M&S-Sterile Production Technician-Beijing at Sanofi Aventis US LLC

Beijing, Beijing, China -

Full Time

Start Date

Immediate

Expiry Date

10 Apr, 26

Salary

0.0

Posted On

11 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Systems, Aseptic Processes, Regulatory Requirements, Communication Skills, Decision Making, Manufacturing Processes

Industry

Pharmaceutical Manufacturing

Description

Job Information职位信息 Job title职位名称: Sterile Production Specialist Location工作地点： Beijing北京 Job type工作类型: Permanent长期 Site/Unit 区域/事业部：赛诺菲（北京）制药有限公司 Sanofi (Beijing) Pharmaceuticals Co., Ltd About the job工作职责 We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as CSV Engineer within our M&S China-BEI Site, will be to making best class medicines with excellent strategies and tools and delivering them to our patients. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? Main responsibilities职责描述： Please indicate here the main job responsibilities请列举该职位的主要工作职责。 Generic 通用 1. Assist dept. manager to coordination of Project, plan, Quality and engineering to organise production with right volume, right quality, right cost and on right time. Supervise production, human resources, facilities to ensure all activities comply with China GMP and Sanofi regulations. Keep continuously improvement in terms of safety, quality, cost, delivery, motivation and environment. 协助部门经理有效协调项目、计划、质量、工程等资源，按时保质保量地组织生产。有效监控生产活动、人员、设备设施确保所有生产活动和过程符合中国GMP和赛诺菲内部规范的要求，推动安全、质量、成本、生产任务的达成、激励和环境方面的改善。 2. Continuously improve the compliance level of sterile production, attend and promote SMS execution, Lean manufacturing. 3. 不断提高无菌生产的法规符合性和质量保证水平，参与并推进赛诺菲制造体系的深度实施和部门的精益生产。 4. Organize, coordinate, track and implement of deviations, changes, validation, complaints and global standards gap analysis etc. 5. 组织、协调、跟进和实施偏差、变更、验证、投诉以及总部标准差距分析。 6. To ensure the continuous process compliance improvement through the management of quality systems. 7. 通过质量体系的管理确保生产工艺合规的持续改进。 8. To ensure the implement of quality policy/objectives of Sanofi and to ensure the quality compliance of sterile production operation. 9. 贯彻执行公司的质量方针和质量目标，确保无菌生产运营的质量合规性。 10. To ensure effectiveness of sterile production quality improvement programs/projects. 确保无菌生产运营的质量改进计划或项目的有效性 KEY ACCOUNTABILITI关键职责 1. Perform the job duties of the Inspection Process-Centric Unit. 履行灯检PCU工作职责 -Takes responsibility for the 24h performance of the Level 1 Operating Unit and defines priorities for the day/week/month. 负责1级操作层面的24h绩效，并制定日常日/周/月的工作优先级。 -Ensure that standards of SMS2.0 are followed (incl. Role cards, standard workplan, planning adherence, standard times, Asset Care activities. 确保遵循 SMS2.0 的标准（包括角色卡、标准工作计划、计划遵守情况、标准时间、资产维护活动。 -Make sure that improvements opportunities on the assets/processes/scheduling are correctly escalated and contribute to CI. 确保资产/工艺/计划上的改进机会并正确上报，并为持续改进做出贡献。 -Attend to and lead Level 1 meetings (+QDCI Level 1, CI Level 1, Asset care, Deviation management, E2E flow...). 参加并领导 1 级和 2 级会议（+QDCI 1 级、CI 1 级、资产维护、偏差管理、E2E 流程...... -Reviews performance and contributes to upskilling PCU members. 审查绩效并有助于提高 PCU 成员的技能。 2. Responsible for the shift work of PCU production (morning, middle and night). 负责PCU生产现场倒班（早、中、夜）工作。 3. Participate in process optimization, equipment improvement and technique innovation to sustainably improve OEE and yield, participate in SMS standards deep execution and continuously improve in 5S/HSE aspects and waste minimization. 参与工艺优化、设备改进和技术创新，持续提高产品收率和设备利用率，参与赛诺菲制造系统标准的贯彻落实，在HSE、精益生产等方面持续改进。 4. Optimize the production process, improve the equipment and system, consistently supply high quality production for commercial operation preparation 优化生产工艺，改进设备和系统，保证始终如一地生产出合格产品，为正式商业运作的准备。 5. Sustainably improve yield of compounding, filling and inspection equipment and ensure the stable supply to the market. 持续提高配制工艺收率，保证市场稳定供应。 6. Management of the production environment, process, hygiene, facilities to make sure all production activities comply with drug master file, SOPs and GMP requirements. 生产环境、工艺、卫生、设施等的管理，确保生产活动符合工艺规程、SOP和GMP要求。 7. To review the batch production records and submit to Quality in time. 审核批生产记录，及时送交质量部门。 8. To implement the equipment qualification, process validation according to the master plan. 按照计划执行完成区域内的设备的确认和工艺验证。 9. To execute and follow the required initial and continuous trainings of production operators. 对生产相关人员进行必要的上岗前培训和继续培训，并根据实际需要调整培训内容。 10. Organize daily production meeting, coordinate all shifts and keep closely communication with planning, QA, maintenance and warehouse etc., to implement production plan strictly and ensure right Plant Service Level and Bias. 组织日常生产协调会，协调各生产班组的活动及与质量、计划、维修、仓库间的沟通，严格执行生产计划，确保生产计划完成率及生产计划符合性。 11. Follow up the actions of Change Control, CAPA for deviations or complaints related to production. 确保生产中所有变更、偏差及生产相关的投诉问题纠正措施和预防措施的及时落实及有效性。 12. Develop necessary SOPs and ensure the implementation and improvement. 组织制定相关的岗位操作规程并确保执行及持继改进。 13. Implement SMS standards and continuously improve in 5S/HSE aspects and waste minimization. 贯彻落实赛诺菲制造系统标准，在HSE、精益生产等方面持续改进。 14. Report product complaints and adverse drug reactions according SOP requirements. 根据SOP要求报告产品投诉和药物不良反应。 15. Other tasks temporarily assigned by department manager. 按时完成上级临时交办的或部门间合作的其他工作任务。 Sterile production Department HSE Responsibilities 无菌生产部HSE职责 ➤ Responsible for following the company’s HSE policy and integrated all requires into daily job. 负责贯彻公司HSE的有关规定，把公司HSE制度的措施贯彻到每个具体环节。 ➤Incorporate HSE work into the work plan 将HSE工作纳入工作计划中。 ➤ Organize the implementation of HSE management target plan of this department, implement HSE rules and regulations, HSE operation procedures and HSE technical action plan. 组织实施本部门HSE管理目标计划，落实HSE规章制度、HSE操作规程和HSE技术措施计划。 ➤Regularly carry out to identify HSE potential hazards and develop action plan and finish on time. 定期开展本部门HSE隐患排查治理工作，制定整改计划并按时完成隐患整改。 ➤Timely working out of employee opinions. 负责部门级HSE教育与考核工作，及时处理员工提出的意见。 ➤Actively cooperate with HSE management to prevent accidents happens. 积极配合HSE管理工作，防止各类事故的发生。 ➤ Regularly carry out +QDCI meetings at all levels considering HSE8 requirements. Feedback HSE issues in a timely and accurate manner, and actively implement remediation. 定期开展本部门各级+QDCI会议，结合HSE8要求，及时、正确填写和反馈各类HSE问题，并积极落实整改。 ➤Participate in the investigation for accidents, analyze the root causes of accidents from the quality management perspective, and related CAPA. 参加事故调查分析工作，从质量管理角度分析事故原因，提出事故防范措施。 ➤Responsible for design annual department PASS plan and ensure implementation as planned. 负责制定年度部门PASS计划，并按进度组织实施。 Sanofi (Beijing) Pharmaceutical Co., Ltd. Energy Policy: "Quality as the top priority, through technical, behavioral, human consciousness, continuously reduce the rate of energy consumption in product value, benefit the users, and promote company development". Good awareness of energy conservation is required, participate in energy saving actions, and assist in the continuous development of the energy management system. 赛诺菲（北京）制药有限公司能源方针：“以药品质量为第一要务，通过技术手段，行为规范，人为意识，不断降低产品价值中的能耗比重，造福广大用户，促进企业发展”要求每位员工具有良好的节能意识，积极的节能行动，协助能源管理体系的持续开展 ➤ Actively propose energy-saving projects 积极提出节能方案 ➤ Coordinate and support the development of energy-saving projects and give positive feedback 协调并支持节能项目的制定，积极反馈意见 ➤ Coordinate and participate in the implementation of energy-saving projects 协调并参与节能项目的执行 ➤ Participate in internal audit of energy management system About you 任职资格: List here ideally the must-haves criteria to be successful on the role. 请列出胜任该职位所必须具备的条件。 At least a bachelor or above degree in pharmacy or biology disciplines with 0~2 years’ experience in quality or sterile area. Must be a committed "Quality or Sterile" professional with knowledge of quality systems within the pharmaceutical or related industry. 至少药学或生物学相关专业大学本科及以上学历， 0~2年质量或无菌领域工作经验。必须具备制药或相关行业的质量体系的“质量或无菌”专业知识经验。 •Thorough understanding of manufacturing processes and aseptic processes 全面理解生产流程和无菌工艺 •Strong working knowledge of quality systems, regulatory requirements across multiple health authorities. 质量系统和各相关法规要求等方面具有工作经验。 •Fluent English both in written and verbal 熟练的英语口语与书写能力 •Good communication skills 良好的沟通能力 •Able to burden pressure 能够耐受压力 •Brave to make decision 果敢决策 Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave. Pursue Progress. Discover Extraordinary. Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! Global Terms & Conditions and Data Privacy Statement Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting www.sanofi.com or via our movie We are Sanofi As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live. All in for Diversity, Equity and Inclusion at Sanofi - YouTube

Responsibilities

The Sterile Production Technician will assist in coordinating production activities to ensure compliance with quality standards and regulations. They will also be responsible for continuous improvement in sterile production processes and managing quality systems.