Job description:
- Develop and execute commissioning and qualification protocols.
- Prepare and maintain detailed validation documentation.
- Ensure compliance with GMP, GLP, and other relevant standards.
- Troubleshoot and resolve system performance and compliance issues.
- Support continuous improvement and stay updated on industry best practices.
Requirements:
- Education: Bachelor’s degree in Engineering, Life Sciences, or related field
- Experience: Experience in commissioning, qualification, or validation within a regulated industry.
- Skills: Knowledge of C&Q principles, regulatory requirements, strong problem-solving abilities, and excellent communication skills.
- Regulatory Knowledge: Familiarity with FDA, EMA, and other relevant regulations.
