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Validation Process Engineer
2 weeks ago
This is an exciting opportunity for experienced professionals in GMP manufacturing settings to join our team as Validation Engineers. The successful candidate will play a crucial role in supporting several aspects of validation, including sterilization, cleaning, and controlled temperature units. Key responsibilities include designing and executing qualification/validation documentation and cycle development studies, as well as resolving technical issues encountered during study execution.
The ideal candidate will have extensive knowledge of GMP regulations and standards, as well as proficiency in Microsoft Office and job-related computer applications. Excellent communication, presentation, and interpersonal skills are essential for success in this role.
About Us
At Orion Group Life Sciences, we pride ourselves on providing high-quality recruitment services to the life sciences industry. Our company culture values fairness, respect, and inclusivity, ensuring that everyone is treated equitably regardless of their employment status.
Responsibilities
Key responsibilities of this role include:
- Designing and executing qualification/validation documentation and cycle development studies in line with the standard approval process.
- Resolving technical issues encountered during study execution.
- Engaging with production, maintenance, and quality representatives in the assigned area of operations during execution of cycle development and performance qualification activities.
