Adjoint(e) Qualification/validation Et Analyse De Risques Procédés
Lfb Usa
Risk analysis methodology standardization
Process validation and qualification
Cross-functional coordination
You will coordinate and standardize the methodology of risk analyses related to process validation activities under the direction of the Group Industrialization Director
Job Summary
You will coordinate and standardize the methodology of risk analyses related to process validation activities under the direction of the Group Industrialization Director.
The role includes training teams on risk definition methodology, leading risk analysis documentation, and contributing to the validation/qualification strategy based on process risks.
Benefits include up to two days of telework per week after four months, transport cost coverage, additional leave days, company shuttle service, and access to company facilities such as a restaurant and gym.
Matching Summary
You will coordinate and standardize the methodology of risk analyses related to process validation activities under the direction of the Group Industrialization Director.
Skills & Requirements
Must-have
Risk analysis methodology standardization
Process validation and qualification
Cross-functional coordination
Quality by Design (ICH Q8)
Quality Risk Management (ICH Q9)
Control strategy deployment
Training on risk definition methodology
Nice-to-have
Leadership in risk analysis documentation
Transversal project management
Continuous process improvement
Cross-departmental collaboration
Expertise in equipment qualification
End-to-end product quality strategy
Key Requirements
Engineer or Bac+5 in biochemistry or related field
At least 10 years operational experience in pharma
Experience in production, quality, development, or validation/qualification