Novo Nordisk
Senior QS Professional
Fuldtid
Permanent
2880 Bagsværd, Danmark
ID: 2713501
|
Indrykket for 7 dage siden
Are you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment.
Apply now and join Novo Nordisk.
Together we can create life-changing innovation.
Together we can make it happen.
The position Key areas of responsibility 主要工作职责 :
Input to site quality management review, including but not limited preparation of DV, CAPA, QMT, CR, CC, and Q-Case trend reports for management review.
DV 、 CAPA 、 QMT, CR, CC 和 Q-Case 等的趋势报告供管理层审核。 Support Site self-inspection and support corporate internal quality audit and external inspections including HA inspections at site.
HA 审计在内的外部审计。 Establish SOPs for quality related processes and procedures where relevant.
SOP 。 Provide quality management system related training to employees timely.
Monitor quality system key performance indicators.
Drive or support Quality initiatives 。 推动或支持质量部的各种活动。 Coordinate QS or regulation affairs related issues.
Approve or support approval of quality documents, e.g.
SOPs, DV, CR… 批批准或协助批准质量文件,如 SOP , DV , CR 等。 Maintain Customer Complaint (CC) handling process in STJ and monitor CC related data.
Organize or support CC related investigation and communicate to stakeholders including external stakeholders like NN BJ affiliate, health authority… 组织或支持 CC 相关的调查并与相关方保持沟通,包括外部相关方,如 NN 北京办公室,监管机构等。 Qualifications 4-yr (BS) Degree or above in Pharmaceuticals, Engineering or related field 药学、工程学或其他相关领域学科 4 年本科教育学士学位或以上 Fluent in written and spoken English 良好的英语书写和沟通能力 Minimum 5 years of experience related to quality in pharmaceutical or medical device manufacturing industry or working in a similar position.
5 年制药或者医疗器械制造行业质量相关岗位工作经验。 Previous experience with quality system, quality assurance, ISO, ISO, cGMP , EMA and FDA quality system regulation.
ISO, ISO, cGMP 法规 EMA 和 FDA 质量系统法规。 Prefer experience of customer complaint handling, or post market surveillance in pharmaceutical or medical device industry.
Working at Novo Nordisk At Novo Nordisk we recognise that it is no longer good enough to aspire to be the best company in the world.
We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures.
We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and the communities we operate in.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
We are happy to discuss flexible working, depending on the role and subject to business needs.
Are you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment.
Apply now and join Novo Nordisk.
Together we can create life-changing innovation.
Together we can make it happen.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world.
We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures.
We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in.
Together, we’re life changing.
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