Manufacturing/Process Engineer Resume Example Astrazeneca

MANUFACTURING/PROCESS ENGINEER

Summary

Contribute to the successful growth of an Organization using my skills and Experience in Manufacturing Engineer/Process Engineer to adept at completing demanding projects within crucial timeliness.

Known for analyzing a situation and quickly implementing innovative resolutions.Highly articulate Manufacturing Engineer with excellent interpersonal skills across all levels, including the effective exchange of complex technical, manufacturing and industrial data.

Highlights

Six Sigma tools expert
Root cause analysis
Project management
Operational analysis expert
Written and verbal communication skills
New product introduction (NPI)
Advanced in Microsoft OfficeChange management
Costing and yield analysis
Polymer and plastics
Change management
File/records maintenance

Accomplishments

Led new product management team that designed and developed the biggest cost saving project in company history.

Project Management

Worked directly with other departments, clients, management to decisive action.

Documentation

Wrote and edited documents to keep staff informed on policies and procedures.
Wrote the engineering chage request and preventive maintenance plansProcess Improvement

Competitive Analysis

Performed competitive analysis to make recommendations for future company growth.

Computer Proficiency

Used Microsoft Excel and Access to develop inventory tracking spreadsheets.

Process Improvement

Created new departmental procedures manual.
Assessed organizational training needs.

Protective Services

Applied safety procedures and policies as outlined in Department Safety Manual.

Experience

Manufacturing/Process EngineerMar 2009 to Current
AstraZeneca － Westborough, MA

Aseptic/BFS area) Completed small and large scale projects efficiently and timely manner.
Performed Change Request and Change Management using OCM (Operational Change Management) Platform.
Managed all calibrated instruments through PROCAL.
Worked on Deviations and CAPA's using TRACKWISE.
Worked on SAP tools for Maintenance, Work Orders, and LOTO.
Lead to Manage the Inventory in SAP and reduced the inventory cost.
Support the production of aseptic and manufacturing for RCA (Route Cause Analysis), OEE (Overall Equipment Efficiency), Lean Tools, Parts and daily activities.
Involved in QRA, 3P7, Master Validation Plan, IQ, OQ, PQ, ETP reviewing and approving through TDMS.

Maintenance LeadJan 2004 to Feb 2009
AstraZeneca － Westborough, MA

Maintenance Lead (Aseptic/BFS area) Provided crew with ongoing training and coaching to insure good manufacturing practices and safe work environment are maintained.
Maintain a clean and safe work area consistent with Quality Assurance recommendations and SOP.
Maintain all record keeping and paperwork as required by quality control, FDA and production requirements.
Maintain and Schedules all PM's and break downs repairs effectively by working with production group.
Performed Lean development task with OEE, 5S and SAP tools.
Completed CAPAs and Deviations.
Utilized Lean Manufacturing tools and improved processes to minimize waste and deviations.
Minimized and maintain parts inventory to improve cost reduction.
Performed route cause analysis to improve process and overall equipment effectiveness.
Created, confirmed and analyzed work orders, also created job aid for routine problem solving or repair actions.

Manufacturing EngineerNov 2001 to Dec 2003
AstraZeneca － Westborough, MA

Developed Lean Concept and implemented manufacturing methods and processes using Kaizen, 5S, OEE and SAP tools Worked on OEE and 5S projects and implements processes for Best effectiveness of equipment.
Performed set up for molds, temperature, air and hydraulic pressures.
Preformed IQ, OQ, and PQ on new line integration.
Assist to validate the new Blow Fill Seal processing line.
Worked with R &D, manufacturing and project engineering group for new line and product development and design concept.
Performed modification of processes and equipment for the cost reduction.
Performed verification and engineering test.
Performed route Cause Analysis by changing different parameters and SOP.
Developed an Inventory file for machine parts in Microsoft Access.
Worked in cGMP, 100 and 10,000 aseptic core areas.
Certified for aseptic gowning, electrical and SHE.

Manufacturing EngineerNov 2000 to Jun 2001
Corning Lasertron, Inc － Bedford, MA

Interface with marketing and R&D department to ease the manufacturing process and quality of product.
Performed Root Cause Analysis for Laser modules and Field failure units.
Improved process efficiency for existing product through process mapping and training existing workforce.
Support the Automated and manual assembly of modules.
Update SOP and specifications for the wire bonding and ultra sonic welding.
Performed FMEA for customer returns and introduced quality checks in the manufacturing process.
Maintained ECO documentation per ISO procedures and standards for engineering changes to support product line.

Test/Manufacturing EngineerJul 1998 to Oct 2000
Abbott Laboratories － Bedford, MA

Developed ATE and software for Blood Glucose testing monitors.
Provide support to Manufacturing, Quality Assurance as needed.
Performed modification of equipment for effectiveness and quality.
Evaluated the failure mode on production line for yield and quality.
Performed data collection and update the SPC and processes.
Preformed validation, verification and calibration equipment.
Developed and updated Manufacturing processes to improve efficiency.
Established new Test Procedures and developed test fixtures.
Performed preventive and routine maintenance of production equipment.
Supported NPI by providing vital input for DFMA.

Associate Product EngineerMar 1997 to Jun 1998
Alpha Industries, Inc － Woburn, MA

Performed Testing RF microwave components using both automated and manual methods.
Setup the equipment & calibrated for different parts.
Preventative maintenance of the test equipment.
Accumulation and review of test data to meet customer requirements.
Performed Quality test & failure analysis to formulate a corrective action plan.
Coordinated the floor activity through the supervision and daily organization of the production scheduling.
Responsible for manufacturing equipment maintenance and development.
Trained and assisted technical staffs and scheduled the workflow.

Education

Master Certificate In Lean Enterprise2015Villanova University － Naples, FL

Six Sigma Green Belt Certificate2015Villanova University － Naples, FL

Project Management Certificate2014Villanova University － Naples, FL

Lean Six Sigma Certificate2013Villanova University － Naples, FL

Certificate In Computer Science1999University Of Massachusetts － Lowell, MA

Bachelors of Engineering 1987South Gujarat University － Surat, India

Skills

Assembly, Calibration, Change Management, Coaching, Concept, Cost Reduction, Data Collection, Engineering Change Request,Product Development and Design, Documentation, Inventory, IQ, ISO, Laser, Microsoft Access, RF Microwave, Monitoring, OQ, PQ, Problem Solving, Processes, Quality, Quality Control, Quality Assurance, Record Keeping, Repairs, Risk Analysis,SAP, Scheduling, Six Sigma, SOP, SPC, Supervision, TDMS, Test Equipment, Troubleshooting ,Validation, Work flow Management.

Resume Overview

Companies Worked For:

AstraZeneca
Corning Lasertron, Inc
Abbott Laboratories
Alpha Industries, Inc

School Attended

Villanova University
University Of Massachusetts
South Gujarat University

Job Titles Held:

Manufacturing/Process Engineer
Maintenance Lead
Manufacturing Engineer
Test/Manufacturing Engineer
Associate Product Engineer

Degrees

Master Certificate In Lean Enterprise 2015
Six Sigma Green Belt Certificate 2015
Project Management Certificate 2014
Lean Six Sigma Certificate 2013
Certificate In Computer Science 1999
Bachelors of Engineering 1987

Manufacturing/Process Engineer Resume Example

Resume Score: 90%

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