Position description
*$500 signing bonus!**
The Process Engineer for Assembly & Packaging is responsible for leading the process, equipment, and tooling in the Assembly & Packaging areas for the Manufacturing Engineering team. The primary scope of work will be to purchase new equipment, tooling, and implement new processes in the assembly and packaging areas. The Process Engineer will work closely with validation engineers to achieve standardized methods for new and existing products, processes, tooling, and equipment for life science single use applications. This role is within the Manufacturing Engineering Team and will participate in projects in other areas of manufacturing as needs arise. Key responsibilities of this role are to work with R&D, Designers, tool room, Application Development Engineering, Manufacturing Engineering, Quality Assurance and Production to implement new equipment, tooling andprocesses into production using proper qualification and validation standards.
Key Activities:
Work independently using knowledge of current assembly and packaging designs, materials, industry requirements, and processes to drive revenue growth, cost savings, and efficiency gains that consider customer and plant requirements.
Demonstrate assembly and packaging knowledge through building prototypes, testing, and validation of the developed design for customer approval and manufacturability.
Support and/or drive productivity initiatives on assembly and packaging by working with the suppliers, procurement, and manufacturing teams.
Utilize Engineering Change Order process to direct and govern project deliverables, risk assessment oversight and analysis.
Ensure process, equipment, tooling and parts meet internal and customer requirements.
Participates and assists in process risk assessments through FMEA, part family control plans creation and updates for Assembly & Packaging areas.
Participates and assists in root cause analysis with Quality Assurance, Manufacturing Engineering and Production in customer complaints in the Assembly & Packaging areas.
In all work individual will promote a safe working environment, complies with proper use of PPE, reports incidents, and participates in functional department safety meetings. Exhibits good environmental practices and procedures consistent with job(s) performed and EMS (Environmental Management System) requirements.
REQUIRED QUALIFICATIONS
Bachelor of Science in an Engineering discipline is required
Bachelor of Science in Mechanical, Biomedical, Chemical Engineering or Technology is preferred
2-5 years of relative experience (Co-op or full time) required.
Demonstrated analytical skills, hands-on approach, proactive safety approach and sense of urgency in problem solving required.
Employee is expected to have a good work ethic, efficient and willingness to safely perform required quality work with good attendance and attitude
Familiarity with ISO, ISTA and ASTM standards is required
The employee must be proficient with a manufacturing software system (preferably QAD), accurate data entry and follow through is preferred.
Familiarity with MRP system(s) like SAP/QAD is preferred.
Experience in the medical device field preferred
Competencies of effective communications with all levels of the organization, suppliers, and customers managing multiple priorities and strong organizational skills is preferred.
Additional Requirements
Work closely with cross functional teams including customers and outside vendors to identify, plan and implement continuous improvement projects to gain efficiencies while maintaining customer agreements in Assembly & Packaging areas.
Demonstrate assembly and packaging knowledge through building prototypes, testing, and validation of the developed design for customer approval and manufacturability
Coordinate with Validation Engineers to create, plan, coordinate and execute IQ/OQ Protocols, review, analysis and summary reports for new equipment.
Determine, coordinate and execute physical package testing to ensure product and package integrity. Create, plan, coordinate and execute PQ Protocols, review, analysis and summary reports for evaluation for new process hand-off.
Maintain assembly and packaging family standards using FMEA, Control Plans, Standard Operating Procedures, Manufacturing Operating Procedures and Validated Engineering Standards to support Validation Master Plan while maintaining baselines for future quoting, part build and inclusion of new parts.
Determine, coordinate, and execute assembly testing to ensure product integrity, with focus on tubing connections. Create, plan, coordinate, and execute PQ Protocols, review, analysis, and summary reports for evaluation for new process hand-off.
Implement CapEx improvements to automate and modernize equipment, processes, material handling.
Who are we ?
Saint-Gobain's innovations touch almost every major industry around the world. Within its Life Sciences division, teams are solving critical problems for customers who are getting life-saving medical devices to the frontlines of healthcare, discovering essential medications, and nourishing and connecting the world through consumer, industrial and electronics applications. As one of the world's leading producers of high-performance polymer products, we improve lives by making simple experiences better and being there in life's critical moments.
Our team members recognize that we all create the environment for people to succeed, with a culture built on respect, open and honest communication, and honoring our commitments to our customers and each other. And at the heart of our culture, we've learned working together makes good ideas, great ones.
With a legacy dating back more than 350 years, Saint-Gobain offers employees the... For full info follow application link.
Equal Opportunity Employer of Minorities, Females, Protected Veterans, and Individual with Disabilities