×
Register Here to Apply for Jobs or Post Jobs. X

Packaging Engineer: Surgical Robotics – OTTAVA

Job in Santa Clara, Santa Clara County, California, 95053, USA
Listing for: 6267-Auris Health Inc. Legal Entity
Full Time position
Listed on 2026-05-31
Job specializations:
  • Engineering
    Packaging Engineer, Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Staff Packaging Engineer: Surgical Robotics – OTTAVA

Job Title

Staff Packaging Engineer – OTTAVA

Location

Santa Clara, California, United States of America

Purpose

The Staff Packaging Engineer supports the design, development, testing, and validation of packaging systems for medical devices, including robotic capital and durable medical equipment distributed globally. This role focuses on hands‑on execution of packaging solutions within a regulated medical device environment, ensuring protection of product quality, regulatory compliance, manufacturability, and cost effectiveness.

Key Responsibilities
  • Technical Lead for Packaging Design & Development
    • Provide technical guidance and influence packaging strategy, standards and guidelines across projects.
    • Design and develop primary, secondary, tertiary, and transport packaging for medical devices, accessories, and capital equipment.
    • Develop packaging specifications, drawings, and bills of materials.
    • Support structural design, cushioning concepts, blocking and bracing, and material selection using corrugated, foam, plastics, wood, and steel‑based solutions.
  • Testing, Validation & Quality
    • Execute packaging testing and validation activities per ASTM, ISTA, ISO, and internal procedures.
    • Support IQ/OQ/PQ execution, distribution simulation (drop, vibration, compression, shock), and accelerated aging studies (ASTM F1980).
    • Ensure documentation is complete, accurate, and traceable within the DHF and DMR.
  • Regulatory & Compliance
    • Ensure packaging designs comply with FDA QSR (21 CFR Part 820), ISO 13485, ISO 14971, and applicable global packaging standards.
    • Support packaging‑related content for regulatory submissions and participate in FDA or Notified Body audit activities as needed.
    • Ensure compliance with labeling, UDI, ISPM 15, RoHS, and REACH requirements where applicable.
  • Cross‑Functional & Supplier Collaboration
    • Collaborate with R&D, Quality, Regulatory, Manufacturing, Procurement, and Logistics teams throughout development and launch.
    • Support supplier qualification activities, packaging trials, and engineering change execution through PLM systems.
  • Continuous Improvement & Sustainability
    • Support cost, quality, and sustainability initiatives including material optimization, waste reduction, logistics efficiency, and recycled content usage.
    • Contribute to SOPs, work instructions, and continuous improvement efforts aligned with sustainability and PPWR objectives.
Qualifications
  • Education
    • Minimum a Bachelor’s degree; preferred focused degree in Packaging Engineering, Mechanical Engineering, Materials Science, or related discipline.
    • Advanced degree (Master’s) preferred.
  • Experience
    • Minimum six (6) years of relevant professional work experience.
    • Hands‑on experience in capital large system packaging and in medical device industry.
    • Working knowledge of ASTM, ISTA, ISO, and global packaging test standards.
    • Experience executing packaging validation, distribution testing, and technical documentation.
    • Familiarity with FDA QSR, ISO 13485, ISO 14971, and medical device quality systems.
    • Proficiency with CAD tools (e.g., Solid Works) and PLM systems for ECO management.
    • Experience supporting capital or robotic medical equipment packaging.
    • Knowledge of regulatory, sustainability requirements and standards for EU, Japan, Korea, and China (EPR).
    • Exposure to regulatory submissions (FDA 510(k), PMA, or EU MDR technical files).
    • Professional certifications such as CPP, RPT, ASQ, PMP, or Lean Six Sigma desirable.
    • Experience in manufacturing/supply chain domains with cross‑functional collaboration.
  • Additional Requirements
    • May require up to 20% domestic and/or international travel.
    • Fully onsite attendance required.
Compensation

Base salary range: $ – $.

Equal Opportunity Employer Statement

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, or other characteristics protected by federal, state or local law. Johnson & Johnson is committed to providing an inclusive interview process for applicants with disabilities and offers accommodations upon request.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary