Join a robust and innovative team where your expertise will significantly impact the pharmaceutical manufacturing industry. This role requires a motivated professional ready to navigate a fast-paced technical environment.

You will fit in well as a dedicated Cleaning Validation Specialist if you are detail-oriented, proactive, and keen to contribute to quality assurance processes.

• You participate in functional meetings essential for executing your responsibilities.
• You work primarily during day shifts onsite but may occasionally engage in early or late shifts as required.
• You ensure continuity in assignment execution despite absences due to various reasons.
• You perform periodic reviews of cleaning processes across three production departments to maintain validation states.
• You coordinate and execute annual re-qualification studies in alignment with operational practices.
• You provide support for cleaning projects, including method development and validation.
• You handle deviation management, including documentation and root cause analysis.