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Packaging Specialist
Job in
Riyadh, Riyadh Region, Saudi Arabia
Listed on 2026-01-29
Listing for:
Saudi Biotechnology Manufacturing Company
Full Time
position Listed on 2026-01-29
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Quality Engineering, Manufacturing Engineer, Manufacturing Production
Job Description & How to Apply Below
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 theJob Location:
Sudair Industrial City - Saudi Arabia
Working Days andHours:
Sunday to Thursday, from 8:00 AM to 5:00 PM
Position title:Finished Production Specialist
Main Responsibilities:- To carry out and supervise the packaging lines both high speed Automatic and Manual line as per the written procedures and deliver daily production output as per production plan with quality.
- To verify all the routine operational activities including machine start-ups, aid in machine adjustments, changeovers and troubleshooting.
- To provide technical assistance in the packaging processes and verify all the routine operational activities including machine start-ups, machine adjustments, changeover and troubleshooting.
- To prepare validation/qualification/Inspection protocols and execute equipment qualification like IQ,OQ and PQ etc.
- To document all the performed/verified activities, perform document compilation and review and their timely internal/external approvals.
- To write GMP documents like SOPs, CRs and perform deviation investigations and CAPA closures as per TCD
- To train the departmental staff and ensure that the personal training records are updated as per training plan.
- To ensure to prevent the machines from incidents and accidents and report immediately if observed.
- To improve the packaging process through continuous improvement, process optimization, enhancing the line output/performance with waste reduction.
- To follow GMP and SFDA guidelines, GDP, Data integrity (ALCOA principle) and safety procedures as defined in SOPs.
Experience:
Pharmacy/Engineering/Bachelor in life Sciences degree with fluency in English Language
Experience5 to 7 years in the similar function in Pharmaceutical Industry
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