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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in packaging design and development within the medical device industry, focusing on innovative solutions that meet user needs and comply with regulatory standards. Proficient in managing project timelines and applying design controls to ensure successful product launches.
Highest-signal resume keywords
Packaging DesignProject ManagementDesign ControlsMedical Device Industry ExperienceISO 11607-1 Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Mechanical EngineeringBiomechanical EngineeringPrototype DevelopmentTechnical Report WritingDesign VerificationDesign ValidationSurgical Procedures KnowledgeProduct LaunchCross-Functional Team LeadershipQuality Management
Soft Skills
Problem-SolvingCommunicationCollaborationMultitaskingDecision-Making
Industry Keywords
Medical DeviceRegulated IndustrySterile PackagingUser Needs AssessmentDesign Issues Management
About the role
Key responsibilities & impact- Design packaging and participate in or lead cross-functional teams from packaging design and development through product launch
- Integrate new products into Stryker’s Trauma & Extremities packaging systems following company acquisitions
- Develop innovative packaging for new products based on user needs and current packaging design and development procedures
- Develop prototypes for design verification and validation
- Work with clinical advisors to gather input on the design and evaluation of new packaging
- Apply and manage design controls
- Write technical reports
- Develop new packaging, address design issues, and maintain existing packaging
- Apply knowledge of surgical procedures to develop innovative customer-focused solutions
- Develop and manage project plans and timelines in accordance with design control guidelines
Requirements
What you’ll need- Bachelor’s degree in science, mechanical/biomechanical engineering, quality management, or manufacturing engineering
- 2+ years of experience in an engineering role, preferably in packaging engineering or biomechanical laboratory testing
- Demonstrated ability to lead complex initiatives from concept through release
- Business-level fluency in English, both written and spoken
- Prior experience in the medical device industry or another highly regulated industry preferred
- Experience working with sterile packaging in accordance with ISO 11607-1 preferred
- Ability to work on multiple subtasks in parallel preferred
- Ability to make complex decisions with guidance preferred
- Ability to multitask and to think on your feet preferred
- Strong problem-solving, communication, and collaboration skills preferred
- Willingness to work at least two days per week on site at either Montbonnot-Saint-Martin (38), France, or Cork, Ireland
- Travel up to 20%
Benefits
Comp & perks- Competitive salary and benefits commensurate with your job
- Personal and internal career development, with possibilities for vertical and lateral position movement
- Recognition and awards for outstanding individual and cross-functional team performance
- Employee Resource Groups providing development, networking, collaboration, inclusion, and belonging opportunities
- Employee referral program
- Potential incentive compensation such as bonus and/or commissions where applicable
- Comprehensive benefits package
