REQ-10079050
May 27, 2026
LOC_CN

About the Role

Major Accountabilities
主要职责


  • Provide QA oversight for routine operational activities to ensure compliance with approved procedures and regulatory requirements.
    对日常运营活动提供质量保证监督,确保其符合已批准的流程和法规要求。
  • Review master batch document, operational documents, logbooks, forms, and other GMP-related documentation.
    审核主批记录、运营相关文件、日志、表格及其他与GMP相关的文件。
  • Support the management of deviations, non-conformances, investigations, root cause analysis, CAPA, and change controls.
    支持偏差、不符合项、调查、根本原因分析、纠正预防措施及变更控制的管理。
  • Ensure timely review, closure, and follow-up of quality events and quality system records.
    确保质量事件和质量体系记录得到及时审核、关闭和跟进。
  • Participate in internal audits, external audits, regulatory inspections, and customer audits as required.
    根据需要参与内部审计、外部审计、法规检查及客户审计。
  • Monitor compliance with Good Manufacturing Practices, Good Documentation Practices, and company quality standards.
    监督良好生产规范、良好文件规范及公司质量标准的符合性。
  • Support the development, review, and revision of SOPs, work instructions, forms, and other GMP document.
    支持标准操作规程、工作指导书、表格及其他GMP文件的制定、审核和修订。
  • Provide QA support for product release activities, including documentation review and compliance checks.
    为产品放行活动提供质量保证支持,包括文件审核和合规性检查。
  • Collaborate with cross-functional teams to resolve quality issues and implement process improvements.
    与跨部门团队合作,解决质量问题并实施流程改进。
  • Track and report quality metrics, trends, and key performance indicators.
    跟踪并汇报质量指标、趋势及关键绩效指标。
  • Support training activities related to quality systems, GMP compliance, documentation practices, and procedural updates.
    支持与质量体系、GMP合规、文件规范及程序更新相关的培训活动。
  • Ensure that quality risks are identified, assessed, escalated, and mitigated appropriately.
    确保质量风险得到识别、评估、升级和适当控制。
  • Assist in preparing quality reports, management review inputs, and audit readiness documentation.
    协助准备质量报告、管理评审资料及审计准备文件。
  • Mentor junior QA team members and provide guidance on quality processes and compliance expectations.
    指导初级质量保证团队成员,并就质量流程和合规要求提供支持。
  • Promote a culture of quality, compliance, and continuous improvement across the organization.
    在公司内部推动质量、合规和持续改进文化。

Key Performance Indicators
关键绩效指标


  • Execute product-related quality activities in a timely manner and in compliance with cGxP and registration requirements.

及时开展与产品相关的质量活动,并确保符合cGxP及注册要求。

  • Demonstrate positive performance trends across key quality management process indicators.

在关键质量管理流程指标方面展现出积极的绩效改善趋势。

  • Contribute effectively to continuous improvement projects that support quality and operational performance.

有效参与支持质量与运营绩效提升的持续改进项目


Education and Work Experience

教育背景和工作经验


  • Bachelor or master’s degree in Pharmacy, Chemistry, Biology, Microbiology, Life Sciences, or a related discipline.
    药学、化学、生物学、微生物学、生命科学或相关专业本科及以上学历。
  • Minimum of 3–5 years of experience in Quality Assurance, Quality Operations, pharmaceutical manufacturing operations or a related quality function.
    至少 3–5年 质量保证、质量运营、制药生产运营或相关质量职能工作经验。
  • Experience in a regulated industry such as pharmaceuticals, biotechnology, medical devices, food manufacturing, or healthcare products.
    具备制药、生物技术、医疗器械、食品制造或健康产品等受监管行业经验。
  • Strong understanding of GMP, GDP, quality systems, deviations, CAPA, change control, and audit processes.
    熟悉GMP、GDP、质量体系、偏差、CAPA、变更控制及审计流程。
  • Experience reviewing batch records, SOPs, validation /qualification documents, and operational quality documentation.
    具备审核批记录、标准操作规程、验证/确认文件及运营质量文件的经验。

Language
语言能力


  • Good (oral and written) in English; fluent in local language (oral and written)

良好的英语水平(口头和书面); 流利的当地语言(口头和书面)



Key Skills and Competency

关键技能与能力


  • Strong attention to details and commitment to compliance.
    注重细节,并高度重视合规要求。
  • Excellent written and verbal communication skills.
    具备优秀的书面和口头沟通能力。
  • Strong analytical, problem-solving and decision-making abilities.
    具备较强的分析、问题解决和决策能力。
  • Ability to manage multiple priorities and meet deadlines.
    能够同时管理多项任务并按时完成工作。
  • Effective collaboration with cross-functional teams.
    能够与跨部门团队进行高效协作。
  • Ability to work independently with minimal supervision.
    能够在较少监督下独立开展工作。
  • Strong leadership and mentoring skills.
    具备较强的领导力和指导能力。
  • High level of integrity, accountability, and professionalism.
    具备高度诚信、责任感和职业素养。

Role Requirements

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

DIV_TO
Quality
LOC_CN
Changping County (Beijing)
FCT_QA
Full time
正式
No
careers default image
REQ-10079050

Sr. QA Operations Specialist

Apply to Job