Job Description
- Responsible for sampling and establishing processes for new and transfer tooling projects and their maintenance throughout the entire project life cycle using Medbio’s practices and principles for scientific molding.
- Provide resourceful input on cost reduction and minimization of machine generated scrap.
- Evaluate tooling for areas of concern, areas of improvement for quality and efficiency, and recommend improvements to optimize molding, setup, and overall manufacturing.
- Utilize statistical process control to help develop robust, repeatable, and reproducible injection molding processes along with improvements.
- Program robots and peripheral equipment.
- Mentor and develop associate members of the team.
- Provide process engineering support to all production processes.
- Exhibit safety awareness and safe work practices
- Assists in the implementation and/or improvement of new ideas, processes, and technologies.
- Responsible for interacting with management, engineers, maintenance, operators, and customers to resolve process related issues.
- Perform any other related duties as needed to help support manufacturing.
Organizational Relationships:
- The Process Engineer reports to the production manager for daily work priorities. The Process Engineer reports to the Mfg Technology Leader for technical direction and training. The Process Engineer will also work closely with the tooling staff, Manufacturing Engineers, Supervisors, Maintenance, Quality Engineers and Management. Technician staff can look to the Process Engineer for technical training and clear resolution to processing issues. The focus of communication and organizational relationships is based on technical expertise and team alignment.
Experience and/or Educational Requirements:
- Preferred 7-10 years’ experience with advanced plastic injection molding processing
- Wide range of thermoplastic material knowledge
- Knowledge on Kistler and Priamus system technologies
- Experience with 2k molding (lift and spin and rotary platen molding)
- Excellent problem-solving skills with attention to detail
- Experience in Class 7 or 8 Cleanrooms preferred.
- Understanding of ISO and FDA regulations with regard to design, process and document control, process documentations and GMP’s
- Very strong written and verbal communication, leadership, interpersonal and motivational skills
Physical Requirements:
- Must be able to work a standard 40-hour workweek with occasional overtime including weekends a possibility. Sitting and/or standing for extended periods of time as well as some walking within the facility. Must be able to see with or without corrective lenses and distinguish color differences and depth perception for product and safety issues. Hearing ability should be sufficient to hear and react to audible alarms from distances up to 100 feet. The ability to lift and carry various items up to 50 pounds.
Innovative. Trustworthy. Knowledgeable. Passionate.
Subscribe to Our Newsletter
Sign up to receive information on the latest happenings at Medbio.
#J-18808-Ljbffr
Job Tags