Process Engineer

QA Resources Ltd; Cork; Hybrid; EUR 55,000 - 75,000; Full time

Job summary

QA Resources Ltd in Cork is seeking a Process Engineer for a leading API company on a 12-month, fully onsite contract. You will lead the delivery of engineering projects, oversee commissioning and qualification activities, and drive cross-functional collaboration to meet project goals.

Ideal candidates will have 3+ years of pharmaceutical API experience, a third-level degree, and a background in cGMP environments. Project experience is a plus; visa sponsorship is not available.

Qualifications

• Third level degree.
• Min 3 years experience in pharmaceuticals, preferably API manufacturing.
• Ideally project experience (new and/or brown sites).
• Experience in cGMP regulated environment.

Responsibilities

• Lead the delivery of Engineering projects on time, on budget & in accordance with all project & business goals.
• Oversee and support commissioning and qualification activities
• Participate in and lead Cross-Functional teams as necessary.
• Updating & influencing management and project stakeholders.
• Troubleshooting of process or equipment issues
• Coordination of project interfaces with other projects and departments
• Provide process and equipment related training as required.
• Completion of assigned tasks to support manufacture of quality medicines in accordance with cGMP and EHS requirements.

Education

Third level degree

Min 3 years experience in pharmaceuticals, preferably API manufacturing

Ideally project experience (new and/or brown sites)

Experience in cGMP regulated environment

Job description

Description

QA Resources is currently looking for a Process Engineer on behalf of a leading API company based in Cork. This is an initial 12-month contract role. This is a fully onsite position.

Overview

• Lead the delivery of Engineering projects on time, on budget & in accordance with all project & business goals.
• Oversee and support commissioning and qualification activities
• Participate in and lead Cross-Functional teams as necessary.
• Updating & influencing management and project stakeholders.
• Troubleshooting of process or equipment issues
• Coordination of project interfaces with other projects and departments
• Provide process and equipment related training as required.
• Completion of assigned tasks to support manufacture of quality medicines in accordance with cGMP and EHS requirements.

Education and Experience

• Third level degree
• Min 3 years experience in pharmaceuticals, preferably API manufacturing
• Ideally project experience (new and/or brown sites)
• Experience in cGMP regulated environment.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***