
Search by job, company or skills
. Define, plan and lead activities for test method & measurement system development and validation, and testing optimization in support of Design Verification.
. Lead creation and execution of verification protocols, summarize results, enable formal design reviews, and own the verification portion of the Design History File.
. Demonstrate proficiency in spotting Design Variance through relevant statistical measures.
. Follow Design Control & ensure compliance with all local, state, federal, international, and internal safety regulations, policies, and procedures.
. Interpret and analyze design verification data with respect to product performance and operational stability in the manufacturing plants.
. The associate will work on receipt, preparation, testing, and delivery of test samples and support materials for all V&V lab associate testing including sample inventory management.
. Application of engineering first principles and advanced engineering methods to gain deep understanding of the underlying technical issues, and to propose and implement robust solutions.
. Collaborate with Design & Development, Systems Engineering and cross-functional teams to ensure product requirements are verifiable and measurable.
. Synthesize, develop, update, and optimize designs based on understanding design space. Understand design options and tradeoffs managing critical parameters leverage strong engineering fundamentals and tools. Incorporate manufacturing principles early in the development process.
. Executes Continuous Improvement projects in the following (but not limited to) areas.
. Equipment or method troubleshooting/repairs.
. Coordinates with Test Method Development and Verification & validation team for equipment and method validations
. Method or Equipment Upgrades
. Fixture maintenance
. Drawing or Specification modifications
. Responsible for Complete end to end maintenance of test equipment and management of Test method validation records.
. Ensure deliverables are reliable across the design space, is adequately pressure-tested to satisfy user, regulatory and business requirements. Understand system and subsystem design sensitivity and identify and address early any potential design integration and transfer risks.
. Implement DFSS rigor throughout the design selection and development process, leveraging and deploying empirical, statistical, and analytical tools to drive informed design decisions and reduce design iteration cycle times.
. Ensure the design considerations are embedding all applicable DFX (Design for Excellence) aspects including manufacturability, usability, reliability, and safety.
. Create and document novel test methodologies and provide feedback and recommendations for product/design changes.
. Actively build on personal skills, expertise, and competencies. Ensure that technical lessons are reviewed, learned, and disseminated.
. Coach and mentor junior engineers and technicians to execute project deliverables.
. Ensure compliance with BD quality policies, procedures, and practices.
. Ensure compliance with all local, state, federal, and BD safety regulations, policies, and procedures.
. The incumbent will also be responsible for ensuring QMS conformance and ensure that the quality policy and objectives are met per organizational guidelines.
. Coordinate the Material Shipment & Vendor management.
Education and Experience:
Bachelor's degree in mechanical or biomedical Engineering with 5 to 8 years of experience in medical device or other regulated industry OR Master degree in mechanical or biomedical Engineering and 4+ years of experience.
Knowledge and Skills:
. Expertise with test method development, validation strategy, and execution is required.
. Expertise in fixture design & development.
. Expertise with design verification & validation strategy development and execution is required.
. Strong track record of technical problem solving and effective product development through expert application of engineering principles is required.
. Design controls expertise and experience with traditional and modern fabrication techniques is required.
. Proven experience in leading CAPAs, design-defect analyses, managing non-conformances and remediation is required.
. Proficiency in solid mechanics/mechanics of materials and proficiency statistical methods/tools is required.
. Experience with design standard methodologies, including advanced tolerance design, and design for reliability.
. Experience and Knowledge on Medical regulatory standards
. Experience in solid modeling (SolidWorks) or electromechanical systems is a plus.
. Experience in high-volume manufacturing processes is a plus.
. Experience developing and commercializing medical devices is a plus.
. Exposure to Chemistry/ Chemical Engineering and/or structural analysis and simulation/mathematical modeling desirable.
. DFSS training or certifications are a plus.
Preferred skills:
. Ability to lead and teach others to assess project/program needs, formulate strategy, build support, and execute initiatives.
. Strong interpersonal and decision-making skills and the ability to effectively manage change and uncertainty.
. Ability to engage and mentor team members and to maximize diverse perspectives to achieve the best outcomes.
Required Skills
Optional Skills
.
Job ID: 142752981