We are looking for you as Validation Analyst (f/m/x) in full time (40h/week) at our Estenfeld (near Würzburg) site.

Be a part of driving clinical trials faster with your daily performance. You will be responsible for ensuring that our customers (pharma companies) can be confident that our test devices for our eCoa (digital patient diary), Respiratory (lung function devices) and Cardiac (blood pressure devices) business lines are sent out in time to arrive at medical sites (test centres and hospitals) worldwide. Make a difference by performing all operational tasks within the Warehouse, Receiving and Shipping area.

What We Offer

• Hybrid work environment (3 days in office, 2 days remote)

• Flexible working hours and working time accounts to support the work-life balance

• Support your professional development through internal and external training and certification programs

• Modern office building with an on-site canteen offering freshly cooked local dishes (with vegetarian option)

• Competitive Salary

• Company pension scheme

• The office in Estenfeld is well connected to the transport network. For public transport users, Clario offers the Deutschlandticket

• Free onsite parking

• We have both social and wellness committees that organize parties, events and activities

What You'll Be Doing

• Write concise and complete documentation to support the validation for internal clinical data systems, third party vendor systems or Patient Reported Outcome configurations. Documentation would include but is not limited to: Test Strategies, Test Reports, Test Summary Reports, Deviations and Traceability

• Evaluate new and updated systems or configurations to determine the necessary validation steps to assure compliance of those systems or configurations with industry standards and regulatory requirements

• Document and communicate deviations found during testing and maintain comprehensive tracking of all test deviations and associated corrective actions

• Interact with in-house development and operational staff in the development of system specifications and documentation

• Support Quality Assurance department with client audits by providing validation documentation, clarification of testing procedures or system demonstrations as needed

• Assist in the development of standard operating procedures related to the development, configuration, evaluation, implementation, and testing of clinical data systems or Patient Reported Outcome configurations

• Review results of test reports to ensure accurate and complete testing documentation

• Execute test reports to confirm system functionality is functioning as expected and meets the requirements of intended use

• Perform ongoing quality reviews of clinical data systems or Patient Reported Outcome configurations

• Coordinate with operational management in the identification, oversight, and training of end users in the execution of test scripts

What We Look For

• Bachelors Degree in Computer Science, Information Technology, Health/Life Sciences or Biomedical Engineering

• Minimum 1 year experience in a validation role or related job experience

• Knowledge of GCPs, 21CFR Part 11 and related electronic record requirements desired

• Excellent organizational and communication skills

• Detail oriented

• Proficiency in Microsoft Word, Microsoft Excel, and PowerPoint

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.