Validation Engineer

Ellab; Dublin; On-site; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Competitive salary

Career growth

Collaborative environment

Job summary

Ellab Ireland is seeking a skilled Validation Engineer to ensure compliance and efficiency in validation processes for our Dublin project. You will contribute to development and implementation of validation strategies across multiple systems, collaborating with cross-functional teams.

The role emphasizes SIP system validation, regulatory alignment, and continuous improvement, offering a dynamic, collaborative environment and opportunities for career growth.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or related field.
• Proven experience in validation engineering, particularly with SIP systems.
• Strong understanding of validation methodologies and regulatory requirements.

Responsibilities

• Develop and execute validation protocols for systems and processes.
• Collaborate with cross-functional teams to identify validation requirements.
• Ensure compliance with regulatory standards and internal policies.
• Conduct risk assessments and make recommendations for improvements.
• Troubleshoot validation issues and implement effective solutions.

Skills

Validation engineering

SIP systems

Regulatory compliance

Problem-solving

Communication

Education

Bachelor’s degree in Engineering, Life Sciences, or related field

Job description

Ellab Ireland provide leading validation, monitoring and calibration solutions and services across all major pharmaceutical sites. We are currently recruiting for Validation Specialists and Engineers, with all levels of experience, from science and engineering backgrounds for our Dublin based project.

Role Overview:

We are seeking a skilled Validation Engineer to ensure compliance and efficiency in our validation processes. You will play a key role in the development and implementation of validation strategies across various systems.

Key Responsibilities:

• Develop and execute validation protocols for systems and processes.
• Collaborate with cross-functional teams to identify validation requirements.
• Ensure compliance with regulatory standards and internal policies.
• Conduct risk assessments and make recommendations for improvements.
• Troubleshoot validation issues and implement effective solutions.

Qualifications:

• Bachelor’s degree in Engineering, Life Sciences, or related field.
• Proven experience in validation engineering, particularly with SIP (Sterilization In Place) systems.
• Strong understanding of validation methodologies and regulatory requirements.
• Excellent problem-solving skills and attention to detail.
• Effective communication and collaboration skills.

What We Offer:

• Competitive salary and benefits.
• Opportunities for career growth and professional development.
• A collaborative and innovative work environment.