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:
Developing and implementing process design strategies using QbD principles.
Ensuring processes are robust and consistent through CPV techniques.
Collaborating with cross-functional teams to optimize manufacturing processes.
Leading initiatives to improve product quality and efficiency.
Monitoring and analyzing data to identify areas for process improvement.
Qualifications:
Bachelor's or Master's degree in Chemical Engineering, Process Engineering, or a related field.
Proven experience in Quality by Design (QbD) and Continued Process Verification (CPV).
Strong problem-solving skills and attention to detail.
Excellent communication and teamwork abilities
- Ability to lead a project
If your skillets and experiences meet the requirements, don't hesitate, apply!
