Davipharm

Job description

• Organizing, taking part in, and providing process supervision over transfers and implementations of new technologies
• Drafting transfer and process documentation, and ensuring its consistency with the documentation constituting the base for a medicinal product to obtain marketing authorization
• Taking part in proceedings concerning inconsistencies in the process of manufacturing medicinal products
• Improving the quality and efficiency of processes by implementing continuous development tools
• Providing training and supervision over the implementation and application of technology to the production process
• Working together with all the departments involved in the transfer to ensure seamless execution
• Taking part in internal audits, contractor audits and inspections

Job requirement

• Bachelor’s degree in engineering, pharmacist or related field of study.
• 1 year of work in pharmaceutical production or pharmaceutical development preferred.
• Experience in manufacturing Solid; Topical and Oral Liquide Dosage Form.
• Knowledge of basic production equipment: principles of operation, maintenance and safety.
• Knowledge of problem-solving methods (5 whys, Fishbone, PDCA, …)
• Understand the systematic process of WHO-GMP or equivalent EU-GMP, PIC/S in the pharmaceutical industry.
• Good skills in MS Office: Microsoft Excel, Word, Power Point,
• Good command of English
• Cooperation with R&D Department; QA/QC, Validation, Production, Engineering, Supply Chain Department in accordance with internal rules.

Please contact our Recruiter or apply via email recruitment@davipharm.info