We are currently seeking a detail-oriented Validation Engineer to join our Quality Assurance team. The successful candidate will be responsible for ensuring equipment compliance and operational excellence throughout our manufacturing processes.
Responsibilities
Design, execute, and review validation protocols to ensure compliance.
Investigate equipment failures and develop corrective actions to mitigate risks.
Foster a culture of quality and compliance within the team.
Maintain thorough documentation in accordance with company policies.
Collaborate with vendors during installation and commissioning of new equipment.
Ensure that all validation activities align with FDA and ISO standards.
Regularly audit procedures for continuous improvement.
Create validation schedules to ensure timely execution of activities.
Train and mentor junior engineers on validation practices.
Participate in industry networking to stay updated on best practices.
Requirements
Education
Bachelor's degree in Engineering or related field
Master's degree in Validation Sciences is preferred
Experience
5+ years of experience in equipment validation, preferably in pharmaceutical manufacturing.
Technical Skills
Project Management
Data Analysis
Soft Skills
Leadership
Adaptability
Languages
English: Fluent
Advantageous
Knowledge of process validation principles: Experience in applying effective validation processes.
Understanding of risk management methodologies (e.g., FMEA): Ability to identify and mitigate validation risks effectively.
Benefits
Flexible working arrangements.
Employee wellness programs.
Generous leave policies and public holidays.
Support for ongoing education and training.
Company Culture
Diversity and Inclusion: We are committed to building a diverse workforce and fostering an inclusive environment.
Employee Recognition: We celebrate our employees' achievements and contributions toward our success.
Continuous Improvement: We believe in continuous learning and improvement as a path to excellence.