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10+ years of experience
Perform functions associated with all wafer production including operations, equipment, process and training. Collects and evaluates operating data to conduct on-line equipment adjustment and ensure process optimization. Also, conduct preventive maintenance and troubleshooting.
- Saved company approximately $75K per week and $3.9M/year in downtime. Using Lean Manufacturing technique, improved throughput and operator morale by recommending standardization to the process of bringing a tool back into production.
- Completed deliverables one month ahead of schedule by managing tool installation projects.
- Received several monetary rewards for preventing potential injuries in the Fab.
- Created an Excel spreadsheet that was utilized by all shifts which led to a real time inventory, eliminated unnecessary emergency starts and resulted in a cost savings of thousands of dollars.
- Selected to be Team Lead back-up as a result of always getting the job done right and meeting output goals.
- Facilitated a new protocol for automation that when loading test wafers it puts the tool down so that tool availability could be realized and then edited the specification to reflect the change.
- As team lead of the Employee Empowerment Team, represented employees to senior management to alleviate any issues on the factory floor before they become obstacles to productivity or morale.
6-10 years of experience
Senior level equipment technician performing preventative maintenance, repair, and troubleshooting on multiple electromechanical equipment toolsets as required. Working in a team environment to prioritize, schedule and complete own work as well as direct the work of junior level technicians. Use equipment and process knowledge to meet the production goals of the organization.
- Contributed to safety and efficiency of all scheduled preventative maintenance tasks by editing checklists and adding visual job aids to the currently used specifications. Equipment availability increased by 2%.
- Decreased a scheduled pm from over 48 hours to less than 32 hours by standardizing maintenance practices across all shifts, as a member of the High Performance Maintenance team. Equipment availability increased by 3%.
- Installed a hardware and software interlock on the elevator process chilled water loop. The interlock was successfully installed on 29 machines preventing a wafer mis-processing situation from occurring again.
- Increased shift’s overall effectiveness by leveraging instructional and time management skills to deliver peer training to multiple team members.
- Rebuild spare parts and test for functionality for upcoming preventative maintenance activities.
6-10 years of experience
Appointed manufacturing lead within first year.
- Recognized as the lamination expert within company.
- Developed semi automated process to apply Anti Reflective laminate film to LCD’s
- Increase Coating machine throughput by changing substrate size and coat machine tooling.
- Improved cleaning and preparation methods of plastic substrate prior to coating resulting in higher throughput and yields.
- Managed production floor priories, coordinated work of part through different segments of company to insure quality and adherence to schedule.
0-5 years of experience
Familiarity with process of clean room gowning and working within a clean room Fab.
- 3 years’ experience in Dielectrics (LKL, CDO, CDT) Copper and Non-copper.
- Performs Scheduled/Unscheduled PM’s, tool qualifications, and Engineering gameplans for troubleshooting
- Reads/Reviews data through SPC, Klarity, E3, REV, QEF
- Performed set-up, calibration, and preventative maintenance on production equipment
- Created Logbook entries, conducted daily shift passdowns
- Lead maintenance technician, supervised personnel on equipment maintenance, completed all tool maintenance certifications
- Successfully maintained the highest standards of expectations through one technology and helped successfully startup new current technology, showing the capability of a successful learning and performing trait in a very fast, intense environment.
- Received Exceeds Expectations and Paygrade promotion within first year evaluation of semiconductor industry.
0-5 years of experience
Supported projects such as line extensions, manufacturing, and process improvements for a wide variety of surgical instruments in a very fast paced environment. Performed numerous clinical-use testing for validations and investigations.
- Lead technician responsible for supporting 298 unique products including project launches, manufacturing optimization, line extensions, and solving manufacturing challenges.
- Lead technician in the successful qualification of third party supplier/vendor transfer in order to increase quality of two product lines.
- Lead support in arthroscopic wand product launch to increase revenue by $500K/yr.
- Performed clinical-use and integrity testing for validations and investigations regarding Laparoscopic Scissors, Arthroscopic Shavers, Blades and Biopsy Forceps.
- Provided technical consultation from production perspective to cross functional team.
- Directly supported expansion of Arthroscopic Shaver line to launch Ambulatory Surgical Center makert growth initiative; opening more than $500K in potential revenue.
- Investigated CAPA and customer complaints by performing failure analysis leading to validations.
- Trained managers, supervisors and technicians on testing equipment, approved process design changes and safety compliance in the workplace.
6-10 years of experience
Responsible for the daily operations of dry etch machines, output and quality. Served as area Team Lead between manufacturing and management.
- Consistently meet all quality expectations annually, thereby contributing to the overall achievement of the team output goals.
- Lead area team meetings, assign action items, and ensure all are completed in a timely manner.
- Worked as part of a cross-functional team to create a safe working environment by revamping the site’s hazardous energies and standards.
- Served on the Emergency Response Team as Logistics Officer.
- Collaborated with Engineering and Field Service to standardize maintenance procedures and specification edits.
- Identified as a key member of a team to compare site lean safety quality across several Intel manufacturing facilities.
- Recognized for individual achievement as member of special team tasked with decommissioning and converting toolsets. Completed all tasks with safety and quality in mind while turning the tools over in an accelerated schedule, reducing timeframe from 40 to 20 days.
- Received multiple financial awards for quality job performance, safety, and team work.
0-5 years of experience
Multi-task through Litho and PDPI areas in Fab 32 and Fab22 working with 12″ silicon wafers in a clean room environment. I perform a variety of routine operations supporting wafer fabrication in these specific functional areas.
- Primary work duties include minor preventive maintenance, troubleshooting, non-standard processing and problem-solving.
- Maintained chemical levels and quals while following safety policies and procedures.
- Implement tasks for the Engineers and IQ group members such as protocol audits; placing plastic kits around all EMO buttons on all newly installed tools; making sure all proper paper work is bundled in plastic sleeve jackets for the install process; creating and laminating signs for all tool owners; and, ensuring all necessary assignments are fully completed in a certain time frame.
- Oversaw equipment maintenance as an Acid Buddy for Wet Etch Manufacturing Techs in Fab32 and Fab22.
- Organized and cleaned designated areas in the sub-fab and basement.
- Delegate and adjust Epi lots in the Hydrogen Oxygen Purge area.
0-5 years of experience
Operational knowledge of manufacturing equipment and performing multiple test, automated and manual on various fuel injectors parts, components, subassemblies and final assemblies and analyze, interprets and document collected data
- Performs numerous time-sensitive projects while multi-tasking to ensure timely delivery of quality assured product
- Interacts and collaborated with internal customer to understand their needs
- Ensures compliance to ISO audit requirements
- Reviewed and updated manufacturing test data through manufacturing database before submitting
- Knowledgeable in carefully handling different types of fuel
- Collaborated in improving and sustaining of the facility that resulted in scoring 100% in 5S Kaizen
0-5 years of experience
Manufactured pharmaceutical CGM device for non-clinical, pre-clinical and clinical studies using cGMP / GLP method
- Supported activities in process and product development
- Executed manufacturing processes for the given area with strict adherence to cGMPs regulations and guidelines and established practices and safety procedures
- Assisted in troubleshooting of equipment and process issues
- Train less experienced or new colleagues
- Author new procedures as well as revise current procedures
- Uses independent judgment and initiative to continuously improve the quality of manufactured product and efficiency of manufacturing operations
0-5 years of experience
Performed electromechanical and electrical troubleshooting; Inspected machinery and calibrated, alignments and repairs
- Configured and updated software applications and completed installations
- Conducted testing on circuit boards, pumps, tubes and all other parts
- Identified and repaired malfunctioning components such as replacing harness wires
- Recorded data accurately and completed thorough documentation
0-5 years of experience
Performed a plethora of manufacturing duties for an automotive company servicing General Motors, Ford, and Chrysler including running vertical presses; producing spindles and extruding tubes; assembled independent drive shafts; operated waste treatment and acid wash department
- Inspected parts as they came off line; Inspected equipment to ensure it met safety and operational standards
- Organized line team; ensured that all members were at their designated location; notified management of absences
- Met or exceeded daily quotas for part production
10+ years of experience
Handled the tasks of monitoring and supervising production policies and activities to ensure compliance with guidelines of quality control
- Responsible for checking the quality and production specification of materials delivered by suppliers
- Performed weekly the quality audit for over 2 million direct mail products
- Ensured that quality assurance inspections are completed according with the company standards
- Assigned the tasks of documenting conducted tests on the production line
- Prepared and presented to supervisors quality assurance reports and implemented corrective measures to minimize quality defects
- Investigated material shortages and material quality issues and presented outcome to supervisors
- Archived and maintained quality assurance samples in accordance with company regulation and Sarbanes – Oxley requirements
- Worked with customer service group and shipped samples to customers
10+ years of experience
Performed numerous tasks in multiple areas of the factory that produces semiconductor material that creates computer chips. Served as a manufacturing operator/maintenance technician on various semiconductor equipment performing basic Preventative Maintenance and troubleshooting with great attention to detail and quality.
- Served as a Remote Operations Center (ROC) monitored and processed product through multiple tools in numerous areas and kept close communication with floor technicians, engineers, and management to ensure product is processed through the factory quickly with an emphasis on quality.
- Participated in development projects with engineers to improve performance, quality, and overall factory efficiency.
- Trained employees to perform normal factory operations at a highly efficient level.
- Demonstrated leadership qualities in embracing new manufacturing technologies and methods introduced by management and getting buy in from peers to do the same.
0-5 years of experience
Prepared the production by thoroughly following MBR documents and the production schedule, clarifying process specifications, calculating, weighing, blending, granulating, and milling raw materials
- Prepared and cleaned equipment and rooms by performing Major Clean/Minor Clean following the checklists and SOPs
- Maintained safe and clean work environment by following cGMP and SOPs, complying with legal regulations
- Documented production by completing forms, batch records, rooms and equipment log books
- Updated job knowledge by participating in training opportunities
0-5 years of experience
Manufacturing Driveshafts as Tier 1 Supplier for GM and axles for Ford, Honda, Nissan using CNC Machining
- Gauging to Microns level, coordinated quality checks, high production levels
- Critical Path methods, ISO Certified and Safety methods utilized for Environmentally safe manufacturing
- Trained and developed new Team members
- Just in Time Delivery based on pull system
10+ years of experience
Exceptional attention to details when operating and running tools.
- Worked in a clean-room environment where I’d have to wear surgical style gloves to handle any materials. This was a class 100, top of the line clean room with laminar airflow.
- Used variety of hand tools including screw drivers and torque drivers.
- Ensured area was coordinated correctly to maximize safety.
- Worked in CVD, TF Metals, Implant, Diffusion, Etch and E-Test
- Trained on preventive maintenance on the Implant tools, CVD and most recently AMAT Endura PM’s.
0-5 years of experience
- Performed manufacturing activities related to Dispensing raw materials, Spray drying, Capsule filling, and Packaging in order to produce a commercially sold pharmaceutical product.
- Manufacturing activities also included the cleaning, maintaining, assembling, operating, and trouble-shooting of processing equipment.
- Performed and ensured that all issued materials were transacted in SAP.
- Performed HSE monthly audits.
- Collected and maintained data on operations performed.
- Independently initiated and executed Protocols related to equipment changes and upgrades.
0-5 years of experience
Responsible for achieving production requirements.
- Made sure that products were produced on time and are of good quality.
- Removed rough spots from work pieces with portable grinders, hand files and scrapers.
- Detected faulty operation of equipment and defective materials and promptly resolved issues.
- Recognized and reported defective material and equipment to shift supervisor.
- Verified part numbers and placed parts in appropriate shipping containers.
- Observed all safety policies and procedures.
6-10 years of experience
Facilitated a high degree on cleanliness on wafer handling containers insuring timely production deadlines and quotas as specified by management.
- Improved production and maintenance procedures by collaborating with Engineers.
- Assisted in other module areas including parts cleaning, wafers in process coordinator, and equipment.
- Reported variance analysis to direct superintendent.
- Assisted in training of new employees.
10+ years of experience
- Certified in component insertion, Glue, High Pressure Wash, Quality Control Testing and Post Analysis. Manual Microscope Inspection and assembly of Microfluidic Chips.
- Worked with engineering closely and was involved in multiple Improvement Teams.
- Revised Standard Operating Procedures to support manufacturing operations.
- Mentored and trained new hire operators.
10+ years of experience
Certified in all manufacturing steps from Front-End to Back-End of company’s microfluidic chips including, Lithography, Wet Etch, Bonding, Inspection, Dicing, Gluing and Packaging.
- Responsible for training and certifying new technicians per company’s SOP’s.
- Performed visual inspection of product under manual microscope as well operating automated inspection systems.
- Working with manufacturing improvement teams updated and improved SOP’s as well as validating new processes and equipment.
- Performed QC testing of product which involved mixing and pipetting of samples and reagents
- Performed entry of manufacturing process data into computerized system i.e. Camstar’s MES.
0-5 years of experience
Assisted Group Leader with the completion of work orders and adhering to a strict schedule.
- Assisted in maintenance and calibration of test equipment and benches.
- Assisted fellow technicians in troubleshooting and repair of x-ray machines.
- Cross trained on three different product lines, as well as provided on job training to fellow technicians as needed.
- Responsible for all functions listed below.
0-5 years of experience
Initiated, reviewed, and reconciled batch records to ensure quality.
- Performed and trained personnel to provide environmental monitoring for employees.
- Setup and adjusted equipment for operation in a class 100 grade A environment.
- Operated TL8 filler, west capper, tray loader, and vial washer according to SOP’s.
- Ensured environmental integrity of work area and production equipment was being met.
- Maintained batch board’s consistency per process to ensure production goals were being met.
- Received, checked, stored, and handled drug products as required and/or directed.
- Maintained and reviewed logbooks to ensure requirements for production were being met.
0-5 years of experience
- Performed mass formulations of buffers, reagents, and diluents to fulfill customer orders and for in-house use.
- Implemented and edited Standard Operating Procedures (SOP) and examined them for inconsistencies.
- Maintained laboratory equipment and laboratory space
- Coordinated product transfers from the Bulk Reagent Manufacturing department to other departments.
0-5 years of experience
Conducted all aspects of manufacturing for pathogen detection test kits utilizing isothermal nucleic acid amplification technology.
- Performed in-process quality control, and worked independently to solve problems as they were found.
- Operated and maintained robotic dispensing equipment.
- Member of Safety Committee, helping to ensure that the building remained safe for all coworkers.
- Prepared and improved manufacturing work instructions for relevant standard processes.
- Recordkeeping and inventory for all manufacturing processes.
0-5 years of experience
Weighs and samples research and clinical manufacturing batches in accordance with applicable SOPs.
- Operate manufacturing equipment such as Xcelodose and MG2 encapsulators, Fette tablet press, and Glatt fluid bed processor
- Set up, operates, breaks down and cleans equipment to be used in manufacturing research and clinical batches
- Performs scheduled manufacturing activities in accordance with approved batch records
- Supports the Manufacturing and R&D departments by moving all raw materials and finished goods from the Warehouse to the Manufacturing area for production and storage
10+ years of experience
Supported daily operations, Engineering, PM Maintenance, along with troubleshooting maintenance issues.
- Operator and Equipment Repair and Troubleshooting Certification on Multiple ETCH, PLANAR, Spartan Sorter\SMS and Grinder\Mounter toolset. Proficient troubleshooting vacuum, pneumatic, interlock, slurry, RF and water cooling systems for deposition, uniformity control and chamber cleans.
- Worked with specifications and checklist to ensure work is in compliance and replace items that fail, includes written and visual inspections.
- Excellent Team facilitation and ISO Auditor. Instructed and trained all team members.
- Advanced Peer Trainer 2, trained all staff levels in operations, this included tool and fab specific skills at the highest level.
- Area Coordinator, adapted to everyday conditions of tools, personal and product demands that consistently changed.
- Calibration Coordinator, track tools for calibration and repair.
- Trained in Lean Manufacturing process. Applied process to production floor and maintenance work areas.
10+ years of experience
Shift team leader- responsible for the help of others and daily operations
- Certified/designated trainer- trained and assisted over 30 operators with numerous aspect of crystal growth process.
- Responsibilities included running equipment, decision making, documentation, data entry
- Worked with engineers to help implement, improve and troubleshoot procedures
- Managed the daily report on the status of equipment, ordering of supplies and inventory control
- Provided customer service explaining the process and development
0-5 years of experience
Prepared equipment to run manufacturing processes
- Monitored and adjusted production processes and equipment to ensure quality
- Prepared, assembled and loaded manufacturing materials
- Calibrated and adjusted equipment to meet optimum quality levels
- Maintained production logs and prepared documents
- Initialized and shut down processing equipment
- Troubleshoot equipment problems and install new hardware
0-5 years of experience
Ensure the effective and appropriate processing of wafers through changing temperatures and adjusting recipe settings.
- Assist L2P by using SPC chart to monitor the product/layer parameters and AIS/Moving range values.
- Supporting continuous improvement activities for productivity and yield enhancement.
- Interfacing and passing down information with incoming and outgoing shifts.
- Maintaining optimum performance of equipment through scheduled preventive maintenance and Calibration of equipment (dailies).
- Performed BKM’s and RFC’s to resolve maintenance issues to improve equipment reliability and minimize equipment downtime.
6-10 years of experience
Tested system for LitePoint Co. products as Pebble Beach IQ 2011, IQ 2012, IQ 2015, IQ NAV, IQ Flex BG, IQ View, IQ X Stream
- Tested electronic components, digitals boards and memories after Burn-In Chamber
- Completed configuration, certification, and wi-fi tests, Evm, Diagnostic, IQ signal, Lock Flask Drive, FM, GPS, Hipot, Ground test, Burn-in test
- Tested system DDN 4600 in Drive Dual JBOD for Newisy company
- Test Technician/Assembly Technician for Ciena Online Metro Network Co. and Opnext Co.: Calibration Zx1 Mini Intefeometer Dorc Test PMS 6.11
- Operated, set up, and oversaw maintenance of SII OFL-15 Seiko Fiber Optic Polisher machine
10+ years of experience
Manufacturing process.
- Duties include: operation of various equipment, maintaining and training of Semi Conductor Incorporated (SSI) developer and coater, SVG coater and developer, and Takatori Laminator.
- Certified in Positive, Negative, Print / Solder Dep and Descum / Plasma Etch processes.
- Duties in Plasma Etch also include: Operating Gassonics International, Cheetah 200 and Matrix system 10.
- Equipment set up and troubleshooting, trained peers on quality criteria.
- Certified in Ultrafab Stripper, Sikama and Heller 1700 EXL ovens, HTI, Dek solder printers, and EO backside laser mark.
- Knowledge of SPC (Statistical process Control) and ISO 9000/9002 Methods. Perform daily and weekly PMs.
0-5 years of experience
Built and tested GeneXpert I, II, IV, and XVI systems using GMP, SOP’s and Agile systems.
- The GeneXpert Dx System automates and integrates sample preparation, nucleic acid amplification, and detection of the target sequence in simple or complex samples using real-time Polymerase Chain Reaction (PCR). The system is suited for in vitro diagnostic and research based applications that require hands-off processing of patient samples (specimens) and provides both summarized and detailed test results data in tabular and graphic formats. The GeneXpert system can only be used with the GeneXpert cartridge.
- Processing chambers-Hold samples, reagents, processed sample, and waste solutions. One chamber is designated as an air chamber to equilibrate pressures within the cartridge.
- Valve body-Rotates and allows fluid to move to different cartridge chambers and to the reaction tube. Within the valve body, the specimen is isolated, PCR inhibitors are removed, and specimens are ultrasonically lysed (if applicable). After the sample is processed, it is mixed with PCR reagents and moved into the integrated reaction tube.
- Reaction tube-Enables rapid thermal cycling and optical excitation and detection of the tube contents. The reaction tube is automatically inserted into the I-CORE module after the cartridge is loaded into the instrument.
- Built and tested smartcyclers, automated real-time PCR system. Available in 16, 32, 48, 64, 80, or 96 site configurations. Up to 96 different cycling protocols can be performed simultaneously in one system. Multiple experimental runs can be started at different times, allowing several operators to use the system concurrently.
0-5 years of experience
First employee of a multi-million dollar medical tape converting business venture, built from the ground up with a company that had no prior experience in tape converting.
- Implemented and engineered manufacturing processes for multiple FDA regulated applications and parts used on human skin in a medical environment, creating many parts for the first time.
- Researched, developed, and created production processes for every part in production.
- Created all document templates and processes including Standard Manufacturing Procedures, Operating Procedures, Quality Control standards, training manuals, FDA record sheets, job setup sheets Trained multiple new machine operators, some with no prior converting experience.
- Sourced vendors for every aspect of the business, from raw material vendors to packaging.
- Logged, trafficked and updated projects in job management software.
- Created project job jackets, including briefs, schedules, reference material, specifications and contractual requirements.
- Adjusted press during production runs to maintain specific registration and color densities.
- Scheduled preventive maintenance for book block equipment.
- Produced high quality finished printed material in a timely and efficient manner.
- Led project kickoff meetings and oversaw project scope assessments.
0-5 years of experience
Responsible for a wide variety of duties associated with the manufacturing, clinical and commercial products
- Collected and evaluated operating data to conduct on-line adjustments on products, instruments, and equipments
- Assembled standard operations equipment such as mills, presses, and encapsulator
- Operated a variety of production equipment, including granulators, blenders, and presses
- Weight, measured, and checked raw materials to ensure product manufacturing contains proper components, ingredients, and quantities required
- Maintained records and manufacturing environment to comply with regulatory requirements, current Good Manufacturing Practices (GMP’s) and Standard Operating Procedures (SOP’s) complies with all applicable safety requirements
- Maintained tooling inventory
- Performed in-process testing to ensure batches meet specifications
- Followed safe working practices while performing assigned duties
- Lifted and moved up to 25 pounds
0-5 years of experience
Assist in manufacturing of Glycated Serum Protein Assay Reagents, Controls, and Calibrators.
- Perform in-process testing for Direct HbA1c Assay and Liquid GSP Assay to assure batches meet specifications in terms of control recoveries, activity, and linearity.
- Perform research to improve the Assay’s Performance.
- Have good experience with making blood lysate for the HbA1c Assay testing.
- Have good experience with performing Dialysis.
- Perform filling, labeling, and packaging of finished products to prepare them for shipments.
- Maintain records to comply with regulatory requirements, GMP’s and standard operating procedures.
0-5 years of experience
Part of the Continuous Improvement Program
- Compiled data in order to create flow time analysis and cycle time
- Daily meeting with supervisors and lead techs in order to improve data
- Assistance in product line strategic projects through analysis and implementation of new methods
- Ensured work orders were input into the system
- Assisted assemblers in correcting work orders and helped correct
- Assisted the assembly crew by answering questions and explaining
- Trained assembly workers on basic data entry
0-5 years of experience
Operate, maintain and troubleshoot Novellus Vector toolsets for the manufacturing of 22 nanometer wafer production.
- Process and maintenance knowledge of Carbide, Nitride, and Oxide tool flavors in the dielectric process and wafer cure process.
- Responsible for 12 toolsets ensuring proper processing of wafers and all preventive maintenance procedures.
- Routinely open tool compartments for preventive cleaning and replacing of used parts.
- Direct contact for processing engineer to perform technician tasks on the operational level.
- Broad knowledge from wafer manufacturing to toolset processing.
- Interpet graphs and charts along with metrology test tools to ensure toolsets are operating within specified target areas.
6-10 years of experience
Perform preventative maintenance and repairs on all manufacturing test equipment and fixtures.
- Participates in Continuous Process Improvement teams.
- Well organized and able to multitask.
- Perform test and repairs.
- Assist engineers on product verification testing and reported results to engineering.
- Perform evaluations on new software revisions for manufacturing test systems
0-5 years of experience
Operate general manufacturing equipment in accordance with current GMP’s or standardized procedures and within safety guidelines as well as large scale bioreactor operations, critical small or large volume sterile fills, and aseptic manipulation of cell cultures.
- Operates with minimal supervision complex systems and equipment and optimizes their use in accordance with defined goals.
- Assisted in the implementation of production procedures to optimize manufacturing processes.
- Participated in authoring complex, explicit documentation for manufacturing operations.
0-5 years of experience
Operated machines such as Fabricator and Poucher for the production.
- Trained new associates to run and troubleshoot the machine when needed.
- Performed AQL Inspection and categorized defects for rejection.
- Maintained accurate batch record documentation, performed scale/balance weight checks.
- Adhered to cGMPs and SOPs, safety guidelines and procedures.
- Maintained equipment and work areas in a clean condition and packaged finished products into cartons, and boxes.
0-5 years of experience
Assisted in all aspects of product manufacturing for Smart Energy consumer electronics manufacturer
- Assembled and tested product for final sale to customer
- Programmed and reworked circuit boards in effort to keep all products up to date
- Packaged, shipped and tracked customer orders
- Tracked inventory of raw materials used to build final product
0-5 years of experience
Control cabinet manufacturing and wiring
- Adept at reading all wiring schematics, T3000, E3000 and special voith cabinet
- Skilled at identifying problems and implementing solutions
- Successful site equipment update and test for Progress Energy, Florida, May 2013
- Mechanical and electrical assembly
- Read blueprints
- Lean training, power tool training and lockout/tagout training
0-5 years of experience
Ability to troubleshoot any problems with machines
- Work safely in a manufacturing environment
- Identify and segregate product according to quality standards
- Perform quality assurance checks accordingly through jobs
- Learned all machines in BCF area (4 machines, and 2nd and 3rd floor)
- I performed as a miscellaneous operator (ability to run anything in plant)
- Ability to read and follow SOC and SOP accordingly
0-5 years of experience
Working closely with engineers to set up test area and move from research and development to high volume manufacturing area.
- Perform operation of Pilot and/or Production equipment
- Perform Preventive Maintenance for equipment related to process ownership per required specifications
- Check wafers for damage, discolorations, delaminations, Etc.
- Collecting data from sample cells for Engineering after going thru extensive tests.
- Taking bus bar thickness measurements using Dektak machine.
- Final cells inspection and Packaging.
0-5 years of experience
Handle incoming and outgoing shipments of raw materials, solutions, and equipment; track status of requests and communicate with customers
- Draft daily and weekly progress reports, deliver updates of projects and production, draft documents for process changes and service level agreements
- Utilize Microsoft Office Suite, Ultriva, Google Drive, gMail, and SAP computer systems to perform
- Communicate effectively with team and other groups in a fast paced FDA regulated cGMP environment
- Review and revise manufacturing documents by following Good Documentation Practices (GDP) for quality assurance
- Participate in process improvement projects and emergency response teams
0-5 years of experience
Work closely with team of assembly personal, technicians, and QC to manufacture a first-of-its-kind medical device
- Perform in process quality checks and report any suspected problem
- Maintain controlled environment room integrity using proper attire and adherence to CER practice and procedures
- Maintain accurate records and documentation related to quality, work in process, test results, work times, and special projects
- Adhere to general safety rules, manufacturing procedures, company policies and procedures, QMS and regulations
- Recommend, initiate, or provide solutions to design and process issues
0-5 years of experience
Set up sensor management computer with Linux filesystems for all commercial vehicles using Ubuntu
- Test satellite comms, function/calibration for sensors such as wave-height sensors, Acoustic Doppler Current Profilers, Hydrocarbon sensors, Magnetometers, Sonardyne Acoustic modems, Water temperature/salinity/depth, and Fluorometers.
- Writing detailed Manufacturing Process Instructions for setting up the sensor management computer.
- Extensive work with Arena (product lifecycle management that unifies organizations and their supply chains around a centralized bill of materials)
- Creating part/assembly drawings using Solidworks, and creating the corresponding Bill of materials.
- Assembling the hand-built Wave-glider from start to finish.
0-5 years of experience
Supervise activities of 9-member team to manufacture medical blood devices following TMP procedures and GMP protocols.
- Manage validation projects to meet product release requirements and timelines.
- Prepare line for manufacturing runs based on production needs; troubleshoot and maintain equipment.
- Maintain production quality standards in highly stressful manufacturing environment.
- Identify process or product non-conformance and promptly alert engineering and technical staff.
- Assign tasks and provide performance coaching; rotate team members through each station to prepare for other line assignments; trained over 20 new operators to date.
- Participate in continuous improvement initiatives; provide regular production reports to Shift Supervisor.
- Promoted from Operator and Technician within first 5 months.
0-5 years of experience
- Contract pharmaceutical manufacturing in a cGMP environment
- Cell culture manufacturing with 20L, 150L, and 800L fermenters
- Adherence to batch records, SOPs, process schedules
- Performed inoculation, induction, harvest, lysis, and fill stages
- Instituted a small parts inventory system for product changeover procedures
- Proficient in the use of fermenters, centrifuges, homogenizers, and bench-top eqp.
Manufacturing Technician Education and Certification
While higher education is not required to obtain employment as a Manufacturing Technician, some candidates have either Bachelor’s or Associate’s degrees in Engineering or a related field. These candidates are usually looking at the role of Manufacturing Technician as a stepping stone to reach higher positions within the manufacturing industry. The more common educational route for Manufacturing Technicians is to earn a certificate from a vocational school. Vocational programs often have built-in apprenticeships that provide students with the skills they need to succeed in the job market. Apprenticeships typically last 1-2 years, and on-the-job training can be anywhere from 1 to 3 months. An example of one such program is that of
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Manufacturing Technician
Last edited by: Gabriela Barcenas, CPRW, Content Writer II -
Gabriela Barcenas
CPRW, Content Writer IIGabriela is a Certified Professional Resume Writer (CPRW) and career adviser. With 10 years of digital media experience and five years of resume writing expertise, her publication history includes fashion, education, travel, social justice, equitable design and career advice.
