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Salary
≈ $13k – $24k per year (Estimated)
Location
In office (Taicang)
Seniority
Intern
Employment
Internship

Confirmed on the employer's own hiring board on Oct 24, 2026. First seen by Alion on Oct 13, 2026. Revvity scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Revvity is a US life sciences and diagnostics company headquartered in Waltham, Massachusetts, that supplies instruments, reagents, software and services for drug discovery, research, newborn and prenatal screening and clinical diagnostics. It is the former PerkinElmer Inc., renamed in 2023 after selling its analytical and enterprise services businesses, and today employs more than 11,000 people worldwide and also runs the ViaCord newborn stem cell banking service. It hires field service and customer support engineers, field application and R&D scientists in bioprocessing and gene editing, sales specialists and account managers, AI and DevOps engineers, and finance, legal and HR staff.

Job Title

Intern/Student

Location(s)

Taicang (Suzhou)

About Us

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.

Find your future at Revvity

  • 协助完成文件受控、记录核查、供应商档案与组件图纸的日常维护。
  • 配合跟进偏差、变更、CAPA、客诉、退货等事项的处理进度 。
  • 参与跨部门资料传递与信息沟通(含与委托生产企业的对接)。
  • 协助质量数据的收集整理,以及年报、自查报告等监管申报材料的准备。
  • 协助法规/标准等外来文件的整理与质量培训的组织。
  • 完成主管交办的其他日常支持工作。
  • Assist with document control activities, including maintenance of controlled documents, review of records for completeness and accuracy, and upkeep of supplier files and component drawings.
  • Support tracking and follow-up of quality events, including deviations, change controls, CAPAs, customer complaints and product returns, to ensure timely closure of action items.
  • Facilitate cross-departmental documentation and information exchange, including liaison with contract manufacturers.
  • Compile and maintain quality data, and assist in the preparation of regulatory submissions, including annual reports and self-inspection reports.
  • Assist in the administration of external documents, such as applicable laws, regulations and standards, and support the coordination of quality training activities.
  • Perform other routine duties and ad hoc tasks as assigned by the supervisor.
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