Associate Project Engineer

Position Title: Associate Project Engineer
Department: Product Development
Reports To: Director of Product Development
Job Type: Full Time
Shift: Monday - Friday 09:00 AM - 05:00 PM
Exempt / Non-Exempt: Exempt

Purpose:

The Associate Project Engineer will support the management and development of new and existing products. This will include product development, processing, testing, and marketing as well as equipment management associated with products.

 

Duties & Responsibilities:

  • Support the development of new products in collaboration with the project team, Quality Assurance and Operations departments
  • Develop scalable and repeatable manufacturing processes for new products in collaboration with the Quality Assurance (QA) and Operations departments
  • Author and revise standard operating procedures (SOP) according to FDA, AATB, and other regulations if applicable
  • Perform processing of human tissue as part of the development of new products and processes
  • Support the development and implementation of sales material for products and collaborate with QA/RA to ensure all claims are appropriate for market and regulatory position
  • Design and execute scientific experiments for product development projects. Complete data collection, evaluation, and interpretation of results to generate statistically significant data to support project decisions and/or product launch. Experimentation may extend to in-vitro or in-vivo assays conducted in-house or externally sourced
  • Communicate and negotiate with new or existing vendors to source and implement testing, equipment, supplies, materials, or other resources to support research project activities
  • Assist the Operations department in the maintenance, assembly, installation, or implementation of new equipment or process specific tooling
  • Design, order, evaluate, and onboard new proprietary equipment in support of manufacturing. Assist in the maintenance/calibration of new equipment
  • Assist in the development, drafting, and execution of verification and validation protocols in accordance with regulatory requirements and industry best practices
  • Assist with training and technology transfer for new projects and products
  • Assist in the development and maintenance of the project schedule for assigned projects
  • Ensure quality and quality control within their assigned projects
  • Assist with investigation of quality events and determine appropriate containment, preventive/corrective actions
  • Develop working knowledge of FDA, AATB, and ISO regulatory requirements
  • Maintain effective communication with the project team on progress and challenges related to project tasks
  • Perform other related duties as assigned

 

Skills & Abilities:

  • Organized and self-motivated
  • Excellent attention to detail
  • Strong analytical and creative thinking skills
  • Effective communication and technical writing skills
  • Ability to present complex ideas
  • Ability to work in a fast-paced environment
  • Ability to work independently and in a team environment
  • Competent in project management
  • Proficient in Microsoft Office

 

Education & Experience:

  • Bachelor`s degree (or current enrollment) in an Engineering, or Biological science or related field required
  • Experience with Mechanical Design
  • Experience with CAD Software
  • Experience or Knowledge in Project Management
  • Entry Level Position