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[經驗交流] 如何做一個優秀的研發QA?

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1#
發表於 2006-9-29 11:02:14 | 只看該作者 回帖獎勵 |正序瀏覽 |閱讀模式
會員中有沒有人做QA的?來討論一下,「如何做一個優秀的研發QA」!? 5 C3 x; Z; C. [- r1 z' J9 t

4 S8 @. w' n) a! z1 J聽說作這方面的,有人現在感到比較迷茫?!
分享到:  QQ好友和群QQ好友和群 QQ空間QQ空間 騰訊微博騰訊微博 騰訊朋友騰訊朋友
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5#
發表於 2011-9-22 15:37:36 | 只看該作者
职位要求:Requirements: + g- [6 L/ f8 F/ `8 c! W+ m
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 Bachelor in electronic/mechanical technical/science area; an advanced degree is preferred
( f7 o9 R- X; A* p2 ] More than 5 years in design quality management position(some years in design especially electronic medical device design is mandatory)with 5 or more years in a management position is also required. The experience on the mechanical-electronic product design is a plus ; i# S  ~3 s5 p
 Significant experience with quality systems in a Medical device environment is also required. $ M: B/ D( k6 [
 Be able to communicating with auditor(customer/TUV/internal/etc.) successfully# s( t" F1 \% M( o, D# A8 |; v
 Have up-to-date knowledge of applicable regulations, guidelines and standards(especially IEC60601-1, ISO13485, ISO9001, ISO14000, ISO16949 and FDA), knowledge on IEC60601-1 and other standard is prefered
. [8 |) Z% P' E: H9 L Independent decision-making is expected for daily work2 S% N" W+ ~& L1 G% w
 Good communication skill to communicate with different function team
. _5 X. W( v# ^" b7 l8 ~ Fluent English on communication with global team 1 u" k1 G) y: j: Z
 Profession with passion 7 O3 h2 N8 G6 U4 x
 Integrity and commitment
4#
發表於 2011-9-22 15:37:30 | 只看該作者
招聘公司:A famous IC company
0 w. a0 r; f; I7 M招聘岗位:Design Quality Manager
$ i; w% G6 a; s$ A工作地点:Shanghai
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" ~& a. i# T% a; a8 ?$ k: k岗位描述:
# Z# M1 h; T5 b! a2 E1 }/ O# HResponsibility: ) ^  h3 D9 D. p4 N' k$ t& j
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 Ensure Design organization fully compliance with regulations especially ISO9001/ISO13485/ISO16949/ISO14000 % V% y: w9 t3 D9 `. s' @3 V
 Ensure appropriate training for all personnel in-line with ISO9001/ISO13485/ISO14000/IEC60601 and associated regulatory standards and requirements for related design project and activities   @$ v8 Z/ D# R5 @. u# j
 Effective management of internal audit
8 {+ Z! ^9 W$ R  p& D Ensure effective interactions/cooperation with quality teams worldwide effectively0 _0 k6 m% d  }+ F7 l0 r/ z
 Interface/organize with regulatory agencies, customers and professional organizations for the successful audit 2 l" _4 D2 X( [; j, @  i2 z8 e
 Investigate, audit, analyze, propose, realize the improvements in quality management 8 |" m. Q. @/ @" T: |+ N* w4 m
 Schedule, prepare, organize management review meetings  Coordinate in activities relating to global quality ' P3 V; x1 e9 X0 ?' I1 l
 Provide quality management assistance and leadership to all department in design organization $ k, k% T: p" {8 j' b: \8 b' b. z
 Initiate, change and update product development process as applicable.  Performs other job-related duties as assigned.
3#
發表於 2011-9-22 15:35:25 | 只看該作者
MRB, CAR, 8D, customer complaints/RMAs, failure analysis and reporting (internal and external), and customer change notifications. Supplier management activities include: Managing supplier quality engineering in meeting product specification and process control requirements that include product and supplier qualification, audits, driving 8Ds to closure, review and approve suppliers process flows, specifications, workmanship standards, monitoring supplier performance (process CPK data, yield, test reports, qualification reports, etc.). 7 d, a6 v  {* ?, Y$ e. K

) s& ~. @$ u( jCandidate will prepare QBR and follow up on goals and objectives completed for Quality on Critical 1 suppliers, manage supplier PCN or ECN change, perform FAI (internal and outsource) to ensure critical deliverables are reviewed before engineering, pre-production and production release for Product manufacturing and to transfer process to offshore. Customer support activities include: Assisting customers in qualifying QCA as their approved supplier, completing customer questionnaires and reviewing specification, reviewing quality agreements as related to Product, packaging, Quality and Environment system, banned substances control and report results to final closure by implementing customer special requirements to include in our process. Candidate will support CQE to complete customer audits at QCA local site and suppliers’ site, perform supplier qualification of critical 1 & 2 suppliers and complete evaluation to put supplier in AVL list.6 j; k9 T  M: ~
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职位要求:
# \' y3 m( P7 z) ~- VEducation: Candidate should possess a BS or Master degree in Electrical and Electronics Engineering or equivalent Fluent in oral / written English, possess China English Test Band 6 (CET-6) Proficient in MS office software (MS-Windows, MS-Office, Outlook, etc.), Database knowledge will be an asset Experience: Minimum 5 years of direct semiconductor experience in the Quality Engineering role from multi-national companies.
2#
發表於 2011-9-22 15:35:20 | 只看該作者
招聘公司:A famous IC company
/ ?! \" `9 l! I& D  R0 C- H! S0 T招聘岗位:(Sr.) QA Engineer
! A, O' B% l% W+ Z' z; ~1 e  b8 l工作地点:Shanghai
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岗位描述:
3 k2 h  Y. W, R- _9 `& Q" kDescription of Function & Responsibility The (Sr.) QA Engineer will report to the QA Manager in Qualcomm xx Shanghai Design Center (SDC) The candidate will be responsible for supporting QCA QMS and EMS (quality and environment management system) for SDC, head office and other sites if needed. A positive attitude towards teamwork is required as this candidate will work closely with functional groups and subcontractors to coordinate the introduction of new products and ensure product manufacturability and quality with high yields and zero defects in outgoing shipments. 6 m: ^/ _0 P/ d2 ]' c0 M
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Specific activities include: SDC Quality System Construction Candidate will be a key staff to coordinate SDC ISO 9001 system certification / maintenance Candidate may support head office and other sites ISO 9001 certification / maintenance if needed Coordinator of routine internal quality audit Product Quality Assurance: Review technical problems from our products and processes, recommending solutions, managing product and process nonconformance:
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