天津招聘

JOB SUMMARY

Primary responsibilities include managing regulatory compliance of quality system in accordance with ISO13485, FDA 21 CFR Part 820 and customer specific requirements. Provides quality assurance for product design and development project and managing internal, customer, third party or FDA quality audits, review and assist with Design History File and other project support documentation.

ESSENTIAL DUTIES AND RESPONSIBILITIES

1. Establish, implement, maintain and improve quality management system.

2.Maintain quality system documentation, plan quality system process, and implement internal quality audit.

3. Support customer, third party quality audits.

4. Develop and maintain Project Quality Assurance Plans and monitor product design project execution from quality perspectives.

5. Support the engineering team in the management and maintenance of design history file.

6. Provide direction and training to the employees on quality regulatory requirements

7. Be responsible for corrective and preventive actions and customer complaints.

8. Provide professional support on quality issues with the internal/external customer as needed.

9. Work with design engineering team, manufacturing, and project manager on quality aspects.

10.Prepare and present presentations related to quality improvement initiatives.

11. Provide regular updates to Quality Manager on the execution of quality assurance activities and highlight the risk with solution.

12. Comply and follow all procedures within the company security policy, environment, safety and health rules and regulations associated with this position.

13. May perform other duties and responsibilities as assigned.

MANAGEMENT & SUPERVISORY RESPONSIBILITIES

1. Typically reports to Management. Direct supervisor job title(s) typically include: Quality Systems Manager

2. Job is NOT directly responsible for managing other employees (e.g., hiring/termination and/or pay decisions, performance management).

JOB QUALIFICATIONS

KNOWLEDGE REQUIREMENTS

1. Quality Management System Standards and Regulations, 21CFR Part 820, ISO13485, ISO9001

2. Problem solving abilities and risk management knowledge, 8D, CAPA, FMEA, ISO14971

3. Team player and flexibility to deal with ongoing change and customer resistance

4. Proficiency in use of personal computers, Microsoft Office products (Excel, Word and PowerPoint) and e-mail skills required.

5. English communication both orally and in written.

6. Organize verbal and written ideas clearly and use an appropriate business style and quality thinking.

EDUCATION & EXPERIENCE REQUIREMENTS

1. Bachelor’s degree and five years experience.

2. Prefer experience in medical device manufacturing and automotive manufacturing

3. Experience in creating and implementing quality system and quality audit.

Jabil 是世界上***型的电子制造服务公司之一，为当今一些***型的公司和品牌提供定制设计、制造、配送和售后服务。我们的全球运营事业已拥有超过 3,700 万平方英尺的制造厂，遍及四大洲的 100 多家工厂，并已雇用 180,000 多名员工。

为确保我们能继续创造经济效益和增长，我们已在多个市场开展运营，包括售后服务、计算与存储、国防与航空、医疗与仪表制造、工业和清洁技术、材料技术、移动通信、网络和电信。此策略已取得成功 — 在十多年内，我们通过坚定不移地致力于适当结合服务、行业、位置、系统和人员，已取得了两位数的增长。Jabil 已使用 “JBL” 代码在纽约证券交易所上市，我们欢迎未来的员工查阅公司的财务概况。

我们为有资历的个人提供平等的雇用机会，无论其种族、宗教、肤色、年龄、国籍、性别、残疾和性取向如何。我们将员工技能、能力、经验和背景的多样化视为一项优势，并在 Jabil 的所有领域中鼓励发挥该优势。

我们主张聘用适当的人员、将他们安排在能贡献一己之力的职位，并为他们提供决策所需的工具和职权。如果您对所做的一切都秉持质量***的心态，且对取得成效充满热情，那么 Jabil 是您的不二之选。

欲更详细了解公司情况，请登录本公司网站。如果您有意应聘所述岗位，请将中英文简历及相关证书复印件选择所述方式寄至公司，并请注明相关应聘职位。来信请寄至本公司。未经录用者，简历恕不退回。谢谢！

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