Engineer QC
نُشرت في :
12-12-2024
صاحب العمل نشط
1 وظيفة شاغرة
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكترونيValid email field required
أرسل الوظائف
شارك هذه الوظيفة
أرسل لي وظائف مشابهة
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكترونيValid email field required
أرسل الوظائف
الوصف الوظيفي
- 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 capabilities and collaborate with peers in Engineering, IT, QA, Manufacturing and Technology functions to provide quality oversight on assigned projects and activities.
- Support quality control work of GMP related facilities and equipment systems to ensure full compliance with GMP.
- Strictly implement job operating procedures and guidelines to complete daily experiments.
- Participate in GMP training and strictly abide by GMP and regulatory requirements
- Develop various job skills and pursue continuous improvement
- Complete other work as required by the business
- Provide quality expertise support for the project and the plant.
- Support the development of GPQS, ECMS, and GVLMS databases, providing expertise.
- Support and drive necessary departmental processes, documentation, and training.
- Support and maintain technical capabilities, and collaborate with peers in engineering, IT, QA, manufacturing, and technical functions to provide quality oversight in designated projects and activities.
- Support quality control work for GMP-related facilities and equipment systems to ensure full compliance with GMP.
- Follow job operating procedures and guidelines to complete daily experiments.
- Participate in GMP training and strictly comply with GMP and regulatory requirements.
- Develop various work skills and pursue continuous improvement.
- Requirements
- Possess a bachelor's degree and general experience in pharmaceutical quality, manufacturing, technology.
- Basic knowledge of cGMP and Global GMP requirements, quality systems, and drug/device testing techniques and pharmacopoeias.
- Possess basic knowledge of computer validation and 21 CFR 11.
- Possess good interpersonal and problem-solving skills.
- Ability to handle multidisciplinary and multi-functional work both independently and collaboratively.
- Use Chinese and English as working languages.
- Possess excellent verbal and written communication skills and the ability to communicate effectively with individuals at all levels of the organization.
- Bachelor’s degree and general experience in pharmaceutical quality, manufacturing, or technical roles.
- A basic knowledge of cGMPs and global GMP requirements, quality systems, and pharmaceutical product/device testing technology and pharmacopeia. Well -developed interpersonal and problem-solving skills.
- A basic knowledge of computer validation
- Demonstrated ability to work independently and collaboratively on multidisciplinary and multifunctional.
- Use both Chinese and English as working language.
- Excellent oral and written communication skills with the ability to communicate effectively with individuals from all levels of the organization.
نوع التوظيف
المجال
القسم / المجال المهني
المهارات المطلوبة
الإبلاغ عن هذه الوظيفة
إخلاء المسؤولية: د.جوب هو مجرد منصة تربط بين الباحثين عن عمل وأصحاب العمل. ننصح المتقدمين بإجراء بحث مستقل خاص بهم في أوراق اعتماد صاحب العمل المحتمل.
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