Intern
Stryker
This listing was originally posted on Stryker's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Upgrade to Pro — $25/moKEY RESPONSIBILITIES
· Support packaging design and development activities for new and existing products.
· Assist in creating and updating packaging drawings, specifications, bills of materials (BOMs), and technical documentation.
· Participate in packaging testing activities such as drop, vibration, compression, transit, and other performance tests.
· Support packaging change management, sustaining engineering, and continuous improvement projects.
· Collect, analyze, and document packaging-related test data and project information.
· Assist in preparing technical reports, presentations, and project updates.
· Coordinate with cross-functional stakeholders and suppliers to support project execution.
· Support cost optimization, standardization, sustainability, and packaging improvement initiatives.
ELIGIBILITY
· Pursuing a Post Graduate Diploma in Packaging (PGDP) or equivalent packaging program from IIP.
· Strong academic record and interest in packaging engineering and product development.
· Basic understanding of packaging materials, packaging systems, testing methods, and package development.
· Knowledge in Microsoft Excel, Word, and PowerPoint.
· Good written and verbal communication skills, with the ability to work effectively in a team.
PREFERRED SKILLS
· Exposure to CAD tools such as Creo, SolidWorks, or AutoCAD is an advantage.
· Basic understanding of packaging validation, engineering drawings, and documentation practices.
· Strong analytical, problem-solving, organizational, and learning abilities.
· Self-driven and comfortable working in a cross-functional, quality-focused environment.
LEARNING OPPORTUNITIES
· Medical device packaging design and development.
· Packaging testing, validation, and technical documentation.
· Change management and sustaining engineering processes.
· Quality and regulatory compliance in a regulated industry.
· Cross-functional project collaboration and stakeholder management.
· Packaging sustainability and continuous improvement initiatives.
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MEDICAL DEVICES
Medical Devices
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