Our client is a leader in the pharmaceutical industry. We are currently looking for a Senior Process Engineer to implement pharmaceutical manufacturing processes following Quality by Design (QbD) principles and Continued Process Verification (CPV), on a temporary contract.
In this role, you will be responsible for:
1. Developing and implementing process design strategies using QbD principles.
2. Ensuring processes are robust and consistent through CPV techniques.
3. Collaborating with cross-functional teams to optimize manufacturing processes.
4. Leading initiatives to improve product quality and efficiency.
5. Monitoring and analyzing data to identify areas for process improvement.
Qualifications:
1. Bachelor's or Master's degree in Chemical Engineering, Process Engineering, or a related field.
2. Proven experience in Quality by Design (QbD) and Continued Process Verification (CPV).
3. Strong problem-solving skills and attention to detail.
4. Excellent communication and teamwork abilities.
5. Ability to lead a project.
If your skills and experiences meet the requirements, don't hesitate, apply!
#J-18808-Ljbffr