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Bioprocess engineering manager

Ratoath
MSD
Engineering manager
Posted: 13 December
Offer description

Join to apply for the Bioprocess Engineering Manager role at MSD
Location: Dunboyne, Co. Meath
Job Description
An amazing opportunity has arisen for a Bioprocess Engineering Manager to join our high performing MS&T team in our state‑of‑the‑art, single‑use multiproduct facility in Dunboyne, Co. Meath.
Key Responsibilities

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 escalated 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.

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