Principal Engineer Mechanical Design

States considered:

Role Description

POSITION SUMMARY

The Principal Mechanical Design Engineer (Pr. DE) will work as a key member of the research and development (R&D) mechanical design engineering (MDE) team in the design development testing and integration of electromechanical automated biodevice products. This position requires a highly creative innovative and seasoned leader with a proven track record in creating new product concepts and a strong ability to transform concepts into realizable product. The Pr. DE has the primary responsibility from Proof of Concept (POC) through to completion of the prototype phase (Alpha) and may act as Project Team Lead (PTL). The Pr. DE will apply best practice development strategies with advanced technical problemsolving techniques and have a history of working within crossfunctional teams to resolve issues throughout the product development life cycle.

This role will provide technical leadership and influence the design efforts of other engineers as well as drive the development team to create optimal products while adhering to committed project plans. The Pr. DE will also work crossfunctionally with internal and external teams to define and ensure customer and product requirements are met while scaling the product for a successful market launch.

POSITION RESPONSIBILITIES

The Pr. DE has wide and farreaching responsibilities including:

• Responsible for conceptual design & development of system architecture through completion of the functional prototype phase (alpha) milestone of the stage gate process.
• Design integration testing and deployment of automation systems for handling conveyance vaccine/drug delivery and assessments/treatments of biological entities.
• Design and development of electromechanical systems and mechanisms fluid pneumatic and hydraulic drive systems while understanding the interface to electrical control systems and underlying biological process needs.
• Facilitate concept and technology development strategies for new biodevice products including establishing POC feasibility goals and protecting associated intellectual property.
• Communicate complex technical strategies in an understandable way to all organization levels.
• Apply the stagegate development process for new product development and create deliverables in accordance with the process.
• Provide technical guidance to ensure robust and reliable designs are developed with seamless integration of mechanical electrical and software subsystems.
• Ensure designs meet or exceed product specifications regulatory requirements and international standards.
• Collaborate with cross function teams (product engineering biology testing/reliability electrical engineering controls engineering manufacturing quality and service) to develop innovative products and processes for Biodevice products.
• Identify and develop new and emerging technologies as well as internal/external competencies and develop these technologies into product concepts to advance Biodevice products.
• Function as technical liaison to suppliers and key stakeholders.
• Work with project teams to identify and mitigate development risks.
• Perform assessment of system level risks proposing evaluating and implementing mitigations using Failure Modes and Effects Analysis (FMEA) methods.
• Develop design specifications conduct engineering parameter assessments develop test plans and application of design robustness disciplines.
• Oversee the development of detailed drawings BOMs and release in collaboration with the CAD and PLM teams.
• Seek strategic opportunities to build new product offerings across the portfolio consistent with the Zoetis strategy to drive a continuum of care (predict prevent detect and treat) in addressing unmet customer needs.

EDUCATION AND EXPERIENCE

• B.S. in Mechanical Engineering required MSME preferred. Minimum of 10 years demonstrated engineering experience in a complex product development environment.
• Strong first principles mechanical engineering knowledge and skills with minimum 5 years in lead engineering role.Previous experience with automated biodevice equipment highly desired.
• Continuous Improvement Certifications such as Design for Six Sigma (DFSS) and/or Manufacturing Six Sigma (MSS) a plus
• Prior experience in a regulated industry such as healthcare medical devices or pharmaceutical companies desirable.

TECHNICAL SKILLS REQUIREMENTS

• Prior experience in a technical leadership role involving development of complex automation systems
• Demonstrated experience in developing automation systems preferably involving biological applications using fundamental machine design principles
• Demonstrated proficiency in electromechanical design modeling simulation and tolerance analysis.
• Thorough understanding and demonstrated experience with requirements decomposition development of engineering product specifications and risk management
• Broad engineering knowledge and understanding of extensive new product introduction quality management system manufacturing operations and product lifecycles
• Experience and proficient with SolidWorks 3D Design Software or similar
• Comprehensive understanding of GD&T and best design and drawing practices ASME Y14.5 Y14.100.
• Knowledge of materials fabrication processes metrology principles and machine shop practices
• Knowledgeable in 3D printing rapid prototyping and modern engineering techniques for development.
• Experience with advanced automated systems with optical electrical mechanical software pneumatic and fluid subsystems.
• Demonstrated experience in critical thinking and problemsolving skills planning and organizing decisionmaking.
• Knowledge in techniques such as Design for Six Sigma (DFSS) Manufacturing Six Sigma (MSS) Design for Reliability (DFR) Design for Manufacturability and Assembly (DFMA) and Design for Serviceability (DFS)
• Team player with excellent communication skills who can challenge motivate and drive team members to think outside of the box.
• Flexible and Adaptive; able to explore many concepts concurrently.

Full time

Regular

Colleague

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