Suresh Patel
Process Improvement Engineer at QuVa Pharma, Inc.
- Role
- Process Improvement Engineer at Quva
- Location
- Edison, NJ, US
- LinkedIn followers
- 500 followers
About Suresh Patel
A Manufacturing Engineering / Production Engineering professional operating in the medical device industry with hands-on experience in the manufacturing process, molding, validation,product release. Collaborating with R&D engineering on disposable design and development through manufacturing technology evaluations and recommendations. All aspects of process engineering for the manufacturer of medical device components and assembly.Specialties: Strong ability to analyze manufacturing needs, including project management, and assembly and manufacturing operation sequence development. Thorough comprehension of manufacturing,machining,and insert molding procedures proven to reduce costs and improve productivity and efficiency. SKILLS:• Expert in process development, implementation, and optimization• Designing and conducting experiments, pilot and validation runs in coordination with R&D team and production personnel• Proactively identifying engineering problems and applying technical expertise and performing engineering analyses developing detailed and feasible solutions with the best approach through collaboration with colleagues• Creating documentation, train employees in the operation of new equipment, processes and SPC• Medical Device Verification and Validation Testing (Design and Process)• CAPA Investigation and Reporting, Risk Analysis (pFMEA)
Experience
Process Improvement Engineer
Apr 2021 — Present · Bloomsbury, NJ, US
Education
New Jersey Institute of Technology
Master’s Degree
Skills
- Quality Control
- Gmp
- Injection Molding
- Quality System
- V&V
- Biomedical Engineering
- Design Control
- Solidworks
- Medical Devices
- Capa
- Manufacturing Engineering
- R&D
- Manufacturing Operations
- Engineering
- Iso
- Sop
- Fda
- Lean Manufacturing
- Design for Manufacturing
- Iso 13485
- Standard Operating Procedure (Sop)
- Minitab
- Spc
- Plastics
- Validation
- Fmea
- Root Cause Analysis
- Gd&T
- Process Engineering
- Continuous Improvement
- Testing
- Product Launch
- Corrective and Preventive Action (Capa)
- Cad
- Iso Standards
- Supplier Quality
- Machining
- 5s
- U.s. Food and Drug Administration (Fda)
- Design of Experiments
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