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 (Qb D) 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 Qb D 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 (Qb D) 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 skills and experiences meet the requirements, don't hesitate, apply!
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