A leading biopharmaceutical company based in County Waterford is seeking a Qualification & Validation Engineer for an initial 12-month contract. The role involves ensuring processes produce products meeting quality specifications and includes authoring PPQ protocols and defining strategies for performance qualification. Candidates should have a relevant degree and experience in pharmaceutical manufacturing or quality assurance in a regulated environment. The position offers a significant opportunity to impact product quality and compliance. #J-18808-Ljbffr
We are currently looking for a Qualification & Validation Engineer – Process Performance Qualification to join a leading biopharmaceutical company based in the County Waterford area. As the Qualification & Validation Engineer – Process Performance Qualification, you will be responsible for ensuring that processes consistently produce products meeting predetermined specifications and quality attributes. This is an initial 12 month contract with possible extension. Key Duties And Responsibilities As the Qualification & Validation Engineer, you will author, review, and execute PPQ protocols and reports in alignment with global standards and regulatory expectations. As the Qualification & Validation Engineer, you will define PPQ strategy, including batch numbers, sampling plans, acceptance criteria, and statistical approaches. As the Qualification & Validation Engineer, you will contribute to the development and maintenance of the Process Validation Master Plan (PVMP). As the Qualification & Validation Engineer, you will support lifecycle management changes requiring PPQ, including technology transfers and post-approval changes. Role Requirements Relevant degree in a science or engineering discipline. Proven industry experience in pharmaceutical manufacturing, process validation, or quality assurance in a regulated GMP environment. A working knowledge and practical experience with Process Performance Qualification (PPQ) design, execution, and reporting. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. #J-18808-Ljbffr
A leading biopharmaceutical company based in the County Waterford area is seeking a Qualification & Validation Engineer – Process Performance Qualification. The role involves ensuring processes consistently meet specifications and quality attributes. Key duties include authoring PPQ protocols, defining PPQ strategies, and contributing to process validation measures. Applicants should hold a relevant degree and have experience in pharmaceutical manufacturing or quality assurance. This is an initial 12-month contract with the possibility of extension. #J-18808-Ljbffr
We are currently looking for a Qualification & Validation Engineer – Process Performance Qualification to join a leading biopharmaceutical company based in the County Waterford area. As the Qualification & Validation Engineer – Process Performance Qualification, you will be responsible for ensuring that processes consistently produce products meeting predetermined specifications and quality attributes. This is an initial 12 month contract with possible extension. KEY DUTIES AND RESPONSIBILITIES Your duties as the Qualification & Validation Engineer – Process Performance Qualification will be varied; however, the key duties and responsibilities are as follows: As the Qualification & Validation Engineer, you will author, review, and execute PPQ protocols and reports in alignment with global standards and regulatory expectations. As the Qualification & Validation Engineer, you will define PPQ strategy, including batch numbers, sampling plans, acceptance criteria, and statistical approaches. As the Qualification & Validation Engineer, you will contribute to the development and maintenance of the Process Validation Master Plan (PVMP). As the Qualification & Validation Engineer, you will support lifecycle management changes requiring PPQ, including technology transfers and post-approval changes. ROLE REQUIREMENTS To be successful in your application to this exciting role as the Qualification & Validation Engineer, we are looking to identify the following on your profile and past history: Relevant degree in a science or engineering discipline. Proven industry experience in pharmaceutical manufacturing, process validation, or quality assurance in a regulated GMP environment. A working knowledge and practical experience with Process Performance Qualification (PPQ) design, execution, and reporting. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. #J-18808-Ljbffr
