ICON

Validation Analyst II, Labs

In short

Validation Analyst II, Labs at ICON, a global healthcare intelligence and clinical research organisation, ensures the accuracy, reliability, and compliance of laboratory processes and systems supporting clinical trials. The role covers developing and executing validation protocols for lab instruments and software, validation testing, data analysis, documentation, and troubleshooting deviations, plus guidance to project teams on validation strategies. It requires a Bachelor's degree in Life Sciences, Engineering, Computer Science, or related field, at least 2 years of laboratory validation or quality assurance experience in pharma, biotech, or clinical research, knowledge of FDA/EMA/ICH regulatory requirements, and willingness to travel about 5%.

About the Role
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Validation Analyst II, Labs at ICON, you will ensure the accuracy, reliability, and compliance of laboratory processes and systems supporting clinical trials.
What You Will Do
You will take responsibility for quality assurance and compliance deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
•Collaborating with laboratory and quality assurance teams to develop and execute validation protocols and test plans for laboratory instruments, equipment, and software systems.
•Conducting validation testing, data analysis, and documentation in accordance with regulatory requirements and industry standards.
•Identifying and troubleshooting validation issues, deviations, and non-conformances, and implementing corrective and preventive actions as needed.
•Providing technical expertise and guidance on validation strategies, best practices, and regulatory expectations to project teams and stakeholders.
•Contributing to the continuous improvement of laboratory processes, systems, and validation methodologies.
Your Profile
You will bring relevant quality assurance and compliance experience, along with the following qualifications and skills.
Required qualifications and experience:
•Bachelor's degree in Life Sciences, Engineering, Computer Science, or related field.
•Minimum of 2 years of experience in laboratory validation, quality assurance, or related role within the pharmaceutical, biotechnology, or clinical research industry.
•Strong understanding of regulatory requirements (e.g., FDA, EMA, ICH) governing laboratory operations and validation activities.
•Proficiency in validation methodologies, documentation practices, and quality management systems.
•Excellent analytical, problem-solving, and communication skills, with the ability to work effectively in a cross-functional team environment.
•Willingness to travel as required (approximately 5%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
•Competitive base salary and performance related incentives
•Health and wellbeing programmes including medical, dental, and vision coverage where applicable
•Retirement and pension plans
•Life assurance and disability coverage
•Employee assistance programmes and wellbeing resources
•Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.

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