Rosso Development

Founded in Shenzhen, China in 2006, Rosso has grown into a professional pharmaceutical company focused in Chinese market, with the sales growth rate of over 35% annually. Following the global development trend of the pharmaceutical industry and identifying the Chinese market demands, Rosso has won an ever-growing reputation of our solid performance, persistence and dedication among industry friends. Rosso has established firm relationships with several famous overseas manufacturers within these few years, and together achieved ongoing success.

Rosso Operations

Our leaders have experience of two decades in pharmaceutical marketing, the in-house sales channel is spread out over the country, and our full-time sales representatives exceed 280. With the assistance of our professional team and rich experiences in self-operation, surely you will receive a satisfying result. We create and optimize the project plan, fully develop the target market, in order to achieve sales goals; meanwhile we keep exploiting new territories and make prompt adjustments to the market strategies, thereby increase the value of your assets and improve the returns.

Registration Service

In the purpose of obtaining long-term success of your products in China, and have the sales maintain stable growth, Rosso is also able to provide you with service of regulatory affairs for your pharmaceutical products in mainland China. We have a professional team of regulatory affairs, who evaluate the product registration dossiers for you, apply for new drug license under your authorization, make efforts to ensure the success of license renewal and solve other problems regarding regulatory affairs.

MISSIONS AND VALUES

Mission

Devoted to build up a top Chinese pharmaceutical enterprise which brings welfare to patients, create values for clients, offers opportunities of personnel development for staff and introduce pharmaceutical products of high cost effectiveness for human health.

Integrity

Rosso is one the very few CSOs in mainland China focused in importing and marketing imported drugs. As the exclusive agent of imported drugs, we have maintained years of stable cooperation with several famous global pharmaceutical manufacturers from Germany, Japan, Taiwan, etc. Our rich experience and numerous successful cases have won recognition and reliance from our clients, and enjoyed a high reputation in the Chinese healthcare field. In the future, we sincerely hope to establish long-term collaboration with more excellent manufacturers. We will be your most reliable partner in the Chinese pharmaceutical market.

Professional

Rosso keeps building and improving our professional clinical promoter team, completing the layout and integration of the domestic market. We carry out academic promotion in the most influential hospitals in the major cities, and keep connected well with academic association and societies; moreover, we cooperate with major hospitals annually to conduct clinical studies, further expand the application territories of the product or inspect its safety. Besides, our professional regulatory affairs team is competent to offer you a safe and comprehensive registration service, and can undertake pre-launch new drug license application and post-launch follow-ups of any regulatory affairs.

WHAT WE DO

Regulatory affairs

Rosso’s regulatory affair team is offering you safe and comprehensive registration agent service. We can undertake regulatory affairs for imported products including new license application, license renewal, etc. The team is led by experts engaged in regulatory affairs for years, with deep understanding in China regulatory policies, are capable to accurately evaluate the product upon their rich experiences of successful applications. We customize the application of your product according to its features and make the optimal registration scheme for it; meanwhile we keep constant communication with senior consultants, have the application re-evaluated, and make prompt adjustments to the strategies, which, in all aspects, will enhance the success rate of new registration, renewal and alterations for your products.

Product analysis

Rosso commit ourselves to selecting products with the advanced therapeutic concept and excellent quality, and even better if can be assorted with our current product lines. Through our existing national KOL network established over the years, Rosso is able to acknowledge the practical demand of clinical use and keep track of the market dynamic of Chinese medical industry. Rosso’s marketing department will find the precise position for your product and the entry point that suits it best in China, and scheme out the optimal marketing channel.

Staff training

The leaders in Rosso sales team are senior in pharmaceutical business for almost 2 decades, followed by sales representatives who devoted into their work with high efficiency. The present sales reps, 90% of which are educated in medical and pharmaceutical major, with solid foundation of academic knowledge, receive specific product trainings at least twice a year, constantly learning to improve knowledge related to products and the industry, for further understanding the products, and even exploring new product features and new opportunities..Rosso has established talent development program of pharmaceutical sales and management with several professional training organizations in the industry. For Rosso, work force is resource instead of cost. We integrate employees’ personal pursuit into the long-term development of our company, which will not only raise the vocational level of our staff in the business, but also provide stages for them to perform their talents. Rosso cherishes each of our staff.

Marketing

As one of the main promoters of imported drugs in China, Rosso excels at marketing planning, academic promotion at national level and brand building, achieving our mutual development and marketing objectives. In compliance with laws, regulations, administrative rules and standards, we create and optimize your project plans, with our holistic marketing and multi channels, through our sales network the products will rapidly enter the Chinese market, and by continuous academic promotions it will reach the expected market position and shares.Rosso not only give you promise of a steady sales growth, but also will keep looking for new opportunities and digging new selling points, constantly develop new markets, in order to renew your “old” products.

HISTORY

JOIN US

简历投递邮箱：[email protected],请注明应聘职位，工作地点，薪资待遇。
机修工负责公司生产基地内各设备仪器的维修、维保等工作；领导分配的其他工作。
1、熟悉制药企业工作模式，有6年及以上制药企业设备维修经验；
2、动手能力强，能够快速、准确判断生产设备故障并进行分析和处理；
3、有焊工证、电工证；
4、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
电工负责配电房值守；负责公司压空系统操作，冷水机组操作；负责工厂工程维修相关事务；领导分配的其他工作。
1、高中或中专以上学历；
2、熟悉自动化设备控制原理及相关电气知识；
3、具有控制电路故障判断及分析能力，并能快速对故障进行排查；
4、熟悉自动化设备机械结构原理，能根据CAD机械图纸完成装配；
5、熟悉常规电器控制，配电房系统，二次回路控制；
6、会根据变频器说明书调参数，具有理论知识，了解PLC和人机界面，不需要编程；
7、持有电工特种作业操作证；
8、具有配电房值班工作经历，倒闸、送闸、断闸实际操作工作经历；
9、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
车间工艺员负责车间现场管理，进入车间生产第一线，发现和处理生产过程中的技术问题和安全隐患，对车间工艺纪律和产品质量负责；负责车间相关GMP文件的起草及实施；负责指导和监督车间严格按照GMP组织生产，防止混淆和差错；负责指导和监督各岗位生产记录及二级记录填写，整理汇总相关生产记录，并归档；负责建立生产台账；负责召开车间质量分析会；负责组织车间技术及质量等相关GMP培训工作；负责偏差和异常情况调查，提出解决方案并执行；负责车间工艺技术攻关等工作；负责车间相关工艺验证和清洗验证等工作；领导分配的其他工作。
1、药学相关专业，本科及以上学历；
2、有药厂生产管理和工艺技术相关工作经验有优先；
3、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
QC（理化+仪分）对所有进厂物料、中间产品、待包装产品、成品等严格按照操作规定进行检验，及时填写检验记录，保证检验结果的准确性和及时性；起草本岗位所用仪器设备确认与验证，分析方法的验证、确认、转移方案，执行仪器校验和分析方法确认与验证任务；起草、修订本岗位的相关文件（包括但不限于质量标准、检验SOP、检验记录）；负责公用系统（如纯化水系统、压缩空气系统等）验证及日常监测； 负责实验室仪器、设备的管理并做好清洁及维护、保养工作；负责本岗位检验结果的统计和总结，作好信息反馈工作；严格认真执行GMP文件，一旦发现与文件不符或有异
1、熟悉药品生产相关药典、GMP等标准规范；
2、熟练掌握常见药品的检验项目和方法，熟悉常见理化、仪分仪器设备的操作和维护，熟悉试剂试液的性质；
3、专科及以上学历，至少2年以上药品检验相关工作经验，有制药行业背景；
4、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
现场QA负责车间、库房、QC、公用系统等区域的现场监控； 负责中间产品中控项目测试；负责车间洁净度监测，水系统、物料、产品等的取样工作；领导分配的其他工作。
1、统招大专及以上学历，药学等相关专业毕业；
2、熟悉药品生产过程，熟悉GMP等规范要求；
3、具有化学药品生产和质量管理经验；
4、能熟练操作天平、崩解仪、检漏仪等各仪器；
5、沟通表达能力强、学习能力强，能熟练操作各种办公软件；
6、能接受中班或夜班（根据生产任务调整安排）；
7、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
体系QA负责文件管理、培训管理、验证管理，偏差、变更、CAPA、投诉召回、自检、药物警戒、供应商管理等一个或多具体上级安排的质量要素管理工作；负责各类审计迎审和缺陷项整改回复；负责建立和管理产品质量档案，负责产品年度质量回顾；参与批生产记录、批检验记录审核、产品放行审核协助工作；完成上级交办的其它工作。
1、熟悉药品生产相关法律法规和药典、GMP等标准规范，熟悉质量管理要素并能有效实施；
2、掌握质量管理工具及手法，了解固体制剂、软膏剂、注射剂等产品工艺流程和产品标准；
3、具有较强的计划、组织、协调、沟通和执行能力；
4、本科及以上学历，至少1年及以上质量管理相关工作经验，有制药行业背景；
5、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
QA经理指导、贯彻、落实企业的质量方针和质量目标，负责公司质量管理体系的完善并确保有效运行；负责GMP相关许可检查、符合性检查迎审工作，负责定期和不定期组织召开公司质量分析会议；组织和完成公司变更控制与偏差处理、不合格品处理、投诉/召回处理、验证管理、计量管理、供应商管理、培训、自检、质量回顾、电子监管等工作，保障现场监控的有力执行；负责批生产记录审核、产品放行审核协助工作；领导分配的其他工作。
1、熟悉药品生产相关法律法规和药典、GMP等标准规范；熟悉质量管理要素并能有效实施；
2、掌握质量管理工具及手法，了解固体制剂、软膏剂、注射剂等产品工艺流程和产品标准；
3、具有较强的计划、组织、协调、沟通和执行能力；
4、本科及以上学历，至少5年以上质量管理相关工作经验，有制药行业背景；
5、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
QA主管指导、贯彻、落实企业的质量方针和质量目标，负责公司质量管理体系的完善并确保有效运行；负责GMP相关许可检查、符合性检查迎审工作，负责定期和不定期组织召开公司质量分析会议；组织和完成公司变更控制与偏差处理、不合格品处理、投诉/召回处理、验证管理、计量管理、供应商管理、培训、自检、质量回顾、电子监管等工作，保障现场监控的有力执行；负责批生产记录审核、产品放行审核协助工作；领导分配的其他工作。
1、熟悉药品生产相关法律法规和药典、GMP等标准规范；熟悉质量管理要素并能有效实施；
2、掌握质量管理工具及手法，了解固体制剂、软膏剂、注射剂等产品工艺流程和产品标准；
3、具有较强的计划、组织、协调、沟通和执行能力；
4、本科及以上学历，至少3年以上质量管理相关工作经验，有制药行业背景；
5、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
车间主任负责公司口服液等液体制剂、软膏剂车间的车间管理工作，对车间生产的产品质量负责，确保产品质量符合生产要求及相关标准；负责车间相关制度、文件的编写及执行；负责车间人员行为规范、生产操作规范的管理；对车间各岗位所用物料的存放以及使用的正确性把关，确保物料符合质量标准；负责车间的安全生产，确保生产现场的安全；对生产现场生产设备等的各种状态标识负责，确保标识的准确性和设备的正常运行；领导交办的其他工作。
1、本科及以上学历，药学、化学等相关专业；
2、熟悉药品生产相关法律法规和药典、GMP等标准规范；
3、有口服液等液体制剂、软膏剂等产品生产车间管理经验；
4、具有较强的计划、组织、协调、沟通和执行能力；
5、至少2年及以上生产车间管理相关工作经验，有制药行业背景；
6、工作地点：四川省眉山市东坡区尚义镇玉桂路16号（西部药谷）。
制剂研究员负责制剂项目调研，并能独立撰写调研报告；负责制剂小试、放大、工艺验证等实验的方案起草与执行，并撰写总结报告；负责解决项目过程中出现的问题；负责撰写完成BE相关文件及制剂申报资料；负责制剂实验室日常管理；完成上级安排的各项事宜；
1、药学及制药等相关专业，本科及以上学历；
2、有5年及以上制剂项目研发工作经历；
3、有3个及以上制剂项目的申报经验，其中有1个项目获批生产经验者优先；
4、熟悉口服固体、液体等常规制剂剂型，及相关实验设备操作和维护；
5、具备良好的专业素质、优秀的沟通协调能力、较好的团队协作能力、有较好的工作态度和敬业精神；
6、工作地点：四川省成都市高新西区百草路1018号（成都恒瑞制药内）。