Responsibilities
- Performs full equipment and mold validations to insure budgeted cost and quality levels are achieved.
- Prepares required documentation i.e., validation protocols/reports to meet quality system guidelines.
- Develops and performs DOE’s as required per the business needs.
- Collect and statistically analyzes data, and document results in process development, IQ, OQ, and PQ completion reports.
- Act as a key participant in DFMEA, PFMEA, and CTQ processes assuring specifications are well defined and documented.
- Conceptual leader for technology advances associated with tooling and process development.
- Communicate and coordinate activities with multiple functional groups both within and outside of operations.
- Assists supervisors and molding technicians to improve quality and output of molded components.
- Coordinates and performs hands on trouble shooting on molding issues with the tool/machine maintenance group.




- Supervises operating parameters of molds and related support equipment.
- Assures adherence to manufacturing tolerances.
- Directs the molding technicians in setting optimum molding parameters to achieve production volume goals at the lowest cost.
- Issues periodic status reports on molds and other related equipment.

Qualifications
- Bachelor’s Degree (B.A.) in mechanical engineering or plastics related degree from a four-year college.
- 3 to 5 years of experience in plastics molding, including validation and product development for a medical device manufacturer.
- Understanding of tool design, troubleshooting, and component qualification RJG Systematic molding training or scientific molding related certification preferred.

📌 Ingeniero de Moldeo (Tijuana)
🏢 Harmac, Medical Products, Tijuana
📍 Tijuana