Device Engineer #26-12079

US Tech Solutions, Inc.

Thousand Oaks, CA

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JOB DETAILS

SALARY

$42–$45.70 Per Hour

SKILLS

Analysis Skills, Artificial Intelligence (AI), Audio Engineering, Bioengineering, Biomedical Engineering, Biotech and Pharmaceutical, Change Control, Clinical Laboratory, Communication Skills, Continuous Improvement, Cross-Functional, Data Analysis, Data Management, Data Visualization Tools, Delivery Management, Design Verification, Detail Oriented, Document Management, Documentation, Drug Delivery Devices, Follow Through, GMP (Good Manufacturing Practices), High School Diploma, ISO (International Organization for Standardization), Identify Issues, Laboratory, Laboratory Notebook, Laboratory Testing, Management Strategy, Manufacturing Analysis, Manufacturing Operations, Mechanical Engineering, Mechanical Testing, Medical Equipment, Minitab, Multitasking, Operational Communications, Operational Support, Organizational Skills, Presentation/Verbal Skills, Product Design, Product Development, Product Documentation, Product Lifecycle, Product Support, Product Testing, Product/Service Launch, Productivity Management, Project Execution, Project Tracking, Project/Program Coordination, Protocol Analysis, Quality Assurance Methodology, Quality Management, Record Keeping, Regulations, Reliability Testing, Risk Analysis, Risk Management, Root Cause Analysis, Scientific Principles, Statistics, Team Player, Technical Analysis, Technical Operations, Technical Presentation, Technical Support, Technical Writing, Test Design, Test Lab, Test Plan/Schedule, Test Requirements, Test Strategy, Testing, Traceability, Validation Testing, Writing Skills

LOCATION

Thousand Oaks, CA

POSTED

14 days ago

Duration: 12 months contract

Job Description:

The Device Engineer will support the design, development, and lifecycle management of commercialized drug delivery devices within a regulated design control environment. This role combines hands-on laboratory execution with technical operations support and sustaining engineering activities for combination products from development through global launch.
The engineer will support mechanical drug delivery devices, including prefilled syringes, through laboratory testing, design verification support, failure investigations, design change assessments, and maintenance of Design History File (DHF) documentation and traceability records. A key aspect of the role is understanding how testing activities support user needs, product requirements, risk controls, and verification strategies within the design control process.
This position requires a candidate who is comfortable working directly in the laboratory while applying structured engineering and documentation practices in a regulated environment. The engineer will collaborate cross-functionally with scientists, engineers, quality, manufacturing, and operations partners to support product improvements, technical investigations, inspection readiness activities, and execution of key project deliverables.
The successful candidate will demonstrate strong technical judgment, attention to detail, and the ability to connect day-to-day execution with broader product quality, compliance, and development objectives.

Ideal Candidate:

The ideal candidate is a hands-on engineer with experience executing laboratory testing, troubleshooting technical issues, and working within regulated product development environments. They are detail-oriented, organized, and capable of producing high-quality technical documentation and reliable experimental results.
They understand how laboratory activities support broader design control objectives, including traceability, risk management, verification strategies, and product quality. This person is able to connect user needs, product requirements, and test outcomes within a structured development process.
The ideal candidate demonstrates strong ownership, sound engineering judgment, and effective collaboration skills. They are comfortable managing multiple priorities in a fast-paced environment and are proactive in using digital tools such as Smartsheet, electronic lab notebooks, data visualization tools, and AI-enabled productivity tools to improve coordination, workflow efficiency, documentation quality, and team communication.

Key Responsibilities:

Support the design, development, and lifecycle management of commercialized drug delivery devices within a regulated design control environment.
Contribute to sustaining engineering activities for mechanical delivery devices, including prefilled syringes, with responsibility for DHF maintenance, traceability, lifecycle documentation, and product improvements.
Plan, coordinate, and execute laboratory testing for device characterization, verification, design transfer, fill-finish support, and technical investigations.
Develop, execute, and document test methods, protocols, technical assessments, and reports using sound engineering principles and GMP documentation practices.
Ensure testing activities are clearly linked to user needs, design inputs, product requirements, risk controls, specifications, and verification objectives.
Analyze and interpret experimental data using engineering judgment and statistical tools to support technical decisions, investigations, design changes, and specification assessments.
Support root cause analysis, failure investigations, deviations, nonconformances, risk assessments, and design or manufacturing change evaluations.
Partner with engineering, quality, manufacturing, operations, and scientific teams to support product enhancements, launch activities, inspection readiness, and cross-functional deliverables.
Contribute to continuous improvement efforts that strengthen lab efficiency, testing reliability, documentation quality, traceability, and project visibility.
Use tools such as Smartsheet, Excel, electronic lab notebooks, data analysis platforms, and AI-enabled productivity tools to improve project coordination, workflow management, communication, and operational efficiency.

Basic Qualifications:

Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Bioengineering, or a related engineering or scientific discipline.
Experience working in a regulated laboratory, medical device, pharmaceutical, biotechnology, or combination product environment.
Ability to independently plan, execute, document, and evaluate technical work using sound engineering or scientific principles.
Experience supporting laboratory testing, technical assessments, investigations, or product development activities.
Experience authoring or reviewing technical documentation in a regulated environment, such as protocols, reports, assessments, or investigation summaries.
Strong organizational skills with the ability to manage multiple priorities, maintain accurate records, and follow through on commitments.
Effective written and verbal communication skills with the ability to collaborate across technical and cross-functional teams.

Preferred Qualifications

Bachelor’s degree or higher in a relevant engineering or scientific field
Experience with medical device, combination product, or regulated product development, particularly within a design control environment.
Familiarity with design controls and traceability across user needs, design inputs, product requirements, risk controls, specifications, and verification/validation activities.
Understanding of how intended use, user needs, and risk management inform testing strategies, requirements, and design decisions.
Experience supporting Design History File documentation, traceability matrices, design verification, design changes, or lifecycle management activities.
Hands-on laboratory experience with device characterization, test method development, fixture design, GR&R, or mechanical testing.
Experience with Instron force testers, BlueHill Universal, electronic lab notebooks, and statistical analysis tools such as Minitab or JMP.
Experience supporting investigations, deviations, nonconformances, root cause analysis, risk assessments, or change control records.
Experience using digital tools such as Smartsheet, Excel, data visualization tools, electronic lab notebooks, or AI-enabled productivity tools to improve project tracking, workflow efficiency, documentation quality, and team communication.
Strong technical writing, presentation, and stakeholder communication skills.
Ability to work independently and collaboratively across dynamic, cross-functional teams while supporting complex workstreams under demanding timelines.

Understanding of applicable regulations and standards, including:

21 CFR 820 – Quality System Regulation
ISO 13485 – Quality Management Systems for Medical Devices
ISO 14971 – Risk Management for Medical Devices
EU Medical Device Regulation 2017/745

Basic Qualifications:

Master degree OR
Bachelor degree and 2 years of experience OR
Associate degree and 6 years of experience OR
High school diploma / GED and 8 years of experience

Must Have Skill Sets:

Hands-on device testing and lab execution
Experience working in a regulated design control environment
Strong technical documentation, data analysis, and digital tool skills

Day to Day Responsibilities:

Execute hands-on laboratory testing and device evaluations.
Analyze and document technical data, results, and observations.
Troubleshoot issues and support investigations, root cause analysis, and design changes.
Maintain documentation and traceability within a regulated design control environment.
Collaborate with cross-functional teams to support product improvements and project execution.
Use digital tools to manage data, documentation, workflows, and communication.

About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.

"US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran"

AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.

About the Company

US Tech Solutions, Inc.

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