AstraZeneca logo

Associate Principal Packaging Engineer

AstraZeneca
Full-time
Remote friendly (Durham, NC)
United States
Operations

Want to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now — JobsAI.

Role Summary

Packaging Development Associate Principal Engineer (Design controls / Combination products) based in the Pharmaceutical Technology and Development (PT&D) department. This role supports the entire PT&D portfolio, delivering packaging strategy and supporting development projects from Phase 1 to transfer to Commercial Manufacture.

Responsibilities

  • Lead the design & development, and testing of all packaging presentations for medical devices and combination products to achieve project targets in a timely fashion.
  • Develop innovative, creative, and cost-competitive packaging solutions that meet patient needs, sustainability objectives, and quality standards.
  • Generate and review regulatory submission documents, plans, protocols, and reports ensuring project objectives are met (Design History File documentation).
  • Contribute and support relevant information to the Design transfer team to enable successful packaging transfer to AZ manufacturing operations and/or contract manufacturing sites.
  • Ensure work is performed in accordance with safety (SHE), quality, and compliance standards.
  • Influence understanding and interpretation of packaging regulations.
  • Represent specialist packaging area (SME) on Device Project Teams, providing data (technical, resource & budgetary).
  • Understand and influence developments within the industry.
  • Contribute to training and development of packaging colleagues by acting as coach/mentor as appropriate.

Qualifications

  • Minimum 7 years experience
  • BSc/PhD in Packaging Engineering, Mechanical Engineering, Biomedical Engineering, Materials Engineering, Chemical Engineering, or Pharmaceutical Sciences with related device/biopharmaceutical experience
  • Knowledge and application of cGMP requirements, Device and Combination Product requirements in major pharmaceutical markets (USA, Europe)
  • Strong technical and scientific skills with packaging solutions for parenteral and/or Inhalation products
  • Strong experience with medical device or combination product commercialization, operations support, and significant packaging materials/components knowledge
  • Lean Six Sigma Green Belt or higher certification with strong problem-solving skills
  • Demonstrated ability to manage multiple projects of variable complexity
  • Strong operational relationships with customers
  • Experience of leading cross-disciplinary delivery teams