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Sr Packaging Engineer - Exempt

Key Facts

Remote From: 
Canada, California (USA)
Full time
English

Other Skills

  • •
    Report Writing
  • •
    Communication
  • •
    Teamwork
  • •
    Analytical Thinking
  • •
    Mentorship
  • •
    Problem Solving

Roles & Responsibilities

  • Bachelor's degree in BioMedical, Mechanical, Industrial, Manufacturing, Packaging, or related engineering field.
  • 4-7 years of relevant experience with a BS degree; 2 years with an advanced degree.
  • Experience in designing and validating sterile medical devices, particularly sterile threaded containers.
  • Strong skills in supporting documentation, drafting test protocols and reports, and creating specifications for approval.

Requirements:

  • Design, develop, and test a variety of containers for the protection, display, and handling of products.
  • Determine packaging specifications based on product nature, cost limitations, legal requirements, and required protection levels.
  • Consider external variables such as moisture, corrosive chemicals, temperature variations, light, heat, rough handling, and tampering in packaging designs.
  • Manage documentation and coordinate Good Manufacturing Practices (GMPs).

Job description


We are seeking a highly skilled and experienced professional to join our team in Virtual, CA, a vibrant and innovative environment that offers a perfect blend of professional opportunities and quality of life. This location is ideal for those who appreciate the flexibility of remote work while being part of a dynamic community.

Key Responsibilities

  • Design, develop, and test a variety of containers for the protection, display, and handling of products.
  • Determine packaging specifications based on product nature, cost limitations, legal requirements, and required protection levels.
  • Consider external variables such as moisture, corrosive chemicals, temperature variations, light, heat, rough handling, and tampering in packaging designs.
  • Design package exteriors with product identification, sales appeal, and aesthetic quality in mind.
  • Manage documentation and coordinate Good Manufacturing Practices (GMPs).
  • Support prototype line development in manufacturing facilities/plants.

Qualifications

  • Bachelor's degree in BioMedical, Mechanical, Industrial, Manufacturing, Packaging, or related engineering field.
  • 4-7 years of relevant experience with a BS degree; 2 years with an advanced degree.
  • Experience in designing and validating sterile medical devices, particularly sterile threaded containers.
  • Strong skills in supporting documentation, drafting test protocols and reports, and creating specifications for approval.
  • Proven ability to work collaboratively in teams, effectively communicate, and divide responsibilities.

Work Environment

This position requires a minimum of 4 days per week on-site in Santa Ana, with the flexibility to work from home 1 day per week. The ideal candidate should be within a 1-hour commute of the Santa Ana site.

Additional Information

As a seasoned individual contributor, you will work independently under limited supervision, coach and review the work of lower-level specialists, and manage projects/processes. You will contribute to the completion of work group objectives, build relationships, and reach consensus on assignments. Your role will involve innovative problem-solving, process improvements, and in-depth analysis, often providing recommendations on process improvements.


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