採用
Work Flexibility: Hybrid or Onsite
What will you do:
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Primarily responsible for Risk management and risk assessment as per ISO 14971, Risk Table creation & Analysis, FMEAs, Quality Plan, Literature Review, Device Master Record, Quality Training Plan and Technical File.
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Primary participant in new supplier selection, validation, and contract development. Assists vendors in resolving manufacturing and quality issues as required.
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Partners with the operations team to develop and maintain a robust internal and external supply chain.
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Develop procedures for incoming, in-process and final inspections for new product development
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Assists/Leads in the trending and analysis of quality data (e.g. complaints, scrap, warranty return rate, etc.) and provides guidance to address issues as appropriate.
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Authors and reviews procedures to ensure GMP and ISO 13485 compliance and provide inputs for NPDP for adherence to QMS along with good documentation practices
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Lead product quality related projects. Supports the business in addressing and solving quality problems
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Support process validation programs for new product development
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Work with engineering & manufacturing teams to develop robust verification test strategies to ensure product safety and reliability
What you need:
Basic Qualifications:
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Bachelors in mechanical or biomedical or Biotech Engineering.
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Good understanding of Quality Management Systems. (ISO 13485, 21 CRF 820)
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Minimum 2 to 6 years of relevant work experience.
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Experience in the NPD process and various phases of new product development.
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Knowledge of ISO 14971, IEC 62366, 60601-1 family of standards.
Preferred Qualifications:
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Good analytical and problem-solving skills.
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Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams.
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Expert-level knowledge of current industry standards for New Product Development and risk management practices
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Excellent communication and presentation skills
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Must have delivered multiple projects in AQE function and understand Risk Management processes in depth.
Travel Percentage: 20%
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0
応募クリック数
0
模擬応募者数
0
スクラップ
0
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Strykerについて

Stryker
PublicStryker Corporation is an American multinational medical technologies corporation based in Kalamazoo, Michigan.
10,001+
従業員数
Kalamazoo
本社所在地
$75B
企業価値
レビュー
2.9
2件のレビュー
ワークライフバランス
3.0
報酬
2.5
企業文化
2.5
キャリア
2.8
経営陣
2.0
35%
友人に勧める
良い点
Well-known company in medical field
Potential for career growth
Opportunity to build teams
改善点
Low compensation
Poor management practices
Unfulfilled promotion promises
給与レンジ
2,009件のデータ
Senior/L5
Senior/L5 · Senior Portfolio Manager
1件のレポート
$173,157
年収総額
基本給
$150,571
ストック
-
ボーナス
-
$173,157
$173,157
面接体験
4件の面接
難易度
2.8
/ 5
期間
14-28週間
体験
ポジティブ 0%
普通 50%
ネガティブ 50%
面接プロセス
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Gallup Assessment
5
Field Experience/Ride Along
6
Final Presentation
よくある質問
Behavioral/STAR
Sales Experience
Culture Fit
Past Experience
Situational Judgment
ニュース&話題
Stryker Corporation (NYSE:SYK) Given Consensus Rating of "Moderate Buy" by Brokerages - MarketBeat
MarketBeat
News
·
4d ago
Stryker Sports Medicine Associate
Hello, I am interested in applying for a Stryker Sports medicine associate position, and was wondering if anyone would recommend the role? I just want to make sure this lines up with my goals and desires before I go into an interview and waste someone’s time. I would love to hear some people’s experiences who worked in this specialty, and the biggest worries I have is career trajectory and work/life balance. I've worked in Logistics and in SaaS so it'll be another industry change for me.
·
5d ago
·
2
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3
Stryker Hack Affects First Quarter Results - BankInfoSecurity
BankInfoSecurity
News
·
5d ago
Stryker leads West Michigan public companies with $25.1B in revenue - Crain's Grand Rapids
Crain's Grand Rapids
News
·
6d ago