Principal Engineer R&D Lead

hace 3 semanas

Tijuana, Baja California, México Cardinal Health A tiempo completo

Job Summary:

The Principal RD Engineer II is a key member of the new product development PMO, supporting program managers and R&D groups on new product development and product change programs. This role ensures manufacturing approaches align with customer and product specifications.

Key Responsibilities:

  • Process Development & Design Transfer: Develop, implement, and monitor manufacturing and assembly process development initiatives aligning with strategic goals. Lead Design for Manufacturing/Assembly/Service assessments and activities to ensure alignment with R&D, Corporate Engineering, Operations, and Quality teams.
  • Supplier Selection: Represent PMO/R&D in identifying and evaluating potential suppliers. Provide senior leadership and core teams with supplier/partner recommendations based on on-site business assessments, focusing on supplier gap analysis and development plans.
  • Collaboration: Collaborate with corporate engineering, suppliers, and manufacturing partners to identify, select, qualify, and implement manufacturing equipment and processes aligning with customer, product, and business goals. Act as a liaison between suppliers, manufacturing partners, and the NPD team to communicate project status and monitor risks, issues, and timeline milestones.
  • Develop product and process costs (COGS), in tandem with operations and sourcing teams, validating and monitoring cost goals throughout the development and product launch cycle.
  • Implement Six Sigma/Lean Tools on NPD and product change programs.
  • Guide and support core and extended team members in identifying and applying appropriate DFSS/Lean elements.
  • Understand GMP and ISO requirements related to manufacturing and quality.

Requirements:

  • BS degree in Mechanical Engineering, Electrical Engineering, or related field.
  • Advance English and Spanish.
  • 5+ years of demonstrated experience in OpEx / Manufacturing, Product/Process Development, and Process Improvement implementation.
  • Experience in a highly regulated manufacturing environment.
  • Expertise in manufacturing, supplier development, risk/issue management, implementation planning, training, and communication from an OpEx / Mfg perspective.
  • Experience in a new product development and product change environments to ensure a clear translation of product design requirements into process requirements to support critical to quality design elements.
  • Proven track record of collaborating with, influencing, and negotiating with all levels of an organization and external organizations.
  • Strong conflict resolution skills and the ability to influence without authority.
  • Strong analytical and statistical problem-solving tools.
  • Ability to work successfully in complex and emerging business and project areas, leveraging interpersonal and technical skills to optimize results.
  • Ability to work in a team setting as well as independently with all levels of managers, associates, clients, and customers.
  • Solid proficiency in software programs such as Minitab, Microsoft Word, PowerPoint, Excel.
  • Excellent oral/written communication and presentation skills.

Preferred Qualifications:

  • Medical device manufacturing/development experience is a plus.
  • Molding and extrusion experience.
  • PMP certification is highly preferred.
  • Mastery of Six Sigma principles is preferred.
  • Working knowledge and experience in Lean Implementation is preferred.
  • Plastic transformation & assembly, and molding/extrusion engineering experience preferred.
  • Experience with capacity planning preferred.

Organizational Relationship/Scope:

This position reports to the Manager of Project Engineering within the NPD PMO and is part of the Global R&D organization.

Working Conditions:

25% travel (Domestic & International).

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