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Link:Lian Chuang Biomedicine
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Workshop director
Job Responsibilities:

1. Carry out the company's various management systems to ensure that the company's goals and tasks are completed; responsible for the overall dispatch management and normal safety of the workshop; report the safety, environmental protection and occupational health issues of the workshop;
2. Respond to the abnormal situation in a timely manner, find problems in a timely manner, and make reasonable suggestions;
3, responsible for the correct use of the process equipment owned and maintained according to equipment maintenance and maintenance procedures to make it in good condition;
4. Responsible for organizing the training and assessment of the employees of this workshop, rationalizing the human resources of the workshop, and reporting to the company for approval;

job requirements:
1, with chemical synthesis, pharmacy professional knowledge, bachelor degree or above, familiar with the production workshop operating procedures;
2. Having experience in production and management of pharmaceutical companies for more than 5 years, prioritizing GMP workshop management experience;
3, excellent execution and communication skills; good professionalism, sense of responsibility, professionalism;
4, can adapt to long-term business trips.

QA Manager

Job Responsibilities:
1. Collect timely and understand the laws and regulations of the country regarding the quality management of pharmaceutical production, and formulate and implement the implementation plan;
2. Responsible for the construction of the quality management system, taking GMP as the standard, perfecting the quality management system, regularly organizing self-inspection, and ensuring the effective operation of the system
3. Organize the implementation of GMP, EU certification, FDA declaration, certification and specification;
4. To carry out comprehensive quality supervision and management of the production process, together with relevant departments to audit suppliers' quality system, review product process rules, and formulate quality monitoring points for each variety;
5.Provide quality support during external audits or inspections by customers and drug regulatory agencies and implement appropriate corrective and preventive actions
6. Formulate internal control standards for enterprise product quality in accordance with national standards, manage the release of products, and organize inspections for product stability
7. Responsible for monthly trend analysis of quality data and monthly product quality report, formulate product quality review report and propose corresponding corrective and preventive measures
8. investigation and tracking deviations and non-conforming material processing;

9. Responsible for reviewing the quality-related documents drafted by the production department and production workshops, and supervising the production departments, production workshops and product quality related work;
10. Responsible for quality training and education of all employees and guidance and supervision of subordinates;
11. Complete other tasks assigned by the leader.
job requirements
1.GMP and FDA or EU certification work experience;
2.Bachelor degree or above in pharmacy-related fields
3.More than 8 years experience in large and medium-sized pharmaceutical companies, more than 5 years of management experience, able to analyze and summarize work experience to guide production and scientific research.

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