Job Opportunity
We are seeking a skilled Validation Engineer to coordinate the development and maintenance of our site validation program, ensuring compliance with regulatory, quality, and industry standards.
The ideal candidate will have at least 3 years of experience in validation, preferably in medical device plastics processing or assembly operations, and a strong understanding of cGMP and regulatory requirements.
Main Responsibilities:
* Coordination and participation in the validation and qualification of site equipment, utilities, processes, and software.
* Generation of validation and qualification protocols and final reports to cGMP standards.
* Generation of validation investigations and implementation of corrective actions.
Skills and Qualifications:
* Strong communication (written and oral), presentation, and troubleshooting skills required.
* Effective interpersonal and organizational skills.
* Ability to work well both independently and in a team environment.
* Capable of prioritizing work and multitasking.
About This Role
This is an exciting opportunity for individuals looking to contribute to a dynamic team and advance their career in validation engineering. If you are passionate about delivering high-quality results and committed to excellence, we encourage you to apply.