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

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.

Division: eTeam Workforce Limited-Ireland Reference: 25-03694