Visual Inspection Specialist

Saudi Biotechnology Manufacturing Company (SAUDIBIO) is a Saudi Joint Stock Company and was established in 2010. A leading biopharmaceutical company duly incorporated in the Kingdom of Saudi Arabia, Saudi Bio has a multipurpose sterile fill and finish facility for biopharmaceutical products and is a leading insulin manufacturer in Saudi Arabia.

Location:

Sudair Industrial City, Riyadh Region, Saudi Arabia

Working Days and

Hours:

Sunday to Thursday, from 8:00 AM to 5:00 PM

• Responsible to validate and establish the visual inspection process as a Subject Matter Expert (SME) that includes test kit preparation and other related activities and tasks
• Coordinating the collective efforts of other departments or outside contractors / Vendors to complete visual inspection operation project tasks
• Provides technical support in the process technology, implementation and scale-up, and to support feasibility studies with external stakeholders
• Developing interpersonal capabilities in the areas of aseptic production and providing training, support, and guidance to all team members of aseptic production
• Responsible for visual inspection process validation and qualification activities by means of end-to-end validations such as from Change control, URS to PPQ
• Responsible for complete commissioning & qualification activities of visual inspection as per the regulatory needs and strive to reduce expenses and increase productivity
• Authoring and reviewing GMP documents of aseptic production department, such as qualification and validation protocols, summary reports and associated data for conformance to regulations and SOPs, but not limited to
• Working with aseptic production team effectively to achieve the strategic goals and objectives of the organization
• Proactively support the quality management system elements of aseptic production departments such as deviation notifications, investigations, CAPA, change management and risk assessments

• Educational
  
  Qualification:
  
  Bachelor of Pharmacy/Engineering
• Work Experience:
  
  7 to 12 years

Mid-Senior level

Full-time

Production

Biotechnology Research and Pharmaceutical Manufacturing