Job Title: Senior Process Engineer
Location: Limerick, Ireland
Employment Type: Technical / Engineering
About the Role
We are seeking an experienced Senior Process Engineer to join a high-performing process engineering team in Limerick.
In this role, you will support manufacturing operations within a designated product value stream, driving process excellence, troubleshooting technical issues, and supporting product transfers across sites.
You'll have the opportunity to directly influence product quality, operational efficiency, and innovation within a regulated environment.
Key Responsibilities
Provide technical leadership within a manufacturing value stream.
Drive continuous improvement initiatives focused on product quality, yield, and overall equipment effectiveness.
Lead or support corrective and preventive actions (CAPA) for manufacturing and process quality issues.
Utilize strong analytical thinking and data-driven decision-making to solve complex process problems.
Collaborate cross-functionally with engineering, operations, quality, and other stakeholder groups.
Manage and coordinate multiple engineering projects, including change management through quality systems.
Apply statistical methods and troubleshooting techniques to ensure process control and stability.
Conduct process validation activities for products on both existing and new production lines.
Stay current on emerging process technologies, leveraging innovative solutions to enhance performance.
Communicate technical findings clearly and effectively across the organization.
Education & Experience Requirements
Essential
Honours Level 8 degree (B.Sc./B.Eng.) in Physics, Chemistry, Biological Science, or Mechanical/Material/Process Engineering.
Minimum 7 years' engineering experience within a GMP manufacturing environment.
Proven track record of delivering results in a technical or manufacturing setting.
Desirable
Strong project management capability (FPx or equivalent).
Excellent interpersonal and communication skills.
Skilled in problem-solving methodologies and capable of managing multiple initiatives concurrently.
Highly self-motivated with strong ability to influence in cross-functional teams.
Competent in MS Office Suite.
Experience with advanced statistical tools and methodologies (DOE, capability analysis, hypothesis testing, Six Sigma/Black Belt concepts).
Familiarity with process validation in a regulated medical device or pharmaceutical manufacturing environment.
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