職種
業種
勤務地
掲載日
キーワード
  単語を含む 全て含む
 
職種
専攻 住所
職務経験 性別
月給
キーワード
  単語を含む 全て含む
 
Resume data : Code 0001571 Last update : 13 ต.ค. 2557
名 : xxxxxxxxxx 姓 : xxxxxxxxxx
現住所 : xxxxxxxxxx
E-mail : xxxxxxxxxx
電話番号 : xxxxxxxxxx
プロフィール
  生年月日 3 พ.ค. 2514
性別 หญิง
未婚・既婚 โสด
身長 156 cm.
体重 75 kg.
国籍 Thai
宗教 Buddhist
兵役義務あり／なし
応募用件
  応募職ポジション
1. Auditor
2. QA
3. RD
希望月給 40,000
勤務地
学歴
卒業年 2003 大学名 Chulalongkorn University
レベル Master’s degree
Qualification วิทยาศาสตรมหาบัญฑิต
Subject Petro chemistry and Polymer science
GPA 3.10
卒業年 1995 大学名 Chiang Mai Rajabhat Institute
レベル Bachelor’s degree
Qualification วิทยาศาสตรบัญฑิต
Subject Applied Biology
GPA 3.10
職務経歴
過去の職務年数 0 Year
まで勤務 October 2006
 まで勤務 Present 		会社名 TOP Cosmetic and manufacture Co.; Ltd
現住所 - 122/1 หมู่ 5 พุทธมณฑล สาย 5 กระทุ่มแบน อ้อมน้อย สมุทรสาคร
最後の月給 50000
職位 QA&MR Manager
Duty - Work
Quality Assurance function in Cosmetic Product. • Take final responsibility for product quality assurance within the manufacturing process starting from raw material verification to finished goods acceptance for the site in order to fulfill customer requirements. • Translate the corporate quality strategy into concrete projects and implement these projects in order to ensure quality within the site meets the international standards. • Define the guidelines / procedure in handling issues, non-conformities and non-conformances within the site in order to make sure that problem re acted upon in timely manner and prevent recurrence. • Manage, monitor, evaluate and coordinate Management System of the site in order to ensure compliance with international standards in order to have and effective and efficient operation of the established Management System. • Manage the document control within the entire organization in order to ensure conformance with the requirements defined in the Management System. • Qualify potential raw and auxiliary material suppliers in coordination with Purchasing in order to ensure that purchased products satisfy the site and customer requirements. • Coordinate, coach, identify training needs and growth paths and draw up a planning for a team of employees charged with the execution and implementation of the quality guidelines and control in order to ensure a well-functioning team. • Act as point of contact for the key customers concerning quality matters and be a potential interlocutor for issues belonging to his/ her competencies in order to guarantee customer satisfaction. • Provide leadership, consultation and advice to all departments on technical issues to support the achievement of quality, product safety and production goals. • Supports Marketing, Business Developments and Production team for research new products, development existing products and process. • Responsible for reporting the potential or the risk that might impact the safety of workers or working environment or safety management systems to upper ordinates or identified persons. • Any activities related to company business assigned by Director and Managing Director.
まで勤務 November 1996
  まで勤務 September 2005		 会社名 Pfizer (Thailand) Ltd
現住所 - 415 สุขุมวิท 74 สำโรงเหนือ สมุทรปราการ
最後の月給 38000
職位 QA Supervisor
Duty - Work
1. Carried out Incoming material quality assurance, Lab testing & trouble shooting in • accordance with the Pfizer Master Specification. * Chemical and microbiological tested of Raw materials more than 250 kinds before used in process. * Chemical and microbiological tested during mixed the in process Finishing supplies were checked before used in the Packing Line * Validation and weekly checked DI water before used in process ensured that the DI water weren’t have microorganism and chemical out of the Pfizer specification or USP 23 Remark The entire test above had to use the test method of Pfizer master specification, USP, BP, Food chemical codex, Waste water treatment and SOPs. 2. Cleaning validation must only used for the new production line and due date to commit in SOPs or compliance. * Pfizer standard requirements and FDA had to tested the air sampling (tested hydrocarbon and microorganism in the production line for controlled the environment. 3. Coordinated with another departments and suppliers when the tested results had the problems (out of specification, out of trend) to solving the problems with production team. 4. Purchasing and controlling all equipments and chemicals to use in QA department. 5. New equipments had to performed qualification (IQ, OQ and PQ) before used. 6. Performing and Reviewing the SOPs to use in Laboratory and tested method such as Sanitation Evaluation, Sampling method of raw material, Monitoring of Compressed Air, Ion Chromatograph, Chemical hazard communication, Lab Safety Manual, HPLC, GC, UV and Another ฯ. • 7. Cooperating with Production Team and Marketing Team in order to investigate causes of customer complaints by supporting tested results
まで勤務
  まで勤務 		会社名
現住所 -
最後の月給
職位
Duty - Work
研修
まで勤務 March 2012
まで勤務 March 2012		 研修機関名 วิทยากรภายนอก อาคารว่องวานิช
研修コース名 KaiZen
まで勤務 May 2010
まで勤務 May 2010		 研修機関名 Technology Promotion Association (Thailand-Japan)
研修コース名 Training QCC Control
まで勤務 June 2005
まで勤務 June 2005		 研修機関名 Moody International (Thailand) Ltd.
研修コース名 Training ISO 9000:2001 Lead Auditors,
Ability and performance
  言語能力
言語 ไทย 会話 ดี 読み ดี 書き ดี
言語 อังกฤษ 会話 ดี 読み ดี 書き ดี
タイ語 30 wpm.
英語 20 wpm.
運転免許の有無 車
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その他の能力

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レファレンス
อาจารย์ จิตนา สายวรรณ




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