Associate Engineer (Medical device Testing/Validation) jobs in United States
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Aequor · 1 day ago

Associate Engineer (Medical device Testing/Validation)

Aequor is seeking an Associate Engineer to support medical device testing and validation. The role involves performing standardized tests, analyzing data, and collaborating with engineers to improve designs and testing methods.

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H1B Sponsor Likelynote
Hiring Manager
Shubham Chand
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Responsibilities

Ability to perform standardized tests per SOP and test methods
Understands protocols, data collection, and proper use of lab equipment
Focused on accuracy, repeatability, and compliance
Perform equipment validation (IQ/OQ, etc.)
Capable of analyzing test results, identifying trends or failures, and summarizing findings clearly
Writes structured test protocol, reports and maintains documentation aligned with quality and regulatory requirements
Can identify potential issues in performance and support investigations (e.g., basic CAPA input, troubleshooting test failures)
Collaborates with engineers to improve designs, performance or test methods based on results
Supports in the designs and development of a wide variety of packaging and/or device used for the protection, display, handling, and delivery of ophthalmic pharma products
Performs assigned tasks under general supervision in support of approved projects
Executes engineering studies, conduct testing and data analysis under direction of senior OH team members. Receives technical guidance from senior OH staff on the design of experiments
Applies general technical skills to complete assigned work and solves routine problems of limited scope
Thoroughly and clearly documents experiments in laboratory notebook and assists in preparation of technical documents
Drafts protocol and reports to document related activities
Drafts and routes standard operating procedures as required
Drives effective actions for compliance within the agreed timelines
Ensures continual quality system compliance by adherence to established and evolving QS requirements
Communicates and collaborates with colleagues and with supervisor
General use, set-up and upkeep of laboratory, including equipment/instrumentation
Familiarity with statistical analysis and software is preferred

Qualification

Technical Testing CompetencyData AnalysisProblem SolvingEquipment ValidationMedical Device ExperienceStatistical AnalysisDocumentation SkillsCollaborationCommunication

Required

Hands-on and Technical Testing Competency
Ability to perform standardized tests per SOP and test methods
Understands protocols, data collection, and proper use of lab equipment
Focused on accuracy, repeatability, and compliance
Perform equipment validation (IQ/OQ, etc.)
Capable of analyzing test results, identifying trends or failures, and summarizing findings clearly
Writes structured test protocol, reports and maintains documentation aligned with quality and regulatory requirements
Can identify potential issues in performance and support investigations (e.g., basic CAPA input, troubleshooting test failures)
Collaborates with engineers to improve designs, performance or test methods based on results
Supports in the designs and development of a wide variety of packaging and/or device used for the protection, display, handling, and delivery of ophthalmic pharma products
Performs assigned tasks under general supervision in support of approved projects
Executes engineering studies, conduct testing and data analysis under direction of senior OH team members
Receives technical guidance from senior OH staff on the design of experiments
Applies general technical skills to complete assigned work and solves routine problems of limited scope
Thoroughly and clearly documents experiments in laboratory notebook and assists in preparation of technical documents
Drafts protocol and reports to document related activities
Drafts and routes standard operating procedures as required
Drives effective actions for compliance within the agreed timelines
Ensures continual quality system compliance by adherence to established and evolving QS requirements
Communicates and collaborates with colleagues and with supervisor
General use, set-up and upkeep of laboratory, including equipment/instrumentation
Bachelor's Degree or Equivalent + 4 years of directly related experience (or high school +8 yrs; Assoc.+6yrs; M.S.+0 yrs)
The ability fluently read, write and communicate in English
Work efficiently and productively with other team members and external partners
Adheres to Alcon's guidelines for appropriate workplace behaviors and attitudes

Preferred

Prior experience working with Alcon is strongly preferred
Experience in medical device is preferred
Familiarity with statistical analysis and software is preferred

Company

Aequor

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Since 1998, Aequor has provided exceptional workforce staffing services in multiple industries.

H1B Sponsorship

Aequor 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 (2)
2024 (2)
2023 (1)
2022 (3)
2021 (1)
2020 (5)

Funding

Current Stage
Growth Stage

Leadership Team

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Kamalpreet S. Virdi
CEO & Chairman
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Company data provided by crunchbase