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. <5% p.a.).
Required Skills
Accountability
Biopharmaceutical Industry
Biotechnology
Data Analysis
Engineering Standards
Enterprise Risk Management (ERM)
Equipment Maintenance
Leadership
Management Process
Manufacturing Process Improvements
New Product Introduction Process
People Leadership
Process Engineering
Process Improvements
Project Leadership
Quality Management Systems (QMS)
Regulatory Compliance
Regulatory Requirements
Risk Management
Safety Standards
Strategic Planning
Strategic Thinking
Team Leadership
Technology Transfer
Preferred Skills
Current Employees apply HERE
Current Contingent Workers apply HERE
Employee Status: Regular
Travel Requirements: Minimal international travel (<5% p.a.)
Requisition ID: R
Employment type: Full-time
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