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Project Engineer - Dermal Tissue

Project Engineer - Dermal Tissue

Extremity CareSan Antonio, TX, US
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Job Description

Job Description

Salary : Purpose

The Project Engineer will support existing and new products with project management and development. This will include product management, prototyping, testing, and marketing associated with products.

Responsibilities

  • Manage and execute product development projects from ideation to market launch
  • Lead project management activities on assigned projects including schedule, budget, work products and deliverables
  • Execute projects following design control practices and developing the necessary project inputs and outputs required for each development phase
  • Organize appropriate methods of communication between project stakeholders
  • Collect, organize, and communicate customer and market feedback to identify critical product characteristics
  • 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
  • Review, analyze, and characterize critical financial characteristics of products including COGS
  • Conduct group trainings for new processes and complete technology transfer of new products
  • Perform processing of human tissue as part of the development of new processes
  • 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
  • Specify, order, evaluate, and onboard new proprietary equipment in support of products
  • Execute and plan new company initiatives including equipment onboarding, supply chain management, distribution capability, and product support
  • Design and develop custom manufacturing equipment if applicable
  • Support and expand existing product lines by responding to business development needs, collecting, and organizing product feedback, and improving and supporting products
  • Support the development and implementation of sales material for products and work with Quality Assurance to ensure all claims are appropriate for market and regulatory position
  • Conduct literature reviews to support new and existing products
  • Assist with investigation of product quality events and appropriate preventative / corrective actions
  • Support regulatory and reimbursement submissions for products
  • Develop and execute validation protocols in accordance with regulatory requirements. Review validation data and draft validation reports
  • Identify and develop a working knowledge of ASTM, AAMI, ISO, and other necessary validation or testing guidance's required for assigned product development projects
  • Maintain a working knowledge of FDA 21 CFR 1271, FDA 21 CFR 820, AATB standards, ISO Standards, cGMP / CGTP, other relevant regulations / standards, and internal organizational policies and standard operating procedures
  • Travel domestically up to 5% to attend offsite meetings, conferences, and support business initiatives
  • Maintain acceptable attendance and punctuality for scheduled work hours and meetings
  • Ensure completion of assigned tasks and responsibilities within defined timeframes
  • Flexibility to work outside of normal business hours during weekdays or weekends with reasonable advance notice, to support business / operational needs when necessary
  • Perform other duties as assigned

Skills

  • Project Management experience
  • Ability to present complex ideas
  • Technical writing ability
  • Knowledge of manufacturing environment and validation procedures
  • Strong analytical and creative thinking skills
  • Ability to work in a fast-paced environment
  • Ability to work independently and in a team environment
  • Proficient in Microsoft Office
  • Experience working with vendors and suppliers
  • Qualifications / Requirements

  • Bachelor's degree in biomedical or mechanical engineering or related field required
  • 3 years of experience in project management required
  • Experience with Mechanical Design preferred
  • Experience with CAD Software preferred
  • Education in Engineering, or Biological Science or related field preferred
  • Product Development and exposure to medical products preferred
  • Experience with allografts and / or medical devices preferred
  • Clearance of favorable background investigation required
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