Revvity Inc., Greenville SC is seeking a Mechanical Process Engineer with a focus on process and product sustainability. Ideal applicants should have a thorough working knowledge of medical device quality systems. A strong background in mechanical systems, mechanical design (using CAD), and product optimization using Six Sigma methodologies across multiple cells with experience in manufacturing environments.
ESSENTIAL ACCOUNTABILITIES:
Managing quality noncompliance with sustainable root cause and corrective actions.
Participates in the design and development of mechanical and electro-mechanical systems.
Manages manufacturing processes and documentation, plus supports design engineers on BOMs, drawings, routes, and prototyping assemblies.
Plans, coordinates, and optimizes all plant lean initiatives by continuing to support internal Gemba, MUDA, Kaizen, Time Studies, and Work Cell layouts methodologies.
Support all technical services with other process engineers and coach junior technicians to maintain a high level of customer support.
Confers with vendors and engineers’ best practices to ensure product design and tooling to boost production efficiencies.
Analyzes and captures data to decipher tests, troubleshoots, and provides solutions to technical problems with preventative measures.
Strong statistical data analysis and SPC for optimizing product reliability.
Works cohesively with the staff on all material quality constraints (MRBs) to ensure actions and root cause are actioned immediately and dispositioned accordingly.
Evaluates and optimizes space requirements, cell workflow, materials constraint, design, and equipment layout for maximum efficiency.
Formulate long and short-range strategies for continuous improvement of processes and equipment needs.
Implement Six Sigma methodologies to reduce cost and waste by using MUDA or Kaizen improvement best practices.
Experience and understanding of PFMEA, FMEA, DMAIC Process.
Able to maintain a high level of professionalism and enhance a team environment culture that motivates the Omni production workforce.
Mentor, motivate and lead full-time and staffing associates.
BASIC QUALIFICATIONS:
OR
PREFERRED QUALIFICATIONS
Experience with a Class 1 Medical Device Manufacturing
CAD design of mechanical systems in SolidWorks (v2014 or newer) and Composer (3D Modeling)
Experience with MS Office software products
Ability to translate client requests into existing systems at optimal cost and time targets.
Have a strong sense of urgency.
Must be a motivated self-starter with the ability to work independently.
Maintain a positive work atmosphere by behaving and communicating in a manner that gets along with customers, clients, co-workers, and supervisors.
Must be a team player with a strong customer orientation.
Understanding of electronic document control systems (PDM).
Experience in a design and manufacturing environment certified to ISO 9001/13485.
ERP/MRP systems for data gathering and reporting
Knowledge of PLC, Robotics, Programming, and machine shop fabrication helpful.
PHYSICAL JOB REQUIREMENTS:
Sitting, standing, and bending
Lifting and/or moving up to 40 lbs.
Regularly required to use hands to finger, handle or feel, reach with hands and arms, and talk or hear
Specific vision abilities required for this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust and focus.
- Office and warehouse environment
SAFETY:
Adhere to company safety policies and procedures
Wear required PPE (personal protective equipment) where needed
Immediately report any unsafe conditions or other safety-related issues
SHIFT/SCHEDULE:
Standard 1st Shift hours are 07:30 am – 04:30 pm Monday through Friday. Flexibility to support additional hours/overtime as required to complete the duties of the position / based on the production schedule.
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