工作职责：

1.  严格按照gmp、sop规定完成下达的生产任务。

2.  负责进行领浆、融浆、及投浆等工作。

3.  负责人血白蛋白及球蛋白类制品反应制作工作。

4.  负责人血白蛋白及球蛋白类制品组分沉淀分离工作。

5.  负责人血白蛋白及球蛋白类制品精制过滤操作工作。

6.  负责反应罐、管道、压滤机、不锈钢桶等生产设备和生产器具的清洗与消毒。

7.  负责状态标识的标示，批生产记录以及现场记录的填写。

8.  负责生产设备及仪器、生产用具等的日常维护、保养和管理。

9.  完成公司及部门安排的其他工作任务。

任职要求：

1.  大专及以上学历。

2.  服从工作安排。

3.  从事过药品生产工作者优先。

4.  一定的沟通能力。

5.  较强的团队合作能力。

6.  良好的写作能力。

工作职责：
1.support r&d project management to perform online research on diseases.
2.collect key competitors’ information using published information.
3.perform evaluation on medical devices.

任职要求：
1.university student. no experience required. biology, pharmaceutical sciences, biochemistry, nursing, medical related majors preferred.
2.ms word, excel, powerpoint.
3.academic journal research.

main acｃｏｕｎｔabilities:

1. contribute to the development of the ｃｏｕｎｔry medical plan

2. compliant implementation of assigned ｄｅｌiverables as defined in the ｃｏｕｎｔry
medical operational plan

3. closely collaborate with colleagues in the development and implementation
of the local strategy

4. closely collaborate with partner on the strategies and plans to ensure
effective ｅｘｅｃution towards achieving company objectives

5. establish effective clinical engagement with external medical experts,
hcps, scientific societies, scientific associations

6. map national kols in respective therapeutic areas, develop and train
national speakers

7. compliant ｅｘｅｃution of data generation activities

8. compliant management of research grants (incl. investigator-initiated
studies)

9. management of projects budget

10. medical accuracy of ｃｏｕｎｔry promotional and medical materials

11. manage product safety and regulatory requirements







tasks:

- develop and maintain up to date scientific and medical knowledge and
expertise (ta and products)

- bring therapeutic area knowledge and medical insights to msl team and
cross-functional teams

- ensure close and regular collaboration with product managers and market
access to support implementation of ｃｏｕｎｔry brand plans

- ensure close collaboration with regulatory affairs to support local
registration activities

- closely collaborate with msl team in the development and implementation of
pbm plan

- implement assigned ｄｅｌiverables of annual ｃｏｕｎｔry medical plan

- plan and track budget for assigned ｄｅｌiverables

- identify, develop and maintain effective engagement with external medical
experts and hcps

- support implementation of access strategy to assure access

- support ｅｘｅｃution of local data generation activities

- manage research grants (incl. investigator-initiated studies)

- implement assigned ｄｅｌiverables of medical communication plan, e.g. disease
awareness, medical education, and ｃｏｕｎｔry congress activities

- implement assigned ｄｅｌiverables of local publication plans, including local
congresses and manuｓｃｒｉｐｔs

- ｄｅｌiver medical training to field based medical team and other local staff,
e.g. sales reps

- timely respond to medical enquiries escalated by local medical information
staff

- support local medical information staff with development and maintenance of
local key information documents (lkid)

- ensure compliance with applicable local and global laws, regulations,
guiｄｅｌines and company policies and procedures in all activities

- review of local materials

- manage product-related safety issues for provide input to the area
compliance person

- ａｄｄitional scope of responsibilities and other therapeutic areas may be
assigned by the medical head

- closely monitor regulatory environment changes and competitor information
and provide timely ｕｐｄａｔｅs with interpretation and impact analysis




qualifications:

minimum requirements

· university degree in medical or life science field (e.g. medicine, pharmacy,
biology/ biochemistry)

· clinical patient contact experience or minimum of 2 years’ experience with
pharma industry in medical affairs (e.g. medical information or field medical
role) and/ or clinical

· excellent oral and written communication skills in chinese/mandarin and very
good oral and written communication skills in english

preferred requirements

· medical education (md) or pharmacy degree (pharmd), phd in life science
field (e.g. biology/ biochemistry)

· medical specialization and/ or clinical / research experience in internal
medicine, nephrology or cardiology

· clinical patient contact experience and minimum of 2 years’ experience with
pharma industry in medical affairs and/ or clinical development

· publication track record

· fluent in chinese/mandarin and english (verbal and writing)