وظائف في Gmp في عمّان

Responsibilities Provide quality expertise support to projects and factories. Assisted in the development of GPQS, ECMS, GVLMS databases and provided expertise. Support and drive necessary departmental processes, documentation and training. Support and maintain technical capa المزيد...

Job Description Is the responsible party for overseeing the design, implementation and delivery of a common Quality system and strategy for GMP and GDP activities across in Commercial marketing company for all of the AZ product portfolio in Malaysia. Participates in developme المزيد...

Responsibilities Oversee the entire manufacturing process, from upstream to downstream operations, ensuring that all processes are carried out in accordance with established protocols and regulations. Manage the production of biopharmaceutical products, ensuring that they meet المزيد...

المسؤوليات . تشغيل ومراقبة معدات إنتاج الأدوية وفقًا للإجراءات والبروتوكولات المعمول بها. . إجراء عمليات إعداد المعدات وتنظيفها وتغييراتها وفقًا لمعايير GMP (ممارسات التصنيع الجيدة). . تنفيذ دفعات الإنتاج ووزن المواد الخام وقياسها بدقة وتوثيقها. جميع أنشطة التصنيع. . اتبع إرشادات الس المزيد...

bout the job ■ Job Description General quality assurance work related to GMP/GQP① Maintenance and management of quality management systems that comply with domestic and global requirements ② Building and standardizing robust processes through collaboration with manufacturing المزيد...

اتبع لوائح توجيهات GMP وGLP وقواعد إجراءات التشغيل القياسية الداخلية. القيام بجميع أنشطة التحليل الكيميائي والفيزيائي. تحليل وتطوير والتحقق من صحة الأساليب التحليلية. الممارسة في استكشاف الأخطاء وإصلاحها التحليلية مع الأخذ في الاعتبار قسم إجراءات التشغيل الموحدة وقواعد GLP. خطط تحليل المزيد...

Participate in different stages of the project and provide valuable and professional suggestions to the project construction as an end user Fully involved in different project phase and have valuable input as end user Learn and apply best practices from other plants and in المزيد...

Accountabilities: As a QC Microbiology Analyst, you will be responsible for implementing methods and techniques for analysis of cell therapy products, such as: bioburden, endotoxin, gram staining, and sterility. You will handle routine QC lab tasks such as technical transfer test المزيد...

Accountabilities: As a Senior Process Facilitator, you will provide direction to PET personnel, promote safe work practices, ensure cGMP’s are used and followed during production, and promote a positive work environment. You will also be responsible for training of PET pe المزيد...

About the job Job Responsibilities WH operation (Supply and Cost): External goods receipt according to AZ GMPs. External goods delivery to customers. Good cleaning & maintaining practices during all warehousing activities. Internal goods delivery to relevant te المزيد...

Responsibilities: Excellent employment opportunity for a Senior QCISO Analyst in the Frederick, MD area. (100% onsite) Typical day will include project work, password resets, user access requests, software troubling shooting, make restricted folders for users, writing SOPs, ex المزيد...

About the job Working with site local team to create the Front-End Study “FES” for the Expansion Project. Work with Global Engineering and Global Engineering Procurement to RFP, chose & award third parties “Engineering Consultant” Work closely with المزيد...