BIJAN DADOLAHI SARAB

** ******** **** ****• AJAX, ON• L1Z 1R1• 416• 857• 7004

•Email: adn6b9@r.postjobfree.com •LinkedIn: ca.linkedin.com/in/bijandadolahi

Biomedical Engineer/ Hardware Engineer

A solution-focused and accomplished Engineer adept at driving development and improvement of manufacturing processes. Extensive experience working on highly regulated industries such as Medical Devices. Possess unique blend of technical acumen, resource management abilities, and high-level project management skills—especially as they pertain to medical device development. Adept at communicating directly and professionally with senior management regarding project status updates and reviews as well as developing standard processes and tools to ensure uniformity of deliverables across all projects.

CORE ATTRIBUTES

Primary Competencies Knowledge Areas Technical Skills

• New Product Introduction (NPI) • Control Systems • Assembly Language

• Lean & Six Sigma • Microprocessor Systems • C Language

• Process Validation, Design Transfers • Biomedical Instrumentation • Coventor

• Problem Solving and RCA • Technical &Professional • MATLAB

• MFG Continues Improvement • DFM, PFMEA, PLM • Java

• System Integration and Installation •Biomedical Signal Processing • LabVIEW

• Engineering change order • Digital System • Python

• S.O.P and ISO13485 • AutoCAD/ SolidWorks/ Inventor/Master CAM

• Medical Device R&D

EDUCATION

B. Eng. Biomedical Engineering Ryerson University — Toronto, ON April 2014

B. Eng. Agricultural Engineering Azad University — Iran, Kerman June 1994

CNC Master CAM- Toronto Metro College – Toronto, ON Jun2020- present

PROFESSIONAL EXPERIENCES

Manufacturing Engineer Conavi Medical Inc. – Toronto, ON Jan 2019 – Mar 2020

•Evaluated and developed new manufacturing processes by analyzing production data from quality control.

•Developed and monitored MFG process by NCR data analysis (Pareto chart).

•Collaborated with suppliers of outsourced parts, assemblies and products to resolve quality or supplier issues.

•Actively participated in the investigation and resolution for Corrective Action and Preventative Action (CAPA).

•Guided junior colleagues including interns on principles of manufacturing process engineering and design for manufacturability (DFM).

•Developed, implemented, and transferred of MFG process, Tools and materials for new product introductions (Intra-Cardiac Echo “ICE PIM”).

•Stabilised the continuous improvement on MFG process of intravascular ultrasound system (IVUS).

•Developed ECN to update MFG work instructions, tools and process

• Developed investigation plan, RCA and risk analysis to prepare the rework instruction for NCR, RMA and customer feedbacks.

•Worked close by R&D team during prototype phase and collaborated with DFMEA.

•Familiarised /Trained with clean room rules and regulation through SOP

Manufacturing Engineer Synaptive Medical Inc. – Toronto, ON Oct 2014 – Dec2018

•Evaluated, established, improved, and qualified manufacturing processes following GMP and Medical industry guidelines.

•Developed, implemented, and transferred of manufacturing processes and procedures for new product introductions (Solais) and continuous manufacturing improvement opportunities.

•Supported the Production Team by technical troubleshooting efforts related to electromechanical systems, computer systems, and imaging systems.

Developed, built, and qualified manufacturing testing stations including hardware and software installations, assembly test fixtures/jigs, and other test equipment as required.

•Conducted training and provided guidance and supervision for Production Technicians on assembling, testing, troubleshooting, and repair techniques of electromechanical equipment.

•Improved manufacturing efficiency by analyzing and planning workflow, space requirements, PFMEA/DFMEA/DFM and equipment layout while meeting manufacturing process, product, and quality assurance requirements.

•Provided inputs to the product development staff for continuous improvement initiatives for product manufacturability and serviceability.

•Developed and updated manufacturing work instructions, device master records, and other documentation as required and implement approved changes through ECO process.

•Assured product and process quality by designing testing methods and establishing standards to confirm manufacturing process capabilities. Provided manufacturing decision-making information and communicate production status, deviations, issues and general information to manufacturing management.

•Assisted during internal/external audit process.

•Certified on FARO, Laser Safety Officer, IPC/WHMA-A-620 and Lean( 5S,7Wast, Kaizen and process control)

•Registered and received EIT number as an Engineer Intern from PEO.

•Canadian Citizen with valid drivers licence

Automation Technician Roni Excavating — Concord, ON 2007 – 2008

•Repaired a variety of heavy duty machines mostly Hydraulic and Pneumatics problems for this provider of heavy equipment and excavators serving industrial, commercial, and residential clients.

•Provided well-informed recommendations and decisions pertaining to the effective restoration of equipment, ultimately reducing downtime during equipment failures.

Tester and Debugger M.I.S. Electronics — Richmond Hill, ON 2006 – 2007

•Familiarized and worked with MRP system “Sys-pro”.

•Managed shipping and receiving department as well as handling of testing and inspection of electronic boards and components.

•Tested and debugged electronic boards designed in medical equipment and components prior to distribution to the company’s reputable clients; Negotiated discounted pricing of electrical components with vendors and assessed the bills of material (BOM).

Quality Assurance Specialist Vecture Electronics Inc. — Concord, ON 2005- 2006

•Examined electronic boards for damages and inconsistencies at this original manufacturing and engineering firm specializing in electronics system design.

In-Circuit Test Debugger Intl. Celestica Inc.—Toronto, ON 2003 – 2005

•Debugged computers and electrical issues related to circuit boards under stringent deadlines within a high-pressure environment.

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