Manufacturing Engineer

Oxford Global Resources; Munster; On-site; GBP 47,000 - 64,000; Full time

Benefits offered by this job

Health insurance

Pension contributions

Paid holidays

Job summary

Oxford Global Resources is seeking an experienced Manufacturing Engineer for a global pharmaceutical leader in Kerry, Ireland. You will install, maintain and troubleshoot biologics manufacturing equipment, ensuring GMP compliance and supporting process improvements.

The role emphasizes equipment performance optimization, aseptic filling and lyophilization, with strong collaboration across teams in a regulated environment. Full-time on-site position.

Qualifications

• Experience in GMP environments in biologics/pharmaceutical manufacturing.
• Strong collaboration, communication and problem-solving skills.
• Experience with aseptic filling and lyophilization processes.

Responsibilities

• Provide daily technical equipment support and troubleshooting.
• Develop procedures and training to improve equipment operation.
• Lead technical problem solving and process improvement initiatives.
• Support validation protocol development and execution.
• Contribute to lean manufacturing and cross-functional alignment.
• Gain expertise in aseptic filling and lyophilization systems.

Skills

GMP environments

Biologics/pharmaceutical manufacturing

Collaboration

Communication

Problem-solving

Education

Bachelor's degree in Engineering or related field

Job description

Are you interested in taking the next step in your career with a global leader in the pharmaceutical industry? Are you ready to challenge yourself in a highly-regulated and fast-paced environment? Are you an experienced Engineer in GMP environments? You could be the perfect candidate for this opportunity!

Job Description

Our client are seeking an experienced Manufacturing Engineer to assume responsibility for the installation, maintenance and troubleshooting of biologics manufacturing equipment, ensuring compliance with GMP and regulatory standards while supporting process improvements and equipment performance optimization.

Key Responsibilities

• Provide daily technical equipment support and troubleshooting


• Develop procedures and training to improve equipment operation


• Lead technical problem solving and process improvement initiatives


• Support validation protocol development and execution


• Contribute to lean manufacturing and cross-functional alignment


• Gain expertise in aseptic filling and lyophilization systems.

Key Requirements

• Bachelor's degree in Engineering or related field, or equivalent experience


• Experience in biologics/pharmaceutical manufacturing and GMP environments


• Experience with aseptic filling and lyophilization processes


• Strong collaboration, communication and problem-solving skills.

Benefits

• Competitive and attractive employee compensation package


• Pension contributions


• Health insurance


• Paid holidays.

Location: Kerry Ireland