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Principal Reliability Engineer
Billerica, Massachusetts, United States of America
·
On-site
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Full-time
·
3w ago
We anticipate the application window for this opening will close on - 28 May 2026
Position Description:
Principal Reliability Engineer for Medtronic, Inc located in Billerica, MA. Responsible for providing quality engineering support to ensure the successful development of Medtronic medical products. Ensure design control requirements are met and products are developed and manufactured in accordance with applicable industry standards, regulatory requirements and customer requirements. Update risk mgmt. documents to reflect updated or changed controls and mitigations, compliance evidence for standards, and risk estimates in response to post-market surveillance. Utilize Mechanical Geometric Dimensioning and Tolerancing (GD&T) and Root Cause Analysis (RCA). Navigate the complexities of government and industry regulations to include FDA 21 CFR Part 820, Current Good Manufacturing Practices (cGMP), ISO 14791, ISO 13485, ISO 9001, ISO 10012, and ISO 17025. Support various regulatory audits for Quality system process documents and records. Coordinate various Corrective & Preventive Actions (CAPA) programs as well as Lean Six Sigma, Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP). Utilize risk analysis including Failure Mode Effect Analysis (FMEA), verification and validation (V&V), methodical problem solving, product design, and manufacturing engineering. Leverage Design of Experiments (DOE) and Statistical Analysis. Execute and utilize development protocols to include Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Test Method Validations (TMV). Responsible for Capital equipment and single-use device design quality and design controls. #.
The position will be onsite at the Billerica, MA location 4 days per week. Up to 25% domestic and international travel to various Medtronic project sites in Minneapolis, Minnesota; Boston, MA; Montreal, Canada; and Galway, Ireland. Reason: Project planning, support, and training
Basic Qualifications:
Master’s degree in Mechanical or Biomedical Engineering or related engineering field and five (5) years of experience as a quality or manufacturing engineer or related engineering field. Experience must include a min. of five (5) years of each of the following: Mechanical GD&T and RCA; FDA 21 CFR Part 820, ISO 14971, ISO 13485, ISO 9001, ISO 10012, and ISO 17025; Supporting regulatory audits for Quality system process documents and records; Lean Six Sigma, GMP, GDP, and CAPA; Risk analysis, FMEA, V&V, methodical problem solving, product design, manufacturing engineering; DOE and statistical analysis; IQ/OQ/PQ, and TMV; Capital equipment and single-use device design quality and design controls. Up to 25% domestic and international travel to various Medtronic project sites in Minneapolis, Minnesota; Boston, MA; Montreal, Canada; and Galway, Ireland.Reason: Project planning, support, and training.
The position will be onsite at the Billerica, MA location 4 days per week.
Salary: $149,500 to $187,200 per year
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
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Medtronicについて

Medtronic
PublicMedtronic plc is an American-Irish medical device company. The company's legal and executive headquarters are in Ireland, while its operational headquarters are in Minneapolis, Minnesota. Medtronic rebased to Ireland following its acquisition of Irish-based Covidien in 2015.
10,001+
従業員数
Minneapolis
本社所在地
$100B
企業価値
レビュー
3.9
10件のレビュー
ワークライフバランス
3.2
報酬
4.0
企業文化
4.1
キャリア
3.4
経営陣
3.8
72%
友人に勧める
良い点
Supportive management
Great team culture and collaborative environment
Professional growth and development opportunities
改善点
Heavy workload and high pressure
Long working hours and high expectations
Fast-paced and stressful environment
給与レンジ
1,149件のデータ
Junior/L3
Junior/L3 · Advanced Analytics Analyst
3件のレポート
$95,911
年収総額
基本給
$73,778
ストック
-
ボーナス
-
$66,383
$95,911
面接体験
11件の面接
難易度
3.4
/ 5
期間
14-28週間
体験
ポジティブ 0%
普通 55%
ネガティブ 45%
面接プロセス
1
Application Review
2
Recruiter Screen
3
Technical Phone Screen
4
Onsite/Virtual Interviews
5
Panel Interview
6
Offer
よくある質問
Technical Knowledge
Coding/Algorithm
Behavioral/STAR
Past Experience
System Design
ニュース&話題
Oak Harvest Investment Services Grows Holdings in Medtronic PLC $MDT - MarketBeat
MarketBeat
News
·
1d ago
Medtronic PLC (NYSE:MDT) Receives Consensus Recommendation of "Moderate Buy" from Brokerages - MarketBeat
MarketBeat
News
·
2d ago
KBC Group NV Acquires 21,384 Shares of Medtronic PLC $MDT - MarketBeat
MarketBeat
News
·
2d ago
Is Medtronic a Better Buy Than Abbott Laboratories? - Trefis
Trefis
News
·
2d ago