职位
Technical and Functional
Complete adroitly the assigned routine inspection of sample, issue the
reliable analytical report in reasonable Lead-time.
· By master analytical methods within working section, comply with
professional morality and etiquette to ensure reliability and integrity of the
analytical data and keeping the excellent capacity of working suitability.
· By rationalize time allocation, optimizing combination the samples in
hand, to keeping the reasonable lead-time.
· By form a good working habit to standardize experimental operations.
· By checking analytical result serious and careful to minimize mistakes
and ensure accuracy and reliability of testing figures.
Implement GMP compliance against global GMP standards and China GMP requirement
· By assisting lab. Manager to conduct GMP Self- Inspection, and follow-up
the implementation action to maintain the global level of GMP compliance.
· By maintaining the quality system and documentation system to ensure
quality system operations in QC meets the regulatory.
Implement the maintenance and calibration of assigned instruments
· By accomplish the calibration and maintenance of assigned instruments, to
ensure they are in good order to meet the analytical needs any time.
· By keeping the relevant document to trace the calibration, maintenance
history and any change of the instruments.
· By keeping contact with instrument company to obtain the sufficient
application technical support.
· By keeping contact with instrument company to obtain the repair service
in time.
· Report the abnormal status, unexpected results to supervisors with
initiative and in time.
· By reporting abnormal status and unexpected results during analysis
processing at first time by detailed data and information to alert supervisor
to investigate and solve the problem in correct way and in time.
· By involving the investigation, precession to provide actual data and
information to helping to provide the same issue happened repeatedly.
· By providing technical support to analyst, if necessary share knowledge
and experience within working section.
Stick lab safety regulations to prevent occurrence of accident.
· By obey the safety instruction of the storage, usage and disposal of
reagent, narcotics, medicines, lab waste.
· By following the usage instruction of facilities of water, electricity,
steam and etc. in lab.
· By clearing the working space in time to follow company safety rule, and
patrol working section at the end of working day to secure the safety of lab.
Implement the analysis method validation.
· By implement the assigned analysis method validation according to
validation plan.
· Sampling of cleaning validation.
Have the ability to find and solve the problems occurred in the routine work.
· To find the problems and solve the problems in correct way and in time
during the analysis processing.
· To ensure the normal running of routine work.
Qualification and Experience
Education/Qualifications
· Bachelor’s Degree (biology, microbiology, biochemistry, chemistry or
other relevant discipline is preferred)
· Graduate or higher-level Degree is preferred
Leadership Competencies
· 3 or more years’ work experience in the pharmaceutical or related industry
· 3 or more years’ quality, compliance or other relevant experience in the
pharmaceutical industry
我们是谁
在罗氏，来自100个国家的100，000名员工不断推动着健康医疗行业的进步。我们一同工作，使罗氏成为了世界领先的以研发为基础的健康医疗集团。我们的成功源于创新、求知和多元化，也源于我们把相互间的差异作为一种优势。为了革新医疗健康领域，罗氏设定了远大的计划，坚持学习和发展，并不断寻找与之志同道合的伙伴。
罗氏中国由制药和诊断两大业务领域组成，员工总数超过7000人。作为全球个体化医疗的领导者，罗氏制药和罗氏诊断均在中国建成了完整的价值产业链，包括研究、开发、生产、营销等环节。未来，上海将成为罗氏继巴塞尔和旧金山之后的第三大全球战略中心，而罗氏也将继续践行对中国的长期承诺，满足中国患者的未尽之需。
罗氏提供平等的职业发展机会。