Automation Engineer

LSC, Life Science Consultants; Wicklow; On-site; EUR 57,000 - 80,000; Full time

Job summary

A biopharmaceutical company based in Wicklow is seeking an Automation Engineer to oversee automation systems and drive digital transformation projects. Candidates should have at least 5 years of experience in GMP manufacturing and proficiency in automation solutions. This role demands strong analytical and problem-solving skills. Please apply or contact us for more information.

Qualifications

• Minimum 5 years of experience in GMP manufacturing with expertise in automation.
• Understanding of pharmaceutical manufacturing processes and regulatory environments.
• Familiarity with industry standards such as GAMP, ANSI/ISA, and 21 CFR Part 11.

Responsibilities

• Oversee automation systems for maximum uptime and performance.
• Manage system user access, backups, and restores.
• Drive automation projects ensuring cost and technical goals are met.

Skills

Automation solutions proficiency

Strong problem-solving skills

Analytical skills

High communication skills

Education

Degree in engineering (automation, robotics, or computer science)

Tools

Siemens

Omron

Mitsubishi

Job description

LSC have a great contract opportunity for a Automation Engineer to join a Wicklow based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.

If you have 5+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you!

You will be a Subject Matter Expert (SME) in Manufacturing Control Systems, Operational Technology, Machine Automation, and Digitalization. You will play a crucial role in ensuring the optimal performance of our automation systems and driving digital transformation projects.

ABOUT THE PROJECT - KEY RESPONSIBILITIES:

• Oversee automation systems to ensure maximum uptime and performance.
• Manage system user access, backups, and restores.
• Implement corrective actions and collaborate with vendor technical support.
• Identify and execute small projects to enhance system performance.
• Contribute to capital planning, project execution, and documentation.
• Ensure all activities comply with site and corporate Quality Systems.
• Create and maintain engineering deliverables and test scripts.
• Develop and implement global automation strategies to standardize processes.
• Maintain and optimize automation systems and infrastructure.
• Develop solutions tailored to the manufacturing environment.
• Drive automation projects, ensuring cost, schedule, and technical goals are met.
• Stay updated with technology trends and benchmarks to keep the site at the forefront.

ABOUT YOU - ARE YOUR SKILLS A MATCH?

• Degree in engineering (automation, robotics, computer science, etc.) or equivalent.
• Minimum 5 years of work experience in GMP manufacturing, with expertise in automation. A broad understanding of pharmaceutical manufacturing processes and regulatory environments is essential. Experience in the pharmaceutical industry is advantageous.
• Proficiency in automation solutions (Siemens, Omron, Mitsubishi, etc.). Knowledge of industry standards (GAMP, ANSI/ISA, 21 CFR Part 11, Annex 11) and GxP/QA. Familiarity with ANSI/ISA-99,100 standards is a plus.
• Strong problem-solving and analytical skills, with experience in data analysis.
• Ability to work in a team-based culture, engaging with internal and external stakeholders. Collaborate with Global Automation to implement best practices.
• Contribute to the innovation roadmap and strategic planning. Mentor and train team members to enhance site expertise.
• High communication skills, an analytical mindset, and the ability to work under pressure.
• Fluent in written and spoken English.

Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!

Apply via this advert or contact Paul O'Driscoll on 021 4777 329 if you have any more questions about this opportunity!