Production 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.

About the Job Location:

Sudair Industrial City - Saudi Arabia

Working Days and Hours:

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

Position title:

Main Responsibilities

• Support the planning, coordination, and execution of Technology Transfer and New Product Introduction activities.
• Maintain project trackers, action logs, timelines, risks, dependencies, and readiness status for assigned products.
• Coordinate activities between the sending unit, Manufacturing, QA, QC, Validation, Engineering, Supply Chain, Regulatory Affairs, and external partners.
• Review Technology Transfer documentation, perform gap assessments, and follow up on identified actions until closure.
• Support the transfer of manufacturing, assembly, inspection, packaging, and analytical testing processes to the receiving site.
• Support Change Controls, risk assessments, deviations, CAPAs, qualification, process validation, and analytical method transfer activities.
• Participate in engineering, qualification, validation, and commercial batch execution, including shop-floor technical support.
• Ensure all Technology Transfer activities are completed in compliance with cGMP, company procedures, quality requirements, and approved timelines.
• Support technical training, knowledge transfer, lessons learned, and continuous improvement activities.

Qualifications and Experience

Educational Qualification

Bachelor’s degree in Pharmaceutical Sciences, Pharmacy, Biochemical Engineering, Biotechnology, Biology, or another relevant scientific discipline.

Work Experience

• Minimum 2–5 years of relevant experience in the pharmaceutical, biopharmaceutical, biotechnology, medical-device, or regulated manufacturing industry.
• Practical knowledge of cGMP manufacturing and pharmaceutical quality systems.
• Experience working with multidisciplinary teams and tracking technical activities to completion.
• Experience preparing or reviewing controlled technical documentation.
• Experience supporting shop-floor manufacturing, qualification, validation, or batch-execution activities.
• Professional working proficiency in English, both written and spoken.