What are the responsibilities and job description for the Packaging Engineer position at Suru?
Packaging Engineer (Implantable Orthopedics)
Job Description
Our client is seeking a Staff Packaging Engineer to support both New Product Development (NPD) and sustaining engineering initiatives for a portfolio of implantable medical devices. This individual will serve as a key member of the packaging engineering team, driving packaging design, development, validation, supplier management, and cross-functional collaboration throughout the product lifecycle.
This is a highly visible role requiring someone who is comfortable balancing multiple priorities in a fast-paced environment. The ideal candidate will have experience working with Class II or Class III implantable medical devices, with orthopedic device experience being highly preferred. Success in this role requires strong technical expertise, excellent communication skills, and the ability to work across engineering, operations, quality, supply chain, and external manufacturing partners.
Day-to-Day Responsibilities
- Lead packaging development activities for new product development and sustaining engineering projects.
- Design, develop, and validate sterile packaging systems for implantable medical devices.
- Execute packaging validation activities in accordance with applicable regulatory and industry standards.
- Manage multiple concurrent projects (typically 6–12) while balancing competing priorities and timelines.
- Collaborate cross-functionally with R&D, Manufacturing, Quality, Regulatory Affairs, Supply Chain, and Operations teams.
- Work directly with contract manufacturers and packaging suppliers to support product development, supplier performance, and continuous improvement initiatives.
- Drive packaging strategy while considering cost optimization, manufacturability, supply chain impacts, and product performance.
- Participate in project planning, timeline management, and cross-functional coordination to ensure successful project execution.
- Ensure compliance with MDR requirements and applicable medical device packaging standards throughout the product lifecycle.
Requirements / Qualifications
Required:
- Bachelor's degree in Packaging Engineering, Mechanical Engineering, Biomedical Engineering, or a related technical discipline.
- 4–10 years of packaging engineering experience within the medical device industry.
- Experience supporting implantable Class II and/or Class III medical devices.
- Hands-on experience with packaging design, development, and validation.
- Knowledge of medical device packaging regulations and validation standards.
- Experience working in cross-functional product development environments.
- Strong communication and organizational skills.
- Ability to manage multiple projects simultaneously in a fast-paced environment.
Preferred:
- Orthopedic medical device experience.
- Experience supporting both New Product Development (NPD) and sustaining engineering.
- Experience managing external packaging suppliers or contract manufacturers.
- Familiarity with Medical Device Regulation (MDR) requirements.
- Exposure to project management activities, including project planning, prioritization, scheduling, and cross-functional coordination.