• Follow-up equipment calibration plan in all RM-BG departments.
• Coordinate with concerned departments to perform process validation cleaning validation activities for all RM-BG products.
• Coordinate with concerned departments to perform qualification of steam sterilization processes and production areas/ labs qualification.
• Report outcomes of Process validation and cleaning validation activities.
• Report outcomes of Production area qualification and steam sterilization qualification activities.
• Prepare protocols
• execute and report thermal mapping activities.
• Issue new SOPs as requested.
• Record incidents
• deviations
• changes and participate in the investigation and assessment.
• Execute quality risk management projects
• health and safety risk assessment and environmental aspects & impacts.

• Experience: 0-3 Years.
• Education: Bachelor of pharmaceutical science or Bachelor of Science (chemistry section) or equivalent.
• Proficiency in English language.
• Computer literate.
• Time Management Skills.
• Communication skills.
• Analytical skills with attention to details.