Corza Medical logo

Manufacturing Engineer, Ophthalmology, (Must Reside in Michigan)

Corza Medical

Grand Blanc, MIFull-time$75–85K/yrTracked 3w agoSeen in employer's feed 5 days ago

Most applications go out cold — see where you stand first. No sign-up to start.

At a glance

Compensation
$75–85K/yr
Location
Grand Blanc, MI
Schedule
Full-time
Work Authorization
US work authorization required

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Corza Medical is hiring a Manufacturing Engineer, Ophthalmology, (Must Reside in Michigan). Corza Medical seeks a Manufacturing Engineer to lead safety, quality, delivery, and operational efficiency initiatives within its ophthalmology medical device manufacturing facility in Grand Blanc, Michigan. The role involves designing, implementing, and reviewing manufacturing procedures and equipment, improving labor efficiency, reducing costs, and ensuring compliance with FDA and ISO standards while supporting cross‑functional projects and documentation.

Key focus areas include Design, implement, and review manufacturing procedures and equipment., Research controls and automation techniques, test new systems for efficiency, and plan factory layouts to optimize production., and Lead cross‑functional projects to improve labor efficiency and optimize product quality..

Successful candidates bring 2-4 Years Direct Engineering Support Of Quality Management Systems, Bachelor's In Engineering Discipline, and Authorized To Work For Any Employer In The US. Important skills include Designing Manufacturing Procedures, Implementing Manufacturing Procedures, Reviewing Manufacturing Procedures, Designing Manufacturing Equipment, Implementing Manufacturing Equipment, and Reviewing Manufacturing Equipment. Preferred (not required): AutoCAD.

Skills & qualifications

RequiredNice to have

Skills

Designing Manufacturing ProceduresImplementing Manufacturing ProceduresReviewing Manufacturing ProceduresDesigning Manufacturing EquipmentImplementing Manufacturing EquipmentReviewing Manufacturing EquipmentResearching Controls and Automation TechniquesTesting New Systems for EfficiencyPlanning Factory LayoutsOptimizing ProductionLabor Efficiency ImprovementProduct Quality OptimizationQualifying Replacement ComponentsReducing Manufacturing Operating CostsContinuous Improvement Kaizen ActivitiesRoot Cause AnalysisProblem SolvingResolving Mechanical ProblemsImplementing Effective SolutionsRisk Management Reports & AssessmentsEnvironmental and Health CompliancePersonnel Safety ActivitiesSite and Contractor-Based Maintenance ProgramMaterial Review Board ActivitiesContinuous Improvement InitiativesMedical Device Design and DevelopmentCompilation of Device Design History FilesDesign VerificationDesign ValidationInternal Quality System Programs ComplianceManagement ReviewEmployee TrainingCorrective and Preventive ActionsInternal Quality AuditsGenerating Engineering DrawingsMaintaining Engineering DrawingsGenerating LabelingMaintaining LabelingGenerating IFUsMaintaining IFUsGenerating Work InstructionsMaintaining Work InstructionsFDA Quality System Regulation (21 CFR 820)ISO 13485-2016Process EngineeringProcess ValidationTest Method DevelopmentOrganizational SkillsRecord Keeping SkillsCommunicationMicrosoft WordExcelPowerPointSolidWorksLabelviewAutoCADFDA Quality System Regulation (21 CFR 820) KnowledgeISO 13485-2016 KnowledgeProcess Engineering Validation Test Method DevelopmentControls and Automation ExperienceContinuous Improvement KaizenRisk Management Reports and AssessmentsExcellent Organizational and Record KeepingClear Communication Skills

Qualifications

Bachelor's Degree in Engineering Discipline2-4 Years Experience in Direct Engineering Support of Quality Management SystemsMust Reside in MichiganAuthorized to Work for Any Employer in the USLean Six Sigma Certification

Benefits

Medical Insurance
Paid Time Off
401(k) Match

Full job description

Manufacturing Engineer, Ophthalmology, (Must Reside in Michigan)

Location of Work Grand Blanc, MI

Employment Type Full Time Employee

Job Description

Our mission

At Corza Medical, our mission is to champion surgical providers with remarkable service and exceptional products that save time, money, and effort. We are a passionate team guided by our core belief that you should never have to choose between performance, value, and a quality customer experience. We are here to support you every step of the way.

Our brand promise

We deliver a collaborative experience by working directly with the surgical community to ensure you get the exact surgical tools you need at the right time and the right price.

  • Remarkable service: A seamless, personal process designed around you and your needs.

  • Trusted performance: Our product family is the result of years of experience championing surgeons and listening to their expertise.

  • Outstanding value: No matter the surgical specialty, we deliver quality products for all markets.

Our people promise

Excellence is our Specialty and what makes us successful is our people. We are committed to fostering a positive, empowering and growth-oriented environment where all team members are encouraged to share their opinions and ideas. That means you will work alongside an accomplished and highly collaborative team that inspires commitment to our goal in attaining excellence in everything they do.

Job Purpose Summary

We are seeking a Manufacturing Engineer with an engaging and generous spirit who excels in a dynamic, growth-oriented environment to join our team. The candidate will lead aspects pertaining to safety, quality / customer satisfaction, delivery, and operational efficiency within a medical device manufacturing facility.

What you will do

  • Responsible for designing, implementing, and reviewing the procedures and equipment involved in the manufacturing process. Their duties include researching controls and automation techniques, testing new systems for efficiency and planning factory layouts to optimize production.

  • Lead cross functional projects to improve labor efficiency, optimize product Quality, qualify replacement components, and reduce Manufacturing operating costs through Continuous Improvement Kaizen activities.

  • Be adept in resolving and determining root cause of mechanical problems encountered in Production during the Assembly and Testing of products and capable of timely implementing effective solutions.

  • Support ongoing development and maintenance of Risk Management Reports & Assessments.

  • Major contributor within site Environmental and Health compliance and personnel Safety activities.

  • Lead site and contractor-based maintenance program (preventive and corrective).

  • Assist in Material Review Board activities ensuring proper trending, closure of issues and dispositions are appropriately addressed. Drive continuous improvement initiatives based on MRB data.

  • Support manufacturing aspects of design and development of medical devices including compilation, review, and approval of device design history files, risk management reports, coordinate design verification/design validation.

  • Support ongoing compliance of internal quality system programs including:

  • Management Review

  • Employee Training

  • Corrective and Preventive Actions

  • Internal quality audits

  • Support the generation of and maintain documents including; engineering drawings, labeling, IFUs, Work Instructions, etc.

  • Other duties as assigned.

What you will need

  • Minimum of 2-4 years’ experience in direct engineering support of quality management systems for medical device & biologics development and manufacturing of sterile devices, (US & EU) class I, II devices and tissue products.

  • Solid working knowledge of FDA Quality System Regulation (21 CFR 820) and ISO 13485-2016.

  • Bachelor’s degree in an engineering discipline.

  • Experience in process engineering/validation/test method development.

  • Excellent organizational and record keeping skills.

  • Ability to clearly communicate information/ideas/recommendations (verbally and in writing) with technical, administrative and management personnel.

  • Moderate controls and automation experience.

  • Proficiency in information technology applications such as MS Word, Excel, and PowerPoint.

  • Proficiency in SolidWorks and Labelview.

  • AutoCAD system a plus.

  • Root cause analysis and problem-solving skills. Lean / Six Sigma certification is a plus.

  • In order to qualify for this position, applicants must be authorized to work for ANY employer in the US. We are unable to sponsor or take over sponsorship of employment Visa at this time.

What we value

  • Customer First - We deliver extraordinary experiences.

  • Accountability - We do what we say.

  • Integrity - We do what is right.

  • Inspired - We love what we do.

  • One Global Team -We before me, always.

Join us today and Excel@Corza !

Corza Medical offers a competitive benefits package including medical, 401K, vacation and sick time, paternal leave and other benefits.

A reasonable estimate of the current pay range for this role is $75,000 - $85,000/annual. Further, pay is offered based on geographic location, internal equity, market data, applicant’s job-related skills, commensurate experience, required licensures, certifications, and certain degrees.

Corza Medical is an equal opportunity employer. Corza Medical evaluates qualified applicants without regard to race, color, marital status, religion, sex, sexual orientation, gender identity, age, national origin, physical or mental disability, veteran status or other protected characteristics.

Notice To Third Party Agencies:

Corza does not accept unsolicited resumes from recruiters, employment agencies, or other staffing services. Any unsolicited resumes, including those submitted to hiring managers or other business leaders, will become the property of Corza Medical and Corza Medical will have the right to hire that candidate without reservation – no fee or other compensation will be owed or paid to the recruiter, employment agency, or other staffing service.

You've read the whole posting — now see how you match it.