About the job
We are on the lookout for a dedicated and enthusiastic Validation Engineer to contribute to our validation efforts in regulated sectors such as Pharmaceuticals, Biotechnology, Medical Devices, Chemicals, and Food Manufacturing. The Validation Engineer's primary role will be to ensure that our equipment, systems, and processes comply with regulatory standards, thereby safeguarding product quality and patient safety.
Key Responsibilities:
- Design, develop, and implement validation protocols (IQ, OQ, PQ) for machinery, utilities, facilities, and production systems.
- Facilitate the validation of laboratory instruments, manufacturing equipment, cleaning procedures, and computerized systems.
- Ensure adherence to cGMP, FDA, EMA, and other relevant regulatory guidelines.
- Prepare and evaluate validation documentation, including protocols, reports, SOPs, and risk assessments.
- Conduct troubleshooting and root cause analysis for any validation or equipment-related discrepancies.
- Collaborate with multidisciplinary teams (Engineering, Quality, Manufacturing, Laboratory) to achieve project goals.
- Engage in change control, CAPA, and continuous improvement projects.
- Maintain precise records and ensure that documentation remains audit-ready at all times.

