are comfortable with data analysis, documentary writing, and quality deviation management.
• Experience in equipment qualification, industrial transfer, or cleaning validation would be a plus.
• You are rigorous, autonomous, structured, and comfortable in a cross-functional environment.
• You have a good level of professional English.