Project Engineer

QA Resources; Cork; On-site; EUR 55,000 - 75,000; Full time

Job summary

QA Resources is seeking a Project Engineer for a leading API company in Cork on a 12-month contract. The role is fully onsite and involves supporting production process engineers, documenting technical details, and ensuring regulatory compliance.

Ideal candidates have 3–5 years in pharmaceuticals (API preferred), project engineering experience with small projects, and familiarity with cGMP environments. Visa sponsorship is not available.

Qualifications

• Experience solving manufacturing process problems.
• Strong analytical skills with quality/regulatory focus.
• Ability to work in cross-functional teams.
• Experience in pharmaceutical/cGMP environments.

Responsibilities

• Support Production Process Engineers in problem solving.
• Develop and optimize manufacturing processes.
• Prepare technical documentation.
• Ensure process compliance with quality and regulatory requirements.
• Participate in cross-functional teams and coordinate with other projects.
• Troubleshoot process or equipment issues and coordinate meetings.

Skills

Problem solving

Analytical skills

Quality assurance understanding

Cross-functional collaboration

Job description

QA Resources is currently looking for a Project 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:

• Supporting Production Process Engineers in Problem Solving and developing and optimizing manufacturing processes
• Preparing technical documentation
• Ensuring process compliance with quality and regulatory requirements
• Participate in cross-functional teams
• Troubleshooting of process or equipment issues
• Coordination of project interfaces with other projects and departments
• Coordination of project documentationCoordinate in project scheduling and project meetings

Education and Experience:

• Min 3-5 years’ experience in pharmaceuticals, preferably API manufacturing
• Project Engineering experience (small projects)
• Experience in cGMP regulated environment.
• Strong analytical skills and experience with quality assurance requirements desirable

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