Responsibilities:
1. Validation uation for new or modified process/equipment system/facility.
a) Process characterization study.
b) Identify key process variables that would affect product quality.
c) Identify equipment critical part/feature that would affect process parameter and product quality.
d) Hazard Analysis/risk assessment and other process study.
e) Develop VMP for whole processes of production by product with necessary justifications based on above assessment/study.
2. Design and develop validation protocol.
a) Design validation study features, such as sampling, testing, or analytical methodologies.
b) Direct validation activities, such as protocol creation or testing.
c) Prepare validation protocols for new or modified manufacturing processes, systems, or equipment for medical, electronics, or other types of production.
d) Study product characteristics or customer requirements to determine validation ives and standards.
3. Conduct validation or qualification tests based on internal protocols and/or external standards.
a) Assist in training operators or other staff on validation protocols.
b) Analyze validation test data to determine whether systems or processes have met validation criteria or to identify root causes of production problems.
c) Coordinate the implementation or scheduling of validation testing with affected departments and personnel.
d) Identify deviations from established product or process standards and provide recommendations for resolving deviations.
e) Manage deviations and changes in order to guarantee that these are well documented and corrective s are taken and followed-up upon.
f) Draw samples of raw materials, or intermediate and finished products for validation testing.
g) Conduct audits of validation or performance qualification processes to ensure compliance with internal or regulatory requirements.
h) Procure or devise automated validation test stations or other test fixtures and equipment.
i) Align facility validation strategies and policies with actual outcomes
4. Continuous competence development in Validation and maintenance of validation documentation and database.
a) Communicate with regulatory agencies regarding compliance documentation or validation results.
b) Participate in internal or external training programs to maintain knowledge of validation principles, industry trends, or technologies.
c) Prepare, maintain, or review validation and compliance documentation.
d) Create, populate, or maintain databases for tracking validation activities, test results, or validated systems.
5. Deal with other assignments assigned by superior.

Qualification:
1. College degree or above, major in electronics, electromechanical or equivalent.
2. Above 5 years relative work experience, QA experience is a plus.
3. Good command of written English.
4. proactive, responsible, independent.

公司简介
秋时电子（深圳）有限公司成立于1996年12月20日，拥有过硬的工程技术和生产管理经验，专门为客户提供复杂工艺产品和精密度高的产品。公司在香港和美国分别设有办事处。

公司的主要产品有光学仪器、全自动电子美容器、电子/医用传感器、瞄准器、透镜、工业控制器、信号计数器以及PCBA等。产品100%外销欧洲以及北美，公司以高效的服务、卓越的品质深得客户信赖，已经取得BSI ISO9001：2008及 BSI ISO13485：2003的认证。
　　
发展目标
1. 成为欧洲以及北美客户在中国地区首选制造商。
2. 成为低成本、高品质的一流制造商。
3. 成为使员工最有成就感和归属感的优秀企业。

薪资与福利
1. 公司提供富有竞争力的薪酬。
2. 公司实行5天8小时工作制度。
3. 按国家规定提供社会保险及住房公积金。
4. 每年7天有薪年假，且享受年终双薪。
5. 公司为每位员工提供餐补及安全舒适的住宿(或房补)。
6. 公司设有种类众多的奖项：优秀员工、终身荣誉奖、杰出贡献奖等。
7. 其他福利：部门娱乐活动经费、生日礼金、结婚礼金、生育礼金、节日礼品或礼金、丧葬慰问金、出差补贴、年终聚餐及抽奖、员工专业技能培训、学历教育、户口招调等。

联系我们
公司地址：深圳市南山区西丽白芒南岗第一工业区8栋
乘车路线：市内方向乘392、332、316、326、325于“白芒关”站台下车，往出关方向前行100米；石岩乘392、332、316、326、325于“南岗工业区”站台下车。

　
热诚欢迎您加盟秋时电子，成为秋时精英的一员。
　　

Quasar electronics （SZ）co.， Ltd was established in Shenzhen, China in 1996, giving us time to build a strong Management System. Engineering Support and Project Management functions are geared towards meeting international customer requirements, giving customers serious communication & clear cooperation. We has offices in Hong Kong and the United States.

Quasar excels in manufacturing complex and/or precision products, which require consistent quality & yields; High Precision Assembly, such as optics, sensors (medical/industrial), and products assembled under a microscope. Complex products may involve many different types of parts/components assemblies: SMT, Thru-hole & COB, metal, plastic, and silicone-rubber, among others. Alternatively, different types of assembly methods: swaging, ultrasonic welding, calibration, testing, clean room, & consumer packing

Quasar is ISO9001 and ISO 13485 Certified, by BSI, since 1998, initially ISO9002 and in 2002 updated to the present ISO certification.

Quasar manufactures products for the Medical (about 30-40%), Consumer, Telecommunication and Agricultural Markets, among others.