Monster

Process Engineer - III - FSR Level - P3 Process Engineer - III - FSR Level - P3

eTeam UK

Brinny,, Cork

JOB DETAILS
LOCATION
Brinny,, Cork
POSTED
30+ days ago
Job Title: Process Engineer - III
Location: Brinny, Cork
Employment Type: Full-Time (Fixed Term Contract)
Duration: 03/03/2025 - 06/02/2026

Company Profile:

A global leader in innovative biopharmaceutical solutions, specializing in vaccine manufacturing, biologics processing, and advanced biotechnological production. The company focuses on state-of-the-art engineering solutions, high-quality manufacturing standards, and cutting-edge research to advance healthcare worldwide. It is committed to sustainable practices, compliance with industry regulations, and continuous improvement in process optimization.

Key Responsibilities:

•    Provide process engineering services for the design, commissioning, and qualification of a major expansion to an existing bulk vaccine processing facility.
•    Act as a client-owner representative within the Process Engineering Team to ensure successful project execution.
•    Lead cross-functional teams to deliver:
•    Equipment package design, factory acceptance testing, installation, and commissioning.
•    Product vessels, single-use mixers, single-use UFDF skids, and CIP/SIP skids.

 Job Responsibilities:

•    Support the Process Lead in implementing a Process Design based on defined project requirements.
•    Lead cross-functional teams to ensure project and site stakeholder inputs are accurately captured and reflected in commissioning and qualification (C&Q) deliverables.
•    Ensure clear communication and alignment among project stakeholders regarding key process suite activities and decisions.
•    Track and monitor progress of process suite team milestones and provide status reports.
•    Oversee C&Q execution performed by partner firms and ensure adherence to global engineering standards and best practices.
•    Coordinate and support C&Q field execution, including:
•    Development and review of system lifecycle documents (Criticality and Risk Assessments, FAT documentation, and C&Q documentation).
•    Management of installation, start-up, and testing of process systems through OQ completion.
•    Ensuring post-OQ readiness for Performance Qualification (PQ) and Process Performance Qualification (PPQ).
•    Collaborate with stakeholders, equipment vendors, and business partners to ensure seamless integration of project components.
•    Perform project engineering duties such as:
•    Preparation of schedules, work plans, and cost tracking for equipment.
•    Coordination of project activities between various stakeholders.

 Education & Experience Requirements:

•    Degree Qualification: Minimum B.Sc. or M.Sc./M.Eng in Chemical, Biochemical Engineering, or equivalent discipline. Equivalent qualifications include a Biotechnology or Industrial Chemistry degree with core chemical/biochemical engineering fundamentals.
•    Experience: Minimum of 8 years of post-academic experience in biopharmaceutical process engineering, covering design, construction, and start-up.
•    Technical & Leadership Skills:
•    Strong ability to lead and influence teams in a matrix organizational structure.
•    Excellent communication, presentation, and organizational skills.
•    In-depth understanding of process engineering and technologies relevant to bulk vaccine/biologics processing.
•    Knowledge and application of single-use technologies.
•    Familiarity with DCS/PLC process control platforms (e.g., Delta V) and industry SDLC methodologies.

About the Company

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