Bioprocess Engineering Manager page is loaded## Bioprocess Engineering Managerremote type: Not Applicablelocations: IRL - Meath - Dunboynetime type: Full timeposted on: Posted Todaytime left to apply: End Date: December 25, 2025 (13 days left to apply)job requisition id: R377046Job DescriptionAn amazing opportunity has arisen for a **Bioprocess Engineering Manager** to join our high preforming MS&T team in our state-of-the-art, single use multiproduct facility in Dunboyne, Co. Meath.**Key responsibilities will include**:* Oversee and mentor a team of engineers and scientists within the MS&T department, fostering a collaborative and high-performance culture.* Responsible for leading key technology transfer activities in support of clinical and commercial new product introduction projects.* Develop strategies for and support the execution of technology transfer, process, and cleaning validation programs in line with company, industry, and regulatory standards.* Function as a process Subject Matter Expert in support of process investigations and provide guidance to team members.* Utilize risk management techniques to assess strategies, prioritize activities, and initiatives.* Lead significant business-critical projects on-site associated with new product introduction and site capability build.* Support the coaching and professional development of other members of the MS&T team, ensuring continuous learning and skill enhancement.* Responsible for the use of process engineering systems and approaches for equipment design, specification and performance, generation of technical reports, process modelling, risk management, and integration of process equipment systems.* Drive the ongoing optimization of process equipment and development of future breakthrough business solutions.**Your profile**:* Minimum of a Bachelor’s Level 8 degree in a technical field (e.g., Engineering, Science, or equivalent), with experience in the biotechnology or pharmaceutical industry.* Minimum of 6 years in a biologics drug substance environment.* Technical expertise in biological drug substance upstream and/or downstream purification unit operations required.* Experience in technology transfers for clinical or commercial biologics strongly desired.* Experience with automated systems (PAS, MES) highly desired.* Process validation and cleaning validation experience desired.* Proven ability to manage multiple priorities and know when to escalate for resolution.* Flexible and self-motivated, with a proven ability to work cross-functionally to deliver technical solutions to issues.* Ability to travel internationally as the role will have a minimal travel requirement (approx.