Ventura Solutions

Senior Systems Engineer

Ventura Solutions  •  San Diego, CA (Onsite)  •  3 hours ago
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Job Description

We are seeking an experienced Senior Systems Engineer to support client device development programs focused on autoinjector and combination products. The successful candidate will serve as an extension of the client team, leading day-to-day development activities, managing design control deliverables, coordinating external partners, and ensuring program objectives are achieved.

The ideal candidate brings deep hands-on experience in medical device and combination product development, with the ability to independently manage design control activities, risk management deliverables, technical documentation, and cross-functional project execution while contributing to overall program strategy.

Responsibilities

  • Support autoinjector and combination product development activities across multiple programs.
  • Develop and maintain integrated project schedules and Gantt charts.
  • Coordinate activities across device vendors, fill-finish partners, assembly sites, and other suppliers.
  • Prepare and manage design control and risk management deliverables.
  • Draft development plans, verification plans, and supporting technical documentation.
  • Manage day-to-day execution of assigned programs while receiving strategic direction from client leadership.
  • Work independently on design control processes and deliverables.
  • Communicate effectively across technical and cross-functional teams.

Qualifications

  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related discipline.
  • Approximately 7–10 years of relevant experience in device or combination product development.
  • Direct, hands-on autoinjector development and commercialization experience.
  • Experience with combination product design controls and risk management.
  • Willingness and ability to perform detailed, hands-on execution work in addition to any strategic input.
  • Strong project management skills, including schedule development and cross-functional coordination.
  • Strong written and verbal communication skills.

Location

  • On-site in San Diego, CA

Employment Type

  • W2 Contract

Benefits for W2

  • Medical and dental insurance
  • Paid vacation time
  • 401(k) after 90 days

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com


Equal Opportunity Employer Minorities/Women/Veterans/Disabled

Ventura Solutions

About Ventura Solutions

Ventura Solutions provides End-to-End consulting, staffing, and training services for the Medical Device and Combination Products industry.

We provide consulting, staffing, and training solutions in the following areas:

-Design Controls

-Risk Management

-Verification & Validation

-Design and Development

-Project Management

-Quality

-Regulatory

-Human Factors

-DHF & Quality System Remediation

-Software as a Medical Device (SaMD)

-Statistics

-Clinical Affairs

-Market Access

-Funding

-NIH SBIR Grants

-Start-Ups

Ventura Solutions is your one-stop shop for getting your product to the market or keeping it compliant.

Detailed list of areas of expertise:

Medical Device & Combination Product Consulting

Design Controls, Risk Management, 21 CFR 820.30, ISO 13485, ISO 14971, Design and Development, Systems Engineering, Project Management, Quality Assurance, Human Factors, IEC 62366, Usability, Design Verification, Design Validation, Statistics, Design History File (DHF) Remediation, Software as a Medical Device (SaMD), Manufacturing, Change Control, Regulatory, FDA Q-Sub, Pre-Sub, Breakthrough Device Program (BDP), Investigational Device Exemption (IDE), 510(k), MDR

Medical Device Start-Up & Business Consulting

Co-Development Deals, Licensing Deals, Fundraising, Non-Dilutive Funding, NIH SBIR Funding, Mergers and Acquisitions (M&A), Commercialization, Valuations, Equity Distributions, Board of Directors, Leadership, Organizational Development, Building High Performing Teams, Concept Evaluation & Selection, FDA or EU Regulatory Strategy, Value Proposition

Staffing, Direct Placement, & Executive Recruitment

Medical Device Engineers, Risk Management Engineers, Systems Engineers, Human Factors Engineers, Design Verification & Validation Engineers; Test Method Development Engineers, Materials Engineers, Project Managers; Process Validation Engineers, Process Development Engineers, Quality Engineers, Design Assurance Engineers, Regulatory Affairs Specialists

Industry
Manufacturing & Production
Company Size
11-50 employees
Headquarters
Vernon Hills, IL
Year Founded
2016
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