September 18, 2024

Cardinal Health

Tijuana

OTHER

Principal Molding Engineer

What Manufacturing Engineering contributes to Cardinal Health

Define, validate, and document manufacturing processes with optimal use of resources, ensuring the level of quality, productivity and minimizing waste (scrap), continually improving the capacity of processes to meet specifications. Give direct support to production, by identifying cost reduction, generating ideas, solving and coordinating work teams, risk analysis, solution coordination, definition of processes, project planning, mentoring techniques and focused on providing sustainable technical solutions.

Role Responsibilities:

Design and implement the processes that comply with the product requirements and high operational performance.
Document all processes according to the ISO Quality system and FDA
Respond opportunely to the LAPS, identifying the root cause of the deviations to the system Identify and minimize the sources of Scrap.
Plan and execute OPEX projects
Design technical and operational training
Keep the PFMEA updated
Execute the process validations according to the MVP
Define capacity increase needs
Support new product projects
Solution of productivity and scrap quality problems by applying analysis and optimization techniques
Keep the cost of products updated
Comply with the necessary security measures to prevent accidents, occupational diseases and environmental contingencies within the company.
Comply with the environmental measures established in the Internal Work Regulation.
Coordinate and implement the QIP / COS initiative in the process area.
Effective Team Building
CAPEX project management (Capital and Expenses).
Generate engineering documentation to support validations and engineering change.

Minimum Qualifications

Bachelor’s degree in Engineering
+5 years of experience in similar position
Advanced English

Knowledges:

New Product Introduction, Product Transfer, Agile, BPCS, Product Costing, Patient Focused, Ms Project, Process and Product validations, Project Management, Six Sigma, Lean Manufacturing, ISO13485 / ISO9001, FDA or equivalent.
Functional Competencies
Problem resolution
Self-directed
Proactive
Leadership
Accountable
Development Direct Reports and Others
Delegation
Managing and measuring work
Confronting Direct Reports
Motivating Others
Strategic Agility

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

Design and implement the processes that comply with the product requirements and high operational performance.
Document all processes according to the ISO Quality system and FDA
Respond opportunely to the LAPS, identifying the root cause of the deviations to the system Identify and minimize the sources of Scrap.
Plan and execute OPEX projects
Design technical and operational training
Keep the PFMEA updated
Execute the process validations according to the MVP
Define capacity increase needs
Support new product projects
Solution of productivity and scrap quality problems by applying analysis and optimization techniques
Keep the cost of products updated
Comply with the necessary security measures to prevent accidents, occupational diseases and environmental contingencies within the company.
Comply with the environmental measures established in the Internal Work Regulation.
Coordinate and implement the QIP / COS initiative in the process area.
Effective Team Building
CAPEX project management (Capital and Expenses).
Generate engineering documentation to support validations and engineering change.

Minimum Qualifications

Bachelor’s degree in Engineering
+5 years of experience in similar position
Advanced English

Knowledges:

New Product Introduction, Product Transfer, Agile, BPCS, Product Costing, Patient Focused, Ms Project, Process and Product validations, Project Management, Six Sigma, Lean Manufacturing, ISO13485 / ISO9001, FDA or equivalent.
Functional Competencies
Problem resolution
Self-directed
Proactive
Leadership
Accountable
Development Direct Reports and Others
Delegation
Managing and measuring work
Confronting Direct Reports
Motivating Others
Strategic Agility