Sr. Manufacturing Engineer (Fraser, MI) jobs in United States
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Getinge · 12 hours ago

Sr. Manufacturing Engineer (Fraser, MI)

Getinge is a company dedicated to making life-saving technology accessible for more people. They are seeking a Senior Manufacturing Engineer who will oversee engineering activities, develop manufacturing processes, and drive continuous improvement efforts in quality and cost savings.

BiotechnologyHealth CareLife ScienceMedicalMedical Device
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H1B Sponsor Likelynote

Responsibilities

Responsible for engineering projects, incorporating newest manufacturing technologies & methods, resolving engineering problems, and improving existing manufacturing processes/equipment
Responsible for upstream equipment qualification deliverables (URS, FAT, SAT, etc.)
Prioritize and communicate project priorities based on current business needs
Responsible for achieving product quality, productivity, and standard cost goals
Maintain compliance with all regulatory standards for product and personnel safety
Guide, direct, and coordinate facility moves, process transfers, and new equipment installations ensuring improved product quality, manufacturing efficiencies, production yields, and reduce product costs
Support nonconformance investigation
Responsible for identification and communication with external machine builders and systems integrators
Support manufacturing objectives as specified by the management team by promoting investigation, inventiveness, creativity and solutions to various process, implementation, and material flow/control problems
Communicate new ideas, technology advances, and opportunities to management team for review, evaluation and action
Responsible for developing and maintaining department expense and capital budget(s)
Create and maintain a safe environment. Ensure legal requirements and safety policies are enforced
Assist in special projects as needed
Contributes to team effort by accomplishing related duties as requested

Qualification

Manufacturing process developmentMedical device industry experienceProject managementRegulatory compliance knowledgeCollaboration skillsComputer skillsHighly organizedNegotiation skillsSelf-motivated

Required

Bachelor's degree in Engineering, Industrial Management, or related field or equivalent
Minimum 10 years of experience within a manufacturing or process development environment, preferably within the Medical Device Industry
Ability to work with flexible and changing production schedules
Must be able to collaborate effectively with others, and work well within cross-functional teams and across multiple sites, as applicable
Self-motivated and have the ability to manage projects and problem solve on a regular basis
Highly organized with strong project management and technical abilities
Demonstrated ability to develop strategies that will help build a positive manufacturing environment
Ability to communicate with machine builders and system integrators
Strong negotiation skills required
Strong computer skills, including MS Office applications (Word/Excel) are required
Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function)
Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function)
Attend all required Quality & Compliance training at the specified interval
Adopt the 'Beyond Compliance Quality Culture' in the work environment; always meet and exceed requirements

Benefits

Health, Dental, and Vision insurance benefits
401k plan with company match
Paid Time Off
Wellness initiative & Health Assistance Resources
Life Insurance
Short and Long Term Disability Benefits
Health and Dependent Care Flexible Spending Accounts
Commuter Benefits
Parental and Caregiver Leave
Tuition Reimbursement

Company

Getinge identifies customer issues and promotes clinical and economic benefits and follow and support the customer decision process.

H1B Sponsorship

Getinge has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2024 (3)
2023 (2)
2022 (2)
2021 (2)
2020 (5)

Funding

Current Stage
Public Company
Total Funding
$539.31M
2017-10-19Post Ipo Equity· $539.31M
2002-06-28IPO

Leadership Team

C
Christoffer Å.
Chief Information Security Officer
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Joanna Engelke
EVP Quality Compliance, Regulatory, Medical
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Company data provided by crunchbase