Top Manufacturing Associate Skills

Below we've compiled a list of the most important skills for a Manufacturing Associate. We ranked the top skills based on the percentage of Manufacturing Associate resumes they appeared on. For example, 11.2% of Manufacturing Associate resumes contained Safety Procedures as a skill. Let's find out what skills a Manufacturing Associate actually needs in order to be successful in the workplace.

The six most common skills found on Manufacturing Associate resumes in 2020. Read below to see the full list.

1. Safety Procedures

high Demand
Here's how Safety Procedures is used in Manufacturing Associate jobs:
  • Write work Instructions/job hazard analysis to improve the operating functions at each workstation and to improve quality/safety procedures.
  • Observed safety procedures around multiple hazardous machinery resulting in no lost time or machinery breakdown.
  • Trained in a new facility for safety procedures and manufacturing process of asphalt roofing material.
  • Updated, monitored and enforced all safety procedures and regulations.
  • Demonstrated extensive knowledge of chemical and biological safety procedures.
  • Learned production and safety procedures required for Plant personnel.
  • Maximized equipment utilization while adhering to safety procedures.
  • Handled hazardous materials under the appropriate safety procedures.
  • Learned safety procedures within manufacturing environment.
  • Maintained quality and safety procedures.
  • Observe all safety procedures, including the use of appropriate safety devices and personal protective equipment (PPE)
  • Worked following 5S methodologies, ensuring that standards, requirements and safety procedures are followed.
  • Perform duties in compliance with Health & Safety procedures and Equipment Manuals.
  • Act within accordance of safety procedures in a production environment.
  • Comply with all Corporate and Commerce Safety procedures and policies.
  • Work with hazardous materials under the appropriate safety procedures.
  • Adhere to all safety procedures and practice good housekeeping.
  • Followed strict safety procedures while wearing required PPE.
  • Maintain proper safety procedures while performing job.
  • Adhere to all safety procedures and good housekeeping standards Support efforts to consistently exceed customer expectations.

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2. Batch Records

high Demand
Here's how Batch Records is used in Manufacturing Associate jobs:
  • Maintained batch records and logbooks to comply with regulatory requirements, manufacturing practices and aseptic processing of commercial products using Procedures.
  • Prepared production documents, including standard operating procedures, manufacturing batch records, inventory reports, and productivity reports.
  • Developed and reviewed manufacturing and automation process flow diagrams to create batch instructions for conversion into electronic batch records.
  • Executed manufacturing process steps using standard operating procedures associated with batch records and Solution Lot Records.
  • Perform material take outs and utilize electronic batch records on the manufacturing execution system.
  • Trained junior purification personnel on performing purification procedures and completing production batch records.
  • Assisted with writing/revising manufacturing instructions and batch records used for product production.
  • Operated manufacturing equipment in accordance with batch records and standard operating procedures.
  • Followed batch records and allocated necessary buffers and materials for purification processes.
  • Revised batch records and various production procedures for accuracy and precision.
  • Perform manufacturing Procedures using Standard Operating Procedures and Batch Records.
  • Authored standard operation procedures/batch records for various processes and equipment.
  • Reconcile and review finished manufacturing batch records upon completion.
  • Executed batch records and maintained documentation in equipment logbooks.
  • Reviewed batch records and determined acceptance/rejection of samples.
  • Completed batch records using mathematical calculations and formulas.
  • Review batch records/travelers, initiate/investigate problem reports.
  • Review batch records, and other applicable documentation to comply with regulatory requirements and good manufacturing practices (GMP's).
  • Assist in the review of documentation for assigned functions (equipment logs, routine area audits, batch records).
  • Assigned to review and ensure accuracy of Electronic Batch Records in alignment with PQA department prior to batch record closure.

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3. Cell Culture

high Demand
Here's how Cell Culture is used in Manufacturing Associate jobs:
  • Completed commercial biological production steps per regulations/procedures/schedule in manufacturing support, cell culture, and protein purification operations.
  • Performed fermentation, cell culture, and purification manufacturing operations to produce clinical and commercial biotechnology products.
  • Operate Cell Culture manufacturing equipment, instrumentation and daily activities in an organized and efficient manner.
  • Carried out critical cell culture and purification activities in aseptic manufacturing area with constantly evolving priorities.
  • Supported Cell Culture/Purification operations for the production of a bulk drug substance product.
  • Dispensed and formulated buffer solutions for Purification and Upstream Cell Culture.
  • Developed and implemented large scale manufacturing processes to optimize cell culture output
  • Perform cell culture manufacturing processes according to Standard Operating Procedures.
  • Performed cell culture and fermentation operations to synthesize media.
  • Supervised cell culture Technology Development lab and staff.
  • Certified trainer on purification and cell culture operations.
  • Received qualification on all Cell Culture equipment.
  • Performed aseptic manipulation of cell Culture.
  • Buffer and media preparation, both large and small scale, sterile and non-sterile to support cell culture and protein purification.
  • Trained new employees and conducted cross training on buffer and media processes to associates in cell culture and purification areas.
  • Tested for optimal protein production influenced by volumes of roller bottles and trained two associates how to perform cell culture.
  • Start up team member for Cell Culture Production Facility and Product Recovery Operations insuring GMP readiness meeting the project deadline.
  • Conducted cell culture assays to analyze cell growth to process only best lots improving yield by 10%.
  • Qualified trainer in all upstream operations (aseptic processing, large scale cell culture, media prep).
  • Reviewed cell culture and production manufacturing batch records for accuracy and completeness prior to submission for QA review.

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4. Cgmp Environment

high Demand
Here's how Cgmp Environment is used in Manufacturing Associate jobs:
  • Performed recovery and purification procedures for vaccines and other biological therapeutics at a manufacturing scale in a CGMP environment.
  • Followed all relevant standard operating procedures and complete master production records in a cGMP environment.
  • Performed cleaning and housekeeping activities for assigned areas as required maintaining a cGMP environment.
  • Completed work instructions and maintains cGMP environment to comply with regulatory requirements.
  • Manufacture RAD units (Renal Assist Devices) using cells cultured from human kidneys within a team-oriented class 10,000 cGMP environment.
  • Performed process activities associated with the production of drug substrate produced from mammalian cells in cGMP environment.
  • Followed standard operating procedures (SOP) per activity performed while working in a cGMP environment.
  • Perform all stages of the microbial fermentation process using a 2000L vessel within a cGMP environment.
  • Formulated various media and buffer solutions in a cGMP environment for Upstream and Downstream processes.
  • Worked in a cGMP environment performing assigned projects per written SOP's.
  • Perform and document daily operations in a cGMP environment.
  • Work is conducted in a clean room cGMP environment.
  • Experienced working in a cGMP environment and documentation.
  • Received and administered training in a cGMP environment.
  • Experience working in a cGMP environment.
  • Manufactured biologics in cGMP environment.
  • Performed large-scale protein purification according to SOPs in a cGMP environment.
  • Experienced in maintaining a cGMP environment and inspection ready workspace.
  • Implemented GRIPs ideas to improve the overall workflow while maintaining a cGMP environment.
  • Manufactured polyanhydride copolymers for Gliadel wafers in a cGMP environment.

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5. Assembly Line

high Demand
Here's how Assembly Line is used in Manufacturing Associate jobs:
  • Developed production plan for assembly line based upon availability of parts/boards and customer demand.
  • Completed daily tasks in production while operating assembly lines
  • General manufacturing of plastics food packaging assembly line
  • Participated in assembly line changeovers.
  • Assisted with the daily operations of the Parts Depot through shipping, receiving, assembly line packaging, and inventory management.
  • Cleaned 55 gallon plastic drums with a special chemical and the put them on assembly line then loaded them onto a truck
  • Worked in an assembly line for components, placement and assemble various types of receiver, amplifiers and other electronic components.
  • Certified and trained to operate four assembly lines which are used in the production of mid-range and heavy duty turbo chargers.
  • Wash valve bodies in an acid mixture to make sure they are clean and ready for assembly line in small parts.
  • Assemble various parts onto Nissan motors using air power tools, Inspect the motors as they move down the assembly line.
  • Fast paced assembly line work, understanding standardized work instructions, shipping, receiving items, some cell lead work.
  • Performed final assembly to a variety of products on an assembly line, inspected product and prepared product for shipment.
  • Worked in assembly line to built & assembled various types of electromotive auto parts for well known auto industries i.e.
  • Assembled supermarket scanners in an Assembly line environment with a focus on fast production and a high level of quality.
  • Operated automatic placement equipment to build high quantities of printed circuit assemblies on a fast paced assembly line.
  • Provided on the job training to 10-15 new employees on technical and procedural aspects of the assembly line.
  • Assemble Toyota car seats on an assembly line that is divided into 7 to 10 different work areas.
  • Controlled the number of blanket units manufactured on an assembly line by stopping and starting the machines.
  • Hand tools such as torques and ranches are also used on the assembly line in designated stations.
  • Manufactured the Honda Pilot and Honda MDX on Honda assembly line 2 in a fast pace environment.

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6. Clean Room Environment

high Demand
Here's how Clean Room Environment is used in Manufacturing Associate jobs:
  • Meet daily goals by interpreting and clarifying customers' specifications and complying with quality/safety standards within fast paced clean room environment.
  • Performed specific tasks in a controlled clean room environment utilizing good aseptic techniques and following company gowning requirements.
  • Perform testing on computerized equipment for the manufacturing of semiconductor devices within a clean room environment.
  • Maintain clean room environment and aseptic behavior to comply with regulatory requirements and good manufacturing practices.
  • Operated computerized water fabrication equipment for the manufacture of semiconductors in a clean room environment.
  • Operated silicon crystal saw and integrated circuit photo-lithography equipment in a clean room environment.
  • Performed housekeeping and sanitizing in a clean room environment.
  • Created them in a clean room environment also labeled, packaged, and quality checked every order before being sent out.
  • Performed testing, assembly, data collections and repair work in both dark room and clean room environments.
  • Trained and certified to operate all hand, power tools and machinery in a clean room environment.
  • Operated under an ISO class 6 and 7 clean room environment to ensure personal and product safety.
  • Worked under GMP regulations in a clean room environment for clinical and commercial cell culture products.
  • Assembled and processed silicon microchips for use in multiple electronic devices in a clean room environment.
  • Processed optical fiber in a clean room environment: safety glasses, gown and shoe covers.
  • Followed all quality and procedure protocol for behavior in a class 100 clean room environment
  • Operated lines of machinery that process computer chips in a clean room environment.
  • Work in a team oriented clean room environment to meet the needs of business
  • Preformed manual hand assembly of membrane electrode assemblies in a semi-clean room environment.
  • Assembled hard disk drives in a clean room environment.
  • Performed RF and particle testing in clean room environment.

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7. Cip/Sip

high Demand
Here's how Cip/Sip is used in Manufacturing Associate jobs:
  • Applied aseptic, CIP/SIP, dispensing, assembly of parts from blueprints, and equipment calibration practices.
  • Create Standard Operation Procedures for operation and care of autoclaves, parts washers and CIP/SIP skids.
  • Utilized DCS system for execution of CIP/SIP, transfers and buffer batching operations.
  • Performed Clean in Place / Steam in Place CIP/SIP for various equipment's.
  • Maintain, operate, and clean (CIP/SIP) all manufacturing vessels.
  • Contributed to start-up of facility after a 3-year shutdown by performing CIP/SIP.
  • Operate automated Buffer/Media/CIP/SIP process vessels through the use of HMI/SCADA systems.
  • Cleaned and sterilized equipment via CIP/SIP systems.
  • Performed CIP/SIP of product transfer lines.
  • Participate and support process improvement initiatives.Perform CIP/SIP/sanitization procedures.
  • Validated Process, Cleaning and Sanitization process (CIP/SIP) for Neulasta equipment.

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8. Raw Materials

high Demand
Here's how Raw Materials is used in Manufacturing Associate jobs:
  • Maintained Material Safety Data Sheets for incoming hazardous and non-hazardous raw materials.
  • Achieved work-in-process demands by allocating raw materials and manpower to avoid bottlenecks.
  • Maintained raw materials inventory for Purification and Solution prep areas.
  • Worked in a raw materials warehouse and manufacturing environment.
  • Documented and calculated information pertaining to obtaining raw materials.
  • Maintained inventory status of raw materials and consumables.
  • Determined production needs and procured raw materials.
  • Conducted analysis of raw materials.
  • Weigh or measure, label and assembly approved raw materials to be used in the manufacture of marketed or clinical products.
  • Prepared buffer and media solutions; weighed raw materials, mixing and transferring to bag or drum for future production use.
  • Utilize a computerized system(MES) to weigh and dispense raw materials for manufacturing operations and miscellaneous activities in MES.
  • Operate ovens; operate micrometer and other testing equipment; handle bare product; move raw materials and finished goods.
  • Facilitate the flow of raw materials between various production areas and controlled process of manufacturing for multiple lines of production.
  • Managed the supply chain for raw materials and finished product originating from and destined to sites around the world.
  • Verify the name and lot number of the product that the raw materials are to be used in.
  • Create toll cost batches produced by third-party vendors that utilize raw materials purchased and shipped to their facilities.
  • Weighed, measured and checked raw materials to ensure batches manufactured contained proper ingredients and quantities.
  • Maintain a constant visual on work being done and raw materials being used throughout the day.
  • Assist with finished material (cutting raw materials, or final material trim post-press procedures).
  • Enter and maintain operational data and pick raw materials, receive finished goods and scrap.

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9. Chromatography

high Demand
Here's how Chromatography is used in Manufacturing Associate jobs:
  • Performed therapeutic purification using affinity column chromatography.
  • Performed column chromatography and liquid extraction process as per the process requirements while maintaining safe manufacturing practices.
  • Performed protein purification using chromatography techniques; basic understanding of Unicorn based FPLC systems.
  • Developed an extensive knowledge of ultra-filtration, sterile filtration/transfer, and some column chromatography.
  • Performed protein purification utilizing column chromatography to create drug substance in mass quantities.
  • Performed protein purification process by using various column chromatography and UF/DF system.
  • Executed large-scale column chromatography, ultra-filtration and other purification and processing procedures.
  • Operate large-scale chromatography columns using RoseMount 3 and Delta V operating systems.
  • Purified therapeutic protein molecules using affinity, anion-exchange, and cation-exchange chromatography.
  • Performed large-scale protein purification using column chromatography and UF/DF filtration techniques.
  • Purified protein using various chromatography columns and virus removal filtration systems.
  • Operated Chromatography columns and ultra filtration skids to purify product.
  • Demonstrated proficiency with manual preparation and packing of chromatography columns.
  • Developed task specific training modules for column chromatography and homogenization.
  • Performed purification of protein using affinity and anion column chromatography.
  • Performed filtering and purification of our products using chromatography equipment.
  • Experience operating AKTA Pilot Chromatography skids using Unicorn software.
  • Prepared and operated chromatography machinery for protein purification process.
  • Operated and monitoring downstream process including chromatography process operation.
  • Prepared various buffers for packing and testing chromatography columns.

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10. FDA

high Demand
Here's how FDA is used in Manufacturing Associate jobs:
  • Used to manufacture intermediates and/or final bulk product of acceptable quality to meet FDA and/or European Regulatory quality requirements.
  • Conducted aseptic manufacturing operations adhering to FDA national guidelines and internal operating procedures.
  • Recognized for exemplary contribution in preparation for FDA PAI inspection.
  • Perform manufacturing, validation, and commissioning operations (IQ; OQ; PQ and PV), according to GMP/FDA.
  • Utilized 5S, LEAN and GMP principles to produce quality products that meet Food and Drug Administration (FDA) guidelines.
  • Required precision, thorough documentation, and adherence to strict operating procedures set forth by the company and the FDA.
  • Reviewed manufacturing documents for completeness, accuracy and compliance with GLP and FDA Quality System Regulations (QSR).
  • Performed audits on training records to ensure all team member were in compliance according to FDA and GMP guidelines.
  • Documented and applied knowledge of autoclave use, FDA Regulations, and knowledge of SOP's and CGMP's.
  • Served in leadership role in California FDA audit of new facility that was subsequently granted a manufacturing license.
  • Perform all duties in accordance with GMP under FDA, MHRA and European Union policy and established procedures.
  • Assist in the skilled manufacturing of pharmaceutical products, complying with all FDA regulations and quality assurance standards.
  • Manufactured clinical-grade stem cell therapy drug products to be used in all phases of FDA approved clinical trials.
  • Assisted with FDA validating processes and equipment that are directly related to filtration, cleaning and sterilization.
  • Complete audits and prepare production areas for FDA, EU, EMEA, and Japanese regulatory inspections.
  • Lead the Cell Culture team from Start-Up to Phase Three Clinical to FDA Approval under Baxter.
  • Have prepared for and been present for numerous FDA, Canadian, Japanese and European inspections.
  • Trained in the Lathing and Milling operations Review and process all associated production records per FDA regulations
  • Collaborated with management to write and review FDA compliant work instructions and standard operating procedures.
  • Represent manufacturing as the SME for internal audits, partner audits, and FDA audits.

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11. Aseptic Technique

high Demand
Here's how Aseptic Technique is used in Manufacturing Associate jobs:
  • Train personnel in Fill and Finish and Bulk Plants in environmental monitoring, aseptic techniques and environmental monitoring equipment.
  • Operated and maintained equipment using aseptic technique causing me to become proficient in manufacturing operations.
  • Experienced with aseptic technique including in-process and final product sampling and delivery utilizing LIMS system.
  • Served as Qualified Trainer for manufacturing training programs including aseptic techniques and equipment qualification.
  • Ensured adherence to Good Manufacturing Practices, standard operating procedures and aseptic technique.
  • Trained coworkers in aseptic techniques and processing and performed filtration/column packing.
  • Collected in-process samples of product using aseptic technique during filling operations.
  • Perform sampling using aseptic technique, manufactured media and buffer solutions.
  • Performed sampling using aseptic techniques and recorded critical process parameters.
  • Used aseptic technique to ensure prevention of product contamination.
  • Acquired experience with aseptic techniques and general laboratory practices.
  • Facilitated in training of technician aseptic techniques.
  • Performed aseptic techniques during product transfer.
  • Use of aseptic techniques to perform inside the clean room, class 100,000 and 10,000 including the Biological safety cabinets.
  • Use of aseptic technique within biological safety cabinet for sample processing, cell culture inoculation, and supplement preparation.
  • Demonstrate good knowledge of aseptic techniques in cell splits, thaws, and environmental monitoring.
  • Used all clean room and aseptic techniques during processes and functions ongoing at EPA sites.
  • Clean room and aseptic techniques, microbial testing and detection on products or contact surfaces.
  • Certified in Aseptic techniques, environmental monitoring (gowning and EM samples).
  • Practiced aseptic technique while executing process sampling of product using laminar flow hood.

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12. Quality Checks

high Demand
Here's how Quality Checks is used in Manufacturing Associate jobs:
  • Performed quality checks and calculations to ensure adherence to all manufacturing and regulatory protocol.
  • Performed quality checks as required to ensure product met specifications.
  • Perform quality checks utilizing buddy system method of quality assurance.
  • Performed quality checks on microchips utilizing automated microscopes.
  • Complete required quality checks and documentation.
  • Preformed quality checks, 5 s, and would keep track of efficiency and downtown via paperwork every 2 hours.
  • Spearheaded adoption and implementation of quality checks, which resulted in a defect free reduction rate of 99%.
  • Deliver finished material, maintain clean and safe work area, perform periodic quality checks, repair minor defects.
  • Perform secondary operations, clean and count finished parts, and assist with quality checks and procedure audits.
  • Coordinated periodic bin audits, and quality checks to ensure accurate inventory for the product lines.
  • Worked in the smart handle department, building and performing quality checks on door handles.
  • Maintain quality checks every 15 minutes, and ensure specifications are within engineering standards.
  • Performed ESPC checks, quality checks and maintained product flow for the entire line.
  • Perform various quality checks, cleaning, and change-over of machine equipment.
  • Conducted pressure tests and quality checks on all parts for quality assurance.
  • Inspected work in progress and final quality checks prior to packaging.
  • Performed quality checks on products and parts while working independently.
  • Perform quality checks on jets and airplane part called TO5.
  • Perform quality checks on terminal seating and placement.
  • Perform quality checks on labels and codes.

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13. Troubleshoot

high Demand
Here's how Troubleshoot is used in Manufacturing Associate jobs:
  • Provide Manufacturing input for troubleshooting, deviation analysis and problem solving activities related to the manufacture of intermediates and Drug Substance.
  • Provided guidance to technician to troubleshoot issue related to solid oral dosage form tablet in particular at production facility.
  • Shift Lead responsible for planning and execution of daily production activities, troubleshooting equipment problems and general issue resolution.
  • Supported Manufacturing set-up, operation, troubleshooting and dismantling of equipment used for the preparation of drug delivery systems.
  • Support clinical manufacturing activities in the Manufacturing Plant, including equipment set-up, operation, troubleshooting, and dismantling.
  • Maintain high level of mechanical and technical aptitude; actively participating in effective troubleshooting of equipment and processing problems.
  • Complete all associated required documentation, while working with company engineers on tool troubleshooting and process improvement.
  • Utilize mechanical knowledge to successfully complete equipment changeovers and conduct troubleshooting of equipment through root cause analysis.
  • Assist the protein purification manufacturing group with troubleshooting of process equipment and technical advice on processing issues.
  • Assisted in troubleshooting technical issues and problems, identified deviations and collaboratively participated in the investigations.
  • Involved in troubleshooting and research projects aimed at improving overall efficacy and potency of medication.
  • Participated in mentoring and training other associates on troubleshooting and processes on the manufacturing floor.
  • Implemented troubleshooting documentation for repair so that downtime on hardware failure is minimized during manufacturing.
  • Operate and troubleshoot manufacturing equipment and work closely with management and Quality as necessary.
  • Collaborate with department in cross-functional teams, projects and GMP-related problem resolution and troubleshooting.
  • Operate, maintain and troubleshoot manufacturing and testing equipment, ensuring uninterrupted production.
  • Demonstrated ability to organize and troubleshoot in a fast-paced environment without sacrificing quality.
  • Provided troubleshooting support to manufacturing operations and participated in cost efficiency improvement efforts.
  • Performed operational qualifications, performance qualifications as well as equipment troubleshooting.
  • Monitored equipment, performed maintenance and troubleshooting equipment to reduce downtime.

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14. Quality Standards

high Demand
Here's how Quality Standards is used in Manufacturing Associate jobs:
  • Interpreted schematic drawings, blueprints, and manufacturing assembly processes to ensure quality standards and customer satisfaction.
  • Produced parts in accordance with company quality standards on manufacturing line.
  • Meet rigid vendor quality standards by evaluating integrity of materials.
  • Adhered to quality standards and regulatory compliance.
  • Assisted with ensuring handcuffs meet quality standards
  • Achieved quality standards by quickly and accurately assembling, testing, marking and packaging products for on-time delivery to global customers.
  • Achieve aggressive daily work in process goals by interpreting customers' specifications, complying with quality standards and implementing technical processes.
  • Utilized time efficiently and proactively to track, expedite, and prioritize product to meet quality standards and on time delivery.
  • Make work station adjustments, tool and fixture changes as required to maintain quality standards and facilitate changeovers of product types.
  • Perform production and quality standards related to customer returns by verifying that the information related to the receiver is correct.
  • Meet daily goals including quality standards and customers' specifications by implementing diffusion processes within Class 100 Clean Room.
  • Received Above Average job performance reviews for productivity, excellent learning skills and compliance with quality standards.
  • Maintained specification charts, tool changes, and other miscellaneous records required to maintain quality standards.
  • Repaired aluminum and steel body parts to meet quality standards and packaged finished product.
  • Recognized for meeting quality standards by applying skill and thorough knowledge of multiple processes.
  • Operated Wave Solder ensuring all soldered assemblies complied with quality standards.
  • Performed in-process testing and adjustments to ensure product meets quality standards.
  • Check to make sure every part meets up to quality standards.
  • Assembled chest drains from start to finish with high quality standards.
  • Measured parts to ensure that they met or exceeded quality standards.

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15. ISO

average Demand
Here's how ISO is used in Manufacturing Associate jobs:
  • Advised immediate supervisor of need for additional machine repairs and recommend equipment modifications to achieve improved operation.
  • Consulted with designated individual or immediate supervisor on any electrical malfunction or repairs for course of action.
  • Administer the daily manufacturing functions related to mammalian cell culture to isolate and obtain therapeutic protein products.
  • Utilized different agar and technique for each environmental area for identification and isolation the pathogenic microorganism.
  • Intern Assisted in a variety of manufacturing positions while observing supervisory techniques and labor deployment strategies.
  • Earned positive reputation with supervisor by exceeding customer ship quotas and preparing accurate reports.
  • Maintained documentation to insure yearly compliance with ISO standards using Master Control application.
  • Assured exceptional customer satisfaction and the highest quality by complying with ISO9000 specifications.
  • Collaborated with managers, supervisor and QA/QC for operational management and process improvement.
  • Initiate deviation investigations and implements corrective and preventative actions as required by supervisor.
  • Worked with sanitation supervisor to troubleshoot and problem solve to eliminate product contamination.
  • Assist engineering and manufacturing supervisors in tasks related to production.
  • Followed strict ISO-compliant manufacturing procedures and all policies and procedures.
  • Conferred with supervisor to receive instructions and exchange production information.
  • Performed additional duties as assigned by supervisor and/or lead associate.
  • Completed all aspects of medical device assembly using ISO requirements
  • Performed process related environmental monitoring in ISO100/Grade 5 area.
  • Trained other operators, assisted other operators and supervisors.
  • Work with Warehouse Supervisor in product organization and storage.
  • Provided supervisory backup in Supervisor's absence.

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16. Bioreactors

average Demand
Here's how Bioreactors is used in Manufacturing Associate jobs:
  • Qualified trainer for Tissue Culture, Wave-Bioreactors, Clarification, and ELISA assays.
  • Participated in an investigation regarding interferon variability's by operating bench top bioreactors and analyzing data.
  • Performed expansion, inoculation and continuous monitoring of bioreactors as per the process requirements.
  • Performed manufacturing unit operations utilizing bioreactors, centrifuges, and depth/sterile filters.
  • Upstream-operated purification skids and bioreactors.
  • Experienced with small and large scale bioreactors, tangential flow filtration (TFF) skids, and cell harvest clarification trains.
  • Participated in validation of cleaning systems Clean-In-Place and Steam-In-Place for small scale vessels and bioreactors using Delta V automation.
  • Performed 10L to 2000L bioreactors various harvesting and purification operations during a process as per the client requirements.
  • Participate in equipment set to work and return to service activities in Bioreactors and Media Preparation areas.
  • Operated equipment such as tanks, filtration systems, carton assembler, bioreactors, and production lines.
  • Prepared, set up, operated and maintained Small Scale Bioreactors to grow mammalian cells.
  • Handled validation of bioreactors, deviations investigation, tech transfers, and process development.
  • Operated bioreactors, tanks, agitators, filtration devices, centrifuges, and computers.
  • Promote scaling-up cellular processes from spinner-flasks to large volume stainless steel/ single-use bioreactors.
  • Qualified to run skids, bioreactors, and harvest vessels in Upstream suites.
  • Perform PM and assist in validation/qualification of bioreactors, NOVA and SCADA system.
  • Performed monthly PM of Upstream equipment (Bioreactors, Incubators, etc.)
  • Acted as contact for PM of all bioreactors by the maintenance department.
  • Operated 100L, 750L, and 2000L bioreactors using delta V system.
  • Operated, sterilized, and sanitized bioreactors, lines, and vessels.

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17. Conductivity Meters

average Demand
Here's how Conductivity Meters is used in Manufacturing Associate jobs:
  • Perform calibration/verification of scales and test instruments; efficient in PH/Conductivity meters.
  • Operated other related equipment such as glass-washer, autoclave, filter integrity tester, pH and Conductivity meters.
  • Operate autoclave, filter integrity testers, temperature probes, pH/conductivity meters and CIP/SIP skids.
  • Standardized scales and calibrated pH and conductivity meters prior to processing.
  • Operated laboratory equipment including pH and conductivity meters, spectrophotometers, microscopes and incubators.
  • Operate analytic instruments include pH and conductivity meters, balances and spectrophotometers.
  • Participated in operation of pH meters, conductivity meters and osmometers.
  • Calibrated and used conductivity meters and ph meters and temperature devices.
  • Provide support for various engineering protocols * Operate analytic instruments include pH and conductivity meters, balances and spectrophotometers.
  • Follow procedures to operate pH meters, osmometers, spectrophotometers and conductivity meters.
  • Performed Standardization of Analytical and Table Top Balances and PH Conductivity Meters, Hamo and Lancer washers.

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18. Production Equipment

average Demand
Here's how Production Equipment is used in Manufacturing Associate jobs:
  • Followed accurate verbal and written procedures in operating production equipment and performing processing steps; accurately completing appropriate production documentation.
  • Operated manufacturing production equipment, under as required by Master Manufacturing Records and Standard Operating Procedures.
  • Operated general production equipment such as Autoclaves, Incubators, and pH/Conductivity meters.
  • Executed all material transportation of all production equipment and finished pharmaceuticals products.
  • Maintained high level of housekeeping of production equipment and associated areas.
  • Coordinated with engineering department and technicians to resolve production equipment issues.
  • Supported production equipment set-up and maintenance.
  • Operated and/or monitor production equipment.
  • Possess strong technical, mechanical and troubleshooting skills in all production equipment and manufacturing processes for solids and liquids dosage forms.
  • Operated production equipment such as autoclave, centrifuge, incubator and pH conductivity meter and trained other associates as required.
  • Operate general production equipment (such as pH and conductivity meters, autoclave, portable mixers, etc.).
  • Operated, disassembled, cleaned, sanitized, sterilized, reassembled and maintained all production equipment in good working order.
  • Cleaned production equipment in accordance with clean room standards, including TOC swabbing for residual compounds.
  • Operated various pieces of equipment throughout the facility, assisted with sanitation and maintaining of production equipment.
  • Perform assembly, cleaning, sanitizing, and steaming of production equipment for the Manufacturing Process.
  • Prepare, process, and sterilize production equipment, report and document variances from specs.
  • Operated production equipment in accordance with SOP's, involving the use Cellmate Robotic systems.
  • Operated production equipment, verified weights and measurements, inspected and prepared raw materials.
  • Clean, sterilize, and disinfect production equipment and rooms in a complaint manner.
  • Performed SIP/CIP on production equipment, as well as transferring of harvested material.

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19. Protein

average Demand
Here's how Protein is used in Manufacturing Associate jobs:
  • Developed purification processes used for the clinical and commercial manufacture of therapeutic proteins group by running bench and pilot-scale purification experiments.
  • Performed protein syntheses (insulin and carbohydrate complex) in a fast-paced environment by following and developing written protocols.
  • Performed adjustments based on data analysis; also conducted separation and protein filtration of product.
  • Perform operations of laboratory equipment and laboratory methods such as protein purification, conjugation
  • Trained other Manufacturing Associates on cleaning validation protocol used in protein production.
  • Perform protein purification for rare genetic diseases in a manufacturing environment.
  • Handled manufacturing of therapeutic proteins under GMP conditions.
  • Performed large-scale purification of several protein drugs.
  • Determined protein concentrations using A280.
  • Prepare buffer/media for protein addition.
  • Worked in a team setting performing in the downstream protein purification process for the development of intravenous pharmaceutical products.
  • Operate FPLC to purifying protein through Affinity, Ion Exchange, and Size Exclusion column in clean room.
  • Sample testing: pH, Conductivity, Turbidity and Protein concentration (Solo VPE) 2.
  • Acquired familiarity with the operation of AKTA protein purification systems and HPLC use in manufacturing.
  • Execute basic analysis of process samples such as pH, conductivity, and protein concentration.
  • Utilized Standard Operating Procedure's and Batch Record instruction to purify Plasma proteins.
  • Involved with the extraction of cells through columns for protein mass collection.
  • Lead tech transfer and processing of protein recovery and large scale purification.
  • Lead the Protein Purification Department in the Production of StreptAvax and FIV.1.
  • Performed downstream processes such as protein purification and ultra - filtration.

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20. Process Equipment

average Demand
Here's how Process Equipment is used in Manufacturing Associate jobs:
  • Operated process equipment associated with all phases of protein production and purification, including monitoring and controlling process variables.
  • Maintained operational safety condition of production areas and process equipment that minimized safety hazards in the work area.
  • Ensured process equipment is appropriately maintained for operation and conducted daily activities in an organized efficient manner.
  • Ensured that all membrane process equipment was properly setup and operated to all engineering specifications.
  • Monitored process equipment and building management system, and reported out status per approved procedures.
  • Trained personnel on methodology of business operating software and how it interfaces with process equipment.
  • Operated, maintained and troubleshot pharmaceutical process equipment during manufacturing process.
  • Cleaned process equipment and checked conductivity levels under GMP guidelines.
  • Operated glass and carboy washers, autoclave/sterilization process equipment.
  • Used Omega Data logger for the temperature mapping during the validation on Sterilization-In-Place of process equipment and pipelines.
  • Operated cleaning process equipment, such as COP bath, glass washer, and carboy washer.
  • Work with process equipment controlled by a Terminator PLC and C-More HMI.
  • Assembled numerous types of process equipment; provided maintenance and trouble shooting.
  • Maintain and calibrated process equipment, hot plates and ovens.
  • Operated SPEEDFAM and IPEC chemical mechanical polishing process equipment.
  • Cleaned and assembled process equipment.
  • SIP and CIP process equipment.
  • Supported process equipment cleaning/sterilization/sanitization validation.
  • Coordinated with facilities and engineering support groups to ensure proper maintenance of bioprocess equipment.
  • Supported cleaning and sterilization validation, CIP, COP, SIP, and autoclave process equipment using Kaye/GE Validator 2000.

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21. Hand Tools

average Demand
Here's how Hand Tools is used in Manufacturing Associate jobs:
  • Operated multiple hand tools and assigned production or manufacturing machinery in a manner that supports quality assurance.
  • Work with hand tools and drivers for proper installation of memory (RAM), processors and other components.
  • Use of fork truck and various hand tools; mechanical / visual inspection / troubleshooting / repair of equipment.
  • Experience in machine shop working with various hand tools, power tools, repairing and fabricating various equipment.
  • Wired components, hand soldered, disassembled, modified, and reworked units using various hand tools.
  • Perform routine and repetitive operations using small power/pneumatic tools, hand tools, and/or other machinery.
  • Operated various CNC machines, used various hand tools to perform tool changes and change overs.
  • Interpreted process details, drawings and sketches then assembled computers with pneumatic and hand tools.
  • Utilized hand tools to assemble cabs, following schematics to ensure the correct operation.
  • Manufacture furniture using hand tools, Adhesives, jigs, fabrics and other component.
  • Operate power equipment to move merchandise; utilizes small hand tools & pallet handlers.
  • Use hand tools and power tools to assemble units according to product specifications.
  • Finished edges of metal components using various types of hand tools and machinery.
  • Used a variety of hand tools to complete the task at hand.
  • Use of hand tools and power tools to assemble parts to vehicles.
  • Follow blueprints; Assemble parts to units using hand tools and screws.
  • Set up and uses basic hand tools and machines as needed.
  • Operated various presses and hand tools to complete daily quota.
  • Assist in calibration hand tools used in the manufacturing processes.
  • Operated Stud Guns, Hydraulic Punches and numerous hand tools.

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22. Production Process

average Demand
Here's how Production Process is used in Manufacturing Associate jobs:
  • Manage production processes for GMP manufacturing operations including initiating new systems, process improvements equipment, and procedures.
  • Streamlined production processes and implemented cost-reducing measures aimed at addressing critical production inefficiencies and logistical gaps.
  • Monitor manufacturing process quality to assure that only acceptable materials are released to subsequent production processes.
  • Analyze and refine production processes; primarily to increase efficiency and labor flexibility.
  • Experience in the manufacturing production process, warehouse/distribution, quality inspection and packaging.
  • Apply lean concepts to improve production processes and manufacturing efficiency.
  • Performed production process database system queries and trend analysis.
  • Assisted company with improving production processes and safety.
  • Validated cell culturing and media production processes.
  • Conducted technical audits hourly on production process.
  • Operated machinery used in production process.
  • Correspond with other departments, such as maintenance and test technicians, to analyze and solve disturbances within the production process.
  • Received training and gained much experience with computer applications relating to the production processes, and in other general computer applications.
  • Entered recorded changes in batch data in records and distributed the records to the next step in production process.
  • Managed to gather, record, analyze and communicate charts from the production process to present to management.
  • Increased efficiency up to 50% by developing manufacturing fixtures and aids for use in production processes.
  • Trained new employees in production processes and performed lead responsibilities in the absence of senior associates.
  • Make sure that appropriate safety measures are considered at every step of the production process.
  • Optimized the production process and improved quality for the development of an artificial liver device.
  • Streamlined and organized a filing system to improve the paper work production process in IFS.

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23. Ensure Compliance

average Demand
Here's how Ensure Compliance is used in Manufacturing Associate jobs:
  • Conducted internal audits for Quality Management System Procedures at multiple sites to ensure compliance and standardization of processes across all facilities.
  • Validated the integrity of products by analyzing and monitoring work processes to ensure compliance with quality standards and specifications.
  • Perform manufacturing auditing process in quality and safety to ensure compliance with all applicable regulations and policies.
  • Eliminated errors by closely monitoring work-in-progress to ensure compliance with quality inspections.
  • Maintain a quality presence to ensure compliance with all regulatory requirements.
  • Performed quality assurance inspection to ensure compliance to manufacturing specifications
  • Monitor department schedules to ensure compliance of established expectations.
  • Monitored operations to ensure compliance with process specifications.
  • Analyze and test complex radio and satellite receiver units, power amplifier, and control exciter to ensure compliance with specifications.
  • Performed internal audits (Process, Documentation & EHS) to ensure compliance with manufacturing processes.
  • Inspected parts and tooling per blueprints to ensure compliance with the Federal Aviation Administration.
  • Monitor and audit work processes to ensure compliance and completion of targets.
  • Interact with QC to ensure compliance with USP and Standard Operating Procedures.
  • Used Statistical Process Controls to ensure compliance with customers' specifications.
  • Assist engineering develop new business product process.Monitor department schedules to ensure compliance of established expectations.
  • Participated in self-audits to ensure compliance with safety and GMP requirements, and performed secondary review of MPDs.
  • Maintain and prepare high quality documentation.- Maintain at least an 95% cGMP training proficiency to ensure compliance
  • Lead pre-audit walkthroughs to ensure compliance with cGMP standards.

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24. Validation Protocols

average Demand
Here's how Validation Protocols is used in Manufacturing Associate jobs:
  • Prepare and run TSB media fills and filtration processes for execution of aseptic filling/filtration validation protocols.
  • Author and review validation protocols, standard operating procedures, and final reports for development qualifications.
  • Monitored critical manufacturing processes and executed routine validation protocols inside a Class 100 aseptic room.
  • Reviewed and evaluated methods development and validation protocols and reports to support the manufacturing process.
  • Operated manufacturing equipment, instruments and Executed equipment qualification protocols and validation protocols.
  • Performed process and equipment qualification and validation protocols; perform comparability studies.
  • Perform Validation Protocols for specific projects in compliance with industry guidelines.
  • Authored validation protocols and reports of major equipment and manufacturing process.
  • Participated in new facility start-up; executed commissioning and validation protocols.
  • Supported engineers in executing validation/re-validation protocols on process equipment and systems.
  • Initiated validation protocols and testing for various processing equipment.
  • Execute routine validation protocols and initiate quality incidents.
  • Execute validation protocols on small scale fermentation equipment.
  • Performed validation protocols of equipment and manufacturing process.
  • Perform validation protocols and initiate quality incidents.
  • Execute equipment qualification protocols and validation protocols.
  • Supported the execution of routine validation protocols.
  • Assisted with execution of validation protocols.
  • Performed Validation protocols for validating equipment.
  • Review and execute validation protocols.

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25. Lims

average Demand
Here's how Lims is used in Manufacturing Associate jobs:
  • Participated in environmental Health & Safety activities and maintained LIMS system for quality.
  • Trained in LIMS program to be responsible of samples collection, work list generation and submission of samples.
  • Implemented cost saving strategies and reduced wasteful spending on raw materials by 30% utilizing SAP & LIMS.
  • Experienced in using Atlas, LIMS, and PI Data Historian program to assist in floor operations.
  • Sample submission for Raw Materials testing through Sapphire software (LIMS) on a constant basis.
  • Verify SM LIMS templates for sampling, generated documentation and sample results for validation report.
  • Interfaced with Distributed Control Systems and other automated systems including POMS, LIMS/NGL, IMPACT.
  • Work with material reconciliation, EBR, WERUM system, LIMS and manufacturing processes.
  • Trained to proficiently operate SAP, GLIMS and DeltaV Manufacturing Associate: Media Prep/15K.
  • Use of Electronic Batch Record (EBR) and LIMS system for Samples collection.
  • Worked with ETTS, QUMAS, and QLIMS data systems to ensure regulatory compliance.
  • Set up lab computer and taught staff members how to operate LimsLink.
  • Perform samples chain of custody and results recording using LIMS system.
  • Used Oracle and LIMS for entering data and closing out orders.
  • Perform chain of custody for samples of filling process with LIMS.
  • Register samples in LIMS system and initiate chain of custody.
  • Perform viable monitoring and log samples into the LIMS system.
  • Managed LIMS system to provide QC Microbiology method integration.
  • Trained to proficiently operate SAP, GLIMS and DeltaV.
  • Requested sample retains using LIMS systems.

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26. Set-Up

average Demand
Here's how Set-Up is used in Manufacturing Associate jobs:
  • Initiated process set-ups, intermediaries, and dismantling and sterilization equipment after process was completed.
  • Determine production line set-up procedures and tooling for soldering according to specifications.
  • Operated, set-up and monitored automatic equipment for semiconductor products.
  • Place product in designated packaging receptacles following standardized set-up.
  • Assisted senior operators with set-up and tooling changeovers
  • Worked in Formulation Process: hands-on operations, set-up, clean, sanitize and prepare media and buffers per procedures.
  • Helped with machine set-up and tear down by prepping new paper rolls using manual crane lift and utility knife.
  • Review set-up sheets and specification to determine set-up procedures, machining sequences and dimensions of finished work pieces.
  • Assisted and was responsible in the set-up packaging area for communicating with various vendors and departments.
  • Performed all areas and duties of Machine such as set-up, operating, & packing procedures.
  • Make the required number of set-ups needed for each line(10 lines).
  • Assisted other operators with machine set-up and helped with the operation as needed.
  • Performed equipment CIP, SIP, set-up, and preparation for manufacturing use.
  • Clean, set-up, maintain and document equipment preparation for commercial production.
  • Closed out orders, gathered materials, required paperwork for next set-up.
  • Performed machine set-ups, tool changes as necessary and routine machine checks.
  • Pulled and set-up parts for cabinet assembly according to move ticket instructions.
  • Provided support during the equipment set-up, assembly, and cleaning activities.
  • Build bio- assembly and filter set-ups.
  • Identify proper tools for machine set-ups.

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27. Data Entry

average Demand
Here's how Data Entry is used in Manufacturing Associate jobs:
  • Inspected medical parts using a microscope for 12 hours* Worked with confidential material* Conducted data entry regarding results of inspection
  • Maintained inventory control by performing data entry before and after each chemical usage.
  • Performed computer-related clerical duties, including data entry and preparation of statistical reports.
  • Performed data entry and scientific calculations.
  • Well versed in spread sheet and other data entry programs for tracking of product through wafer fabrication processes.
  • Completed reports, required documentation, and performed data entry to ensure accuracy of processes.
  • Performed supporting activities including process set up, computer data entry and batch record review.
  • Construct VBA Excel data entry and matrix tracking spreadsheet for BOP program.
  • Worked on data entry for start up of a new business system.
  • Well versed in numerous data entry programs for organization of processes.
  • Help production line with sub-assembly, data entry for Non-conforming Materials.
  • Operate PC based computer terminals for data entry and retrieval.
  • Manufactured Computer Parts, Data Entry, Filled Orders for clients
  • Performed general office tasks including data entry and filing.
  • Performed data entry and processed work orders.
  • Performed daily data entry and filing.
  • Performed data entry on custom software.
  • Created Training Documents for test machine operation and maintenance Trained new employees on test machine operation and engineering data entry
  • EXPERIENCE: Water spider Right hand stuffer Right hand prep/Left hand prep Data Entry Function testing and Full Function testing Tacoma gun
  • Assisted MSAT in alleviating backlog of downstrean data entry for processes executed in the Portsmouth site.

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28. Circuit Boards

average Demand
Here's how Circuit Boards is used in Manufacturing Associate jobs:
  • Operated computerized equipment to pinpoint defects on printed circuit boards and removed excess material to ensure proper functioning.
  • Manufacture printed wiring circuit boards from bare board status to an electronically populated assembly.
  • Implemented upgrades on printed circuit boards according to work instructions/engineering drawings.
  • Populated circuit boards using customer specification work orders.
  • Worked as a repair specialist for BGA, Gate Array, Open Traces and lifted pads on printed circuit boards.
  • Inspected printed circuit boards(PCB's)for visible defects and replaced all damaged components by rework and repair.
  • Tested and programmed circuit boards Group leader for test department Trained new production workers Assigned daily assignments to the test department
  • Performed a variety of manual and/or automated tasks to assemble, test, repair, and pack completed circuit boards.
  • Inspected Printed Circuit Boards (PCB) for visible defects and replaced all damaged components by network or repair.
  • Work in R&D with Engineering on prototypes using schematics to make modifications on prototype circuit boards.
  • Assembled, reworked, tester, inspected, and troubleshoot electronic circuit boards and wired test boxes.
  • Build circuit boards following a blue print, Build chassis reading a schematic, Performing internal wiring.
  • Improved assembly process, which identified correct components and verified surface mount placement on circuit boards.
  • Conducted final test verification for accuracy of built circuit boards before sending to finished goods.
  • Operated a variety of production lines in the assembly of electronic circuit boards and components.
  • Inspected printed circuit boards for compliance to company guidelines, using test equipment.
  • Involved in the testing of experimental, pilot, or prototype circuit boards.
  • Change the line over frequently to accommodate the different circuit boards we manufacture.
  • Used insertion equipment both radial and axial to populate printed circuit boards.
  • Interpreted bill of material schematic drawings and soldered components onto circuit boards.

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29. Final Inspection

average Demand
Here's how Final Inspection is used in Manufacturing Associate jobs:
  • Experience with final inspection, final packaging, and semi-operated machinery.
  • Performed final inspection of finished product and reports final inspection reports.
  • Performed final inspections on medical device units per quality requirements.
  • Conduct incoming in-process and final inspections.
  • Finished off the cooked tools by fixing blemishes and then ready for final inspection before final cooking.
  • Conducted final inspections of packed optic fibers, insuring a quality product free of defects.
  • Conducted final inspection on wafers to detect defects using high and low power microscopes.
  • Performed the final inspection to ensure the quality of the finished product.
  • Performed final inspection for any malfunctions or defects and performed repairs.
  • Packaged product which has passed final inspection for final packaging.
  • Assembled, tested and performed final inspection of the computers.
  • Do a final inspection of the headlights for overall quality.
  • Performed final inspection on product.
  • performed visual in-process and final inspections and tests verifying quality conformance.
  • set up reels and boards for automated system, inspected assemblies from solder paste to oven, and final inspection.
  • Performed final inspection and grade each microarray for customer use.
  • Perform final inspection of intraocular lenses.
  • Performed the visual, weight, spray, manicure and final inspection process for Cypher Stent.

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30. CNC

low Demand
Here's how CNC is used in Manufacturing Associate jobs:
  • Operated CNC cutting system, knitted finished materials, completed quality inspections
  • Perform production assembly operations on CNC-Machining.
  • Machine operator - Ran CNC machines to cut raw castings into parts ready for assembly.
  • Finish all CNC machined parts to meet each customer's final specifications.
  • Operated CNC lathes, mills, and induction heat treats.
  • Experienced with the various types of CNC and PLC machines.
  • Operate CNC machines to construct needles for EV1 fuel injectors.
  • Assisted CNC Machine Operators to successfully operate CNC machines.
  • Set up a CNC machine to cut molded parts.
  • Utilized CNC machinery to cut glass for samples.
  • Operated CNC lathes and milling machines.
  • Operate manufacturing equipment in a high volume production environment using cnc machines and assembly equipment.
  • Assemble brake calipers Machine caliper housings Inspect components for acceptable quality Tool set on Chiron CNC machines Operate, calibrate C.M.M.
  • Job duties included re welding, rework operating cnc machines, machine cleaning, inspecting parts.
  • Implemented and maintained 5S inside CNC workcell.
  • Programmed and operated CNC drill machine Completed PC Boards Inspected completed boards, corrected defects
  • Programmed and operated CNC machines Completed PC boards Achieved all designated tasks
  • Operate, adjust, maintain (3) Fadal CNC Vertical Mills .

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31. Capa

low Demand
Here's how Capa is used in Manufacturing Associate jobs:
  • Achieved maximum operating capacity of production lines using Oracle database to manage and assign materials.
  • Resolved problems using root cause analysis to eliminate issues and restore operation to maximum capacity.
  • Performed Production Supervisor duties for a period of four months while Production Supervisor was incapacitated.
  • Performed process/equipment cleaning validation activities, non-conformance investigations, CAPA, and FMEA assessments.
  • Participated in company organized CAPA training and manufacturing department internal audits.
  • Monitor and report on Capacity and Material requirements for Production.
  • Operated and maintained single/multiple CNC machines with various capabilities.
  • Supported effective and timely deviation investigations and CAPA completion.
  • Give support to CAPA(corrective actions/preventive actions) on research related to an incident in the area of manufacturing.
  • Provided support to NC CAPA team for the root cause analysis when related to component prep area process issues.
  • Worked with QA department to close deviations (CAPA) and create SOP's for use in manufacturing.
  • Improved yield by completing preventive maintenance on grinders to maximize operating capacity of equipment and work in process.
  • Assisted in and documented investigations of deviation events in support of developing Root Causes and CAPA's.
  • Applied knowledge of processes, equipment and system capability to set challenging individual and facility standards.
  • Participate in revision and implementation if CAPA's in SOP's, forms and documents.
  • Interacted with others in a leadership capacity in order to ensure the meeting of quotas.
  • Worked with CAPA team for solving the manufacturing errors and problems pertaining to the processes.
  • Maintained high energy level, capable of working overtime as required to meet customer needs.
  • Performed investigations into lot failures by following CAPA, NCMR, and Variance procedures.
  • Designed the department's NC/CAPA program including formal report writing and quality data trending.

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32. Preventative Maintenance

low Demand
Here's how Preventative Maintenance is used in Manufacturing Associate jobs:
  • Prepared media and reagent preparation duties; performed inventory and stocking duties and equipment preventative maintenance and cleaning/disinfection as required.
  • Performed various preventative maintenance tasks, quality reports, prototype and special projects involving engineering and quality personnel.
  • Performed preventative maintenance routines utilizing established checklists designed to return the equipment to the original state.
  • Provided on-the spot built-in maintenance services, ensuring first-response for equipment preventative maintenance and failures.
  • Performed setup, calibration, qualification, and preventative maintenance tasks on wafer fabrication equipment.
  • Performed preventative maintenance on production line machinery and completed the daily production logs.
  • Operated lithography tools and performed preventative maintenance to uphold proper factory standards.
  • Performed troubleshooting and preventative maintenance on packaging and granulation lines as needed.
  • Performed monthly preventative maintenance on the automation platform and other lab equipment.
  • Promoted to an Operator Adjuster to perform equipment preventative maintenance task.
  • Performed preventative maintenance on automatic spray machinery and robots.
  • Assisted Maintenance during scheduled Preventative Maintenance and repairs.
  • Performed daily and monthly preventative maintenance checks.
  • Assisted maintenance with preventative maintenance of equipment.
  • Monitor and perform preventative maintenance program.
  • Job duties: Operations and preventative maintenance of Universal and GSM surface mount equipment and MPM screen printers.
  • Ensured tools were ready for production through tool proofing after preventative maintenance was carried out on evaporators.
  • Perform machine set-ups, tool changes, preventative maintenance and routine checks on manufacturing equipment.
  • Perform DNA and steam cell research manufacturing, preventative maintenance and process tool repairs.
  • Implemented a preventative maintenance program that decreased down time by 20%.

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33. Osha

low Demand
Here's how Osha is used in Manufacturing Associate jobs:
  • Achieve compliance with safety requirements and OSHA regulations by monitoring performance and maintaining organized area.
  • Completed manufacturing-related paperwork in accordance with OSHA regulations.
  • Cleaned and maintained supplies, tools, equipment and storage areas in order to ensure compliance with OSHA safety regulations.
  • Adhered to all applicable FAA / OSHA regulations, policies and procedures for health, safety and environmental compliance.
  • Performed on the safety committee representing the Biological glassware department in monthly meetings for OSHA standards and departmental accidents.
  • Completed hours of Personal Protective Equipment training, including respirator fit test, according to OSHA safety standards.
  • Complied with OSHA Safety Requirements encompassing safe usage of chemicals and lock- out, tag- out procedures.
  • Assure that all raw materials are labeled as to chemical toxicities according to OSHA Hazard Communications guidelines.
  • Ensured all vessel pressures and volumes stayed within preset limits as described by OSHA regulated operating instructions.
  • Team Building / Training / Coaching ... Production Flow ... Safety / OSHA ... Equipment Utilization ...
  • Maintained a safe work environment adhering to all state, federal, and OSHA work standards.
  • Maintained a clean and organized work area according to company and OSHA standards.
  • Provided OSHA regulated safety equipment and materials to be used by team members.
  • Adhere to all housekeeping and safety guidelines set by OSHA and company standards.
  • Up kept and maintained the warehouse in compliance with OSHA safety standards.
  • Implemented all safety measures required by OSHA regulations.
  • Followed all company and OSHA health/safety policies.
  • Maintained current awareness of cGMP, DOT, RCRA and OSHA compliance through company training sessions.
  • Work in media prep Clean room, safety, OSHA training
  • Followed OSHA safety guidelines as well as following cGMP regulations.

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34. Inventory Control

low Demand
Here's how Inventory Control is used in Manufacturing Associate jobs:
  • Conducted department safety inspections, held weekly team meetings, and maintained inventory control and facility maintenance.
  • Maintained inventory control of microprocessor and memory with 100% accuracy.
  • Streamlined warehouse for a more effective and efficient inventory control.
  • Performed inventory control while cross-training with Materials Management Dept.
  • Processed daily operations from confidential records for inventory control.
  • Performed quarterly internal audits to insure inventory control.
  • Assisted in materials/supplies inventory control for manufacturing group/labs.
  • Handled inventory control and manufacturing line support.
  • Conducted inventory control required for parts requisitions.
  • Provided inventory audit and inventory control functions.
  • Maintained inventory control and future orders.
  • Worked with inventory control to maintain accurate inventory by checking stock location to verify product and doing inventory counts.
  • Designed inventory control program that increased accuracy from 50% to 99%, and optimized warehouse.
  • Utilized inventory control systems such as AMAPS Data Systems to research, retrieve, and order parts.
  • Coordinated with editorial and inventory control departments to estimate product pricing, quantities, and scheduling.
  • Maintained inventory control of tool storage area to assure a reduction of tool loss.
  • Inventory Control of reagents, chemicals and supplies using proper labeling and computerized transactions.
  • Inventory control / ordering of raw supplies and materials on a weekly basis.
  • Print inventory control tickets from computer system and apply to pallet.
  • Maintained all inventory control for both pilot plant and mid-scale operations.

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35. QA

low Demand
Here's how QA is used in Manufacturing Associate jobs:
  • Perform emergency environmental monitoring if excursion arose, collect data, calculate results and notify QA with any discrepancies.
  • Provided on-site QA representation of contract sterile fill/finish activities of clinical trial material.
  • Cooperated with QA staffs to investigate and timely resolved production deviations.
  • Interacted with QA, QC, Manufacturing Sciences, Engineering, Automation, Validation, Facilities and other support groups.
  • Proposed, worked with Engineering and QA to implement process improvement ideas to standardize and streamline cleaning processes.
  • Performed various cleaning studies and validations on equipment involving multiple departments including Manufacturing, QA, and QC.
  • Performed various testing with QA labs to collect data about the accuracy of various functions of components.
  • Performed the QA function of the service kits and provided training to other co-workers in the process.
  • Collaborated with QA and support groups to investigate discrepancies and provide quick efficient disposition of production batches.
  • Applied appropriate labels to the outside of chassis and the hood *Passed to QA for inspection.
  • Communicate with cross-functional groups: QA, QC and Logistics, to archive GMP goals.
  • Assisted R&D and QA department in maintaining standard and quality in products.
  • Assist QA personnel during Batch Record Review * Gowning qualified in Class 100 environment.
  • Reviewed and approved production records for accuracy and completeness prior to submitting to QA.
  • Keep an attainment of product for the weekly schedule and pull batches for QA.
  • Help QA department with receiving inspection of raw materials when they are backed up.
  • Worked with QA for NCMR disposition, including identifying non-conformance and writing reports.
  • Performed purification training, GAP analysis, and represented group during QA audits.
  • Performed QA status labeling of raw materials, intermediates and finished products.
  • Initiated or closed deviations in conjunction with QA's approval and recommendations.

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36. Final Product

low Demand
Here's how Final Product is used in Manufacturing Associate jobs:
  • Performed Quality Assurance inspections of final product.
  • Handle final product packaging, labeling, and shipping functions, as well as oracle and material allocation needs.
  • Job Duties: Packaging of final products, building and assembly of drainage catheters following schematics and batch records.
  • Perform packaging (vacuum bagging) of final product and prepare paper work for shipments.
  • Performed day to day activity of quality control testing and review of the final products.
  • Operated a cutter press machine where the blank is cut into the final product.
  • Test final product, assemble in cases, and arrange for shipping to customers.
  • Perform multiple tests to determine the durability and reliability of the final product.
  • Inspect final products for manufacturing defects, color variation, and embedded debris.
  • Tracked raw materials, in-process samples, and final products under QC guidelines.
  • Performed Filling, Final Product Packaging, Primary, Secondary and Tertiary Labeling.
  • Participate in the preparation and execution of aseptic fills for final product.
  • Ship final products and sterility samples in conjunction with Quality Assurance.
  • Achieved customer deadlines by packaging final product for shipment.
  • Analyzed data for the optimization of the final product.
  • Packaged final products and shipped them for QC inspections.
  • Perform filtration of buffers and final products.
  • Work with packaging materials to final production.
  • Assemble parts and inspect final products.
  • Prepare in cases the final products.

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37. Uf/Df

low Demand
Here's how Uf/Df is used in Manufacturing Associate jobs:
  • Served as manufacturing lead on Harvest area projects such as UF/DF skid swaps, cassette change outs, and validation activities.
  • Centrifuge production setup* System and feed tank setup and CIP* Column packing and UF/DF filter system setup* Parts cleaning
  • Make kits for processes such as UF/DF, bulk fill, blue process and for fermentation.
  • Qualified on UF/DF skid operations, column packing, and writing SOP's for production use.
  • Performed protein purification, column packing, UF/DF, set up/cleaning column qualifications.
  • Designated as Subject Matter Expert for CIP/SIP, UF/DF operations.
  • Perform purification process using the UF/DF system.
  • Buffer Charging Operations (UF/DF Skids).
  • Perform all downstream unit operations including AKTA Process, KII Ultracentrifuge, and UF/DF system.
  • Executed assembly and disassembly of hoses and filters into column skid and UF/DF skid.
  • Train area operators on Manufacturing Process (UF/DF, Pegylation).
  • Performed filter testing and assisted with UF/DF membrane changeout procedures.
  • Concentrate and dialyze product using UF/DF system.
  • Performed purification using ultrafiltration/diafiltration (UF/DF) processes.
  • Assigned to the Purification Area with the mechanical ability/expertise in Dialfiltration (protein concentration) and Ultrafiltration: UF/DF.
  • Operate 3 UF/DF process', two pre-viral and one post-viral.
  • Performed E.coli Fermentation and Clarification by UF/DF for plasmid DNA production.
  • Performed tasks associated with the UF/DF (Ultrafiltration/Diafiltration) process.

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38. Medical Devices

low Demand
Here's how Medical Devices is used in Manufacturing Associate jobs:
  • Experience in detail oriented work by following federally regulated documents in order to assemble medical devices such as catheters.
  • Operate different equipment and machines that performed the manufacturing of medical devices.
  • Worked with a team of engineers to develop and implement custom packaging for all medical devices created in the company.
  • Worked under the microscope to assemble medical devices in development with the use of visual aids inside a clean room.
  • Assembled, packaged and inspected medical devices in accordance with the quality and production standards established by the organization.
  • Prepare samples; execute mechanical and functional testing on medical devices and R&D development test samples.
  • Analyzed and interpreted blue prints to create medical devices; built product with small tools and microscope.
  • Assisted and train new employees in use of equipment and fundamental processes of manufacturing medical devices.
  • Assembled medical devices according to Assembly Instructions using a variety of hand and power tools.
  • Follow detailed assembly instructions, processes, and procedures to correctly assemble medical devices.
  • Manufacture of medical devices for repair of aortic aneurysms, in a clean-room environment.
  • Assemble medical devices, pack lab bands working with injection molding equipment.
  • Assembled, inspected, and packaged medical devices for supplier shipments and orders
  • Acquired significant knowledge in the setup and assembly of medical devices.
  • Inspected of surgical mesh medical devices and re-work of non-compliant samples.
  • Performed Helium leak tests on laser welded medical devices.
  • Assembled medical devices for medical company called Coherent Performed laser tipping on medical devices.
  • Produced coronary interventional medical devices in a highly regulated environment compliant to ISO 13485.
  • worked on manufacturing line in clean room environment assembling and inspecting medical devices.

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39. Buffer Preparation

low Demand
Here's how Buffer Preparation is used in Manufacturing Associate jobs:
  • Perform skilled operations in a manufacturing setting including Fermentation, Purification, and Buffer Preparation.
  • Gained extensive knowledge of media/buffer preparations, fermentation, formulation, and chemistry conjugation techniques.
  • Utilize laboratory techniques such as buffer preparation, reagent preparation and media preparation.
  • Trained personnel involved with media/buffer preparation.
  • Compound preparing and buffer preparation.
  • Performed nightly buffer preparation, filtration, CIP, SIP of stationary tanks.
  • Prepare components to be used in the purification and buffer preparation areas.
  • Provided training to all new colleagues on buffer preparation procedures.
  • Perform Batch record and Logbooks revision Buffer Preparation and transfer.
  • Performed media and buffer preparation, and support services.
  • Reviewed batch records after media and buffer preparation.
  • Buffer preparation as needed per schedule.
  • Lead role in Buffer preparation.
  • Utilized GMPWork Instructions to perform buffer preparation, execute in-process testing and document production lots generated.
  • Performed cGMP operations related to mammalian cell culture and buffer preparation.
  • Run Pegylation and Buffer Preparation manufacturing process for commercial lots.
  • Certified on applicable SOPs pertaining to Equipment Preparation, Weigh and Dispense, Media and Buffer Preparations.
  • Buffer Preparation: Owned technical side of production processing, monitored critical steps of the production.
  • Buffer Prep Area): Responsible to perform all manufacturing stages at Buffer Preparation Process.
  • Assisted with all prep activities such as pre-weigh of reagents, and buffer preparation.

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40. Pallet Jack

low Demand
Here's how Pallet Jack is used in Manufacturing Associate jobs:
  • Machine Operator./ Pallet Jacket Operator/ General Assembly* Child Care/ Hospitality Aid/ Receptionist* Hospitality./ Customer Service* Assembly Production* Air Tools
  • Use material moving equipment such as pallet jacks, forklifts and dollies to bring products and materials to Supervisors as needed.
  • Utilized forklift, pallet and electrical pallet jacks, air compressed drills, and blueprints.
  • Maintained cleanliness of dock area and organized area using fork lift and pallet jack.
  • Operated pallet jacks, stand up and sit down forklifts, and cherry pickers.
  • Delivered pallets to the warehouse for shipping to individual companies via pallet jack.
  • Organize warehouse and cooler production supplies using forklifts and pallet jacks.
  • Operate material handling equipment such as a pallet jack, etc.
  • Operated forklift, manual pallet jack and electric pallet jack.
  • Used acid fill machines, electric and manual pallet jacks.
  • Packed boxes and stacked them on a pallet jack.
  • Operate forklift and pallet jack maneuvering up to 1000lbs.
  • Assist with pallet jack lifting up to 65 pounds.
  • Certified to use of electric pallet jack called walkies.
  • Use of pallet jack, Assembly of finished parts.
  • Experience driving and handling Forklifts and pallet jacks.
  • Loaded and unload cargo with a pallet jack.
  • Operate fork truck and hand pallet jacks.
  • Scanned incoming packages using hand scanners and placed them on designated pallets Operated pallet jacks to move heavy packages
  • Used the pallet jack to take it around to warehouse.Do hourly bottle checks and fill out paperwork properly.

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41. Customer Specifications

low Demand
Here's how Customer Specifications is used in Manufacturing Associate jobs:
  • Meet quality standards by inscribing identifying information on product and preparing prototype that complies with customer specifications.
  • Understand and interpret specifications that demand meticulous attention to detail and quality to insure customer specifications.
  • Produced various plastic products to meet customer specifications Skilled at the effective operation of various machines
  • Followed clear and defined manufacturing processes in order to ensure compliance with customer specifications.
  • Trained new hires-contractors and insured that quality standards and customer specifications were met.
  • Reviewed work orders to determine raw material requirements and process orders to customer specifications
  • Helped on lamination line assembling layers of material to customer specifications.
  • Achieved customer specifications by packaging products using desiccant and non-desiccant methods.
  • Pressed components into place using press specifies by customer specifications.
  • Build panels using channel and sub-assemblies per customer specifications.
  • Calibrated and tested parts according to customer specifications.
  • Perform post extrusion tasks including cutting to length, re-spooling, printing, sorting product to meet customer specifications.
  • Assembled small and large components to combine servers into racked solution per customer specifications.
  • Used calipers, rulers, and inspection tools to ensure customer specifications.
  • Assembled various models of X86 servers according to customer specifications.
  • Insure each finished board is packed according to customer specifications.
  • Modified parts using table saws to meet customer specifications.
  • Achieved all goals and met stringent customer specifications.
  • Cut rolls of wire to customer specifications.
  • Formulate off the shelf and custom products according to manufacturing instructions Label and package finished goods according to customer specifications

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42. SPC

low Demand
Here's how SPC is used in Manufacturing Associate jobs:
  • Perform or verify quantity of materials required in SAP, WERUM applications to complete filling process and drives SPC.
  • Certified in Documentation Management System, SPC, LOTO, and Ergonomic & Clean room Area.
  • Maintained Statistical Process Charts (SPC), logbooks, and other records as required.
  • Inspect and input data for any SPC Quality Characteristics, flash and cosmetics.
  • Performed ESPC, quality and metallurgical checks on an hourly basis.
  • Worked with manual & computerized SPC charting.
  • Perform daily SPC testing and quality inspection.
  • Certified in SPC, Class 10 &100 clean room protocol, ADI, and ACI.
  • Perform transactions in EBR, SAP and SPC systems.
  • Operate machines *Production sheets *Fill out job traveler *Quality/Quantity checks *Metal finishing *Laser etch *Winspc
  • Increase productivity applying different quality tools, SPC, Lean Manufacturing, Six Sigma, 5S and Kaizen.
  • Used gauges, calipers, go/no go guages, SPC machines, etc to ensure quality.
  • Performed Statistical Process Control (SPC) and also determined Process capability indices.
  • Controlled EDM wire machines Established SPC program knowledge
  • Inspect and analyze defective parts to determine necessary machine adjustments and process improvements Document SPC Track and record daily production logs
  • Operated a CNC machine * Measured all parts for accuracy * Documented all measurements on a SPC chart

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43. Production Goals

low Demand
Here's how Production Goals is used in Manufacturing Associate jobs:
  • Learned and mastered efficient assembly processes, consistently achieving production goals and company quality standards.
  • Recognized by management for achieving aggressive production goals by effectively planning and executing daily schedule.
  • Insured product met quality specifications and daily production goals were achieved.
  • Assemble and wire parts, solder PCB boards, maintain accurate records of production goals.
  • Involved with strategic production planning achieving target production goals to customers request by 98%.
  • Plan and assign tasks to team members in order to meet production goals.
  • Worked with various levels of supervision and engineering to achieve production goals.
  • Can work independently but contribute to the team to meet production goals.
  • Maintain a constant pace with blister filler machine to meet production goals.
  • Graphed various production goals and costumer reports on various software.
  • Maintained daily production goals of 80% of more.
  • Perform equipment change over in accordance with production goals.
  • Led teams to effectively achieve and exceed production goals.
  • Achieved production goals in a cycle time environment.
  • Assisted team in meeting and exceeding production goals.
  • Assure that the production goals are met.
  • Achieved all quality and production goals.
  • Developed and managed all production goals.
  • Attained successful daily production goals.
  • Required endurance and speed in order to keep up with production goals.Worked with a team to ensure customer satisfaction.

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44. GDP

low Demand
Here's how GDP is used in Manufacturing Associate jobs:
  • Generated and maintained up-to-date experimental documentation and records in laboratory notebooks using GDP.
  • Reviewed manufacturing documentation ensuring Good Documentation Practices (GDP) were followed.
  • Prepared media and buffer solutions for the production of bulk drug product in compliance with GDP/GMP guidelines.
  • Monitor and record critical process parameters and data in a timely and accurate manner using GDP's.
  • Record, using GDP, all pertinent operations in production records, logbooks and controlled documents
  • Document with a high level of accuracy and clarity in accordance with GDP.
  • Learned good computer skills and Good Documentation Practice (GDP).
  • Adhered to strict GDP and GMP standards for medical testing supplies.
  • Lead during routine manufacturing activities while ensuring GMP and GDP.
  • Facilitated training in GDP, GMP, and quality procedures.
  • Versed in (GDP) Good Documentation Practices.
  • Followed GMP and GDP regulations.
  • Comply with cGMP practices, regulations and complete manufacturing paperwork following GDP/GMP and documentation requirements.
  • Monitor and record critical process parameters Complete all relevant paperwork following GDP/GMP guidelines.
  • Understand and performing GMPs and GDP in a regular work day.
  • Updated instructions on dozens of SOPs, forms, and other documents to comply with cGDP and create efficient document flow.
  • Ensured strict adherence to cGMPs and cGDPs within the upstream suites on a daily basis.
  • Follow SOPs, GMPs and GDP Great attention to detail and quality of products.
  • Followed and GDP and cGMP in the aseptic purification process of Advate.
  • Maintained cGMP, cGDP and PPE standards

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45. EBR

low Demand
Here's how EBR is used in Manufacturing Associate jobs:
  • Prepare production kits for formulation and filling area anticipating further requirements or schedules changes* Maintain precise documentation in EBR software.
  • Comply with GMP documentation by regularly draft and revise routine documents such as SOP, MP, EBR and technical reports.
  • Generate and complete documents inclusive of SOP worksheets, EBR, Change Controls and deviations.
  • Document work in the EBR system and notebooks according to good documentation practices.
  • Use and Management of the EBR program to annotate product data.
  • Designed and programmed product labels and maintain Zebra label printers.
  • Used taps to clear debris in sheet metal.
  • Experience working with EBR and HMI's.
  • Sweep, mop, and remove debris.
  • Experience in PAS-X 3.1: EBR and EUR documenting Assist in the review of documentation for assigned functions (e.g.
  • Finish product inspection certified EBR (Electronic Batch Record) - Equipment sanitization and sterilization management.
  • Familiarized with PCS, PAS, electronic batch record (EBR) and others industrial softwares.
  • Keep machines and product dust and debris free by vaccumm and cleaning working station.
  • Performed sureFISH and FFPE testing following Work Instructions (WI)/EBR guidelines.
  • Document activities in Electronic Batch Record (EBR) and Werum PAS-X.
  • Perform SAPs and EBR transactions and inform if any discrepancy is found.
  • Loaded lines with raw materials Maintained a clean workspace by breaking down boxes and removing debris from work station
  • Inspected different style's of doors for debris etc.. End Seal Vinyl Sanded different interior parts of door frames Fixed jams

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46. Trackwise

low Demand
Here's how Trackwise is used in Manufacturing Associate jobs:
  • Trained in utilization of TrackWise software for supplier incident and deviation reporting.
  • Interviewed operators and wrote investigations for deviations in TrackWise.
  • Documented deviations in the TrackWise system.
  • Experience performing investigation using the Trackwise System Recognize and accurately report problems.
  • Open an event in the Trackwise system for any detected incident during the process and during batch audit.
  • Created written documentation including SOP's, Trackwise deviation reports, work orders, and OOT reports.
  • Initiated non-conformance reports with Sparta Trackwise software to address process issues.
  • Initiate, investigate, and execute Quality Records using Trackwise.
  • Entered in real time Deviations into Trackwise.
  • Initiate deviations and Lab Exceptions via trackwise.
  • Experienced in Trackwise, data management system.
  • Worked with MES, LIMS, Trackwise, LMS, EDMQ, EDM Teams, and DeltaV software.
  • Use of Syncade eBR, TrackWise, LIMS, and Aspen scheduling software.
  • Worked in a cGMP facility following SOPs and documentation guidelines (using SAP/MERPs, TrackWise, CDMS, etc.)
  • Access to systems such as: Trackwise, EDMQ, Werum, SAP, RTReports and PHA Pro.

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47. Product Quality

low Demand
Here's how Product Quality is used in Manufacturing Associate jobs:
  • Operated automated production machines in wafer fabrication facility, responsible for all aspects of product quality and minor machine maintenance.
  • Maintain production procedures to maintain high standard of manufacturing operations, product quality, reliability, and safety.
  • Tracked lots for product quality and uniformity using high powered microscopes and photo-lithography tools.
  • Collaborated with quality assurance and environmental monitoring to ensure product quality.
  • Innovated operation and record management practices to increase product quality standards.
  • Performed Automatic Capping Machine to ensure product quality.
  • Monitored production operations ensuring product quality and integrity.
  • Demonstrated consistent record of product quality.
  • Followed product quality instructions and safety guidelines
  • Monitor equipment pressures and product quality.
  • Performed product quality architecture checks.
  • Set up and monitored centrifuge processes intended for consistency of flow rates and proper temperature control to ensure product quality.
  • Integrate key business processes to eliminate waste, ensure cost effectiveness, and encourage product quality.
  • Provided guidance and coaching to production operations managers to enable high performance and drive product quality.
  • Assisted supervisory staff in quality control by inspecting welds to maintain product quality.
  • Maintained close relationship with engineers of the process to ensure product quality.
  • Followed all product quality instructions and followed all saftey guidelines.
  • Manufactured Oligo Libraries and perform test to verify product quality.
  • Ensured highest product quality throughout all stages of the manufacturing process by maintaining regular audit checks.
  • Monitored the product quality by a series of tests that measures control and standards specifications.

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48. Sigma

low Demand
Here's how Sigma is used in Manufacturing Associate jobs:
  • Certified trainer on manufacturing processes* Six Sigma/Lean Manufacturing/DMAIC yellow belt certified
  • Facilitated a Lean Six Sigma program for manufacturing floor operations.
  • Participated in lean manufacturing practices and six sigma training.
  • Assisted in implementation and conformance to six-sigma.
  • Practice lean manufacturing/six sigma activities.
  • Collaborate with shop-floor to execute continuous improvement of manufacturing and cleaning processes, using such as Lean and Six Sigma tools.
  • Participated in the implementation of Operational Excellence functions (5s and Six Sigma) in the GMP facility.
  • Served primary functions of leading lean and six sigma process improvement projects in support of production operations.
  • Gained familiarity with LMS and Six Sigma as well as stocked production areas with supplies.
  • Work on Lean Six Sigma Projects to improve efficiency, quality and the manufacturing process.
  • Designated area GMP and Safety auditor - Yellow belt Lean Six Sigma certified.
  • Participated in Lean Six Sigma Program in cell development attaining Green Belt.
  • Trained 40 hours per year to maintain Six Sigma qualifications.
  • Process Improvements ... Six Sigma ... Root Cause Analysis ...
  • Selected to attend Six-sigma Green Belt training.
  • Lean Sigma DMAIC Problem Solving Certificate.
  • Work with government customers to determine areas for process improvement and cost reduction using six sigma methodologies and training.
  • Implemented Lean Manufacturing using 5S, Six Sigma and Kaizen Events for improve for mass production.
  • Apply 5S, Six Sigma and kaizen methodologies to organize and optimize the manufacturing process.
  • Applied 6 sigma methodologies to 12 CIP/PT/SIP SOP revisions to increase operator efficiencies.

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49. New Associates

low Demand
Here's how New Associates is used in Manufacturing Associate jobs:
  • Trained new associates on machine operations and manufacturing procedures.
  • Job duties included training new associates in manufacturing plant, making fiber optic cable, quality control and fork lift operation.
  • On-boarded new associates to the production group and operated in a team-oriented environment focused on training and development of staff.
  • Operated manufacturing tools on a 12 hour Compressed Schedule* Trained new associates on the manufacturing tools in the area.
  • Trained new associates in QC assay procedures, SupersomeTM production (expression, harvest, prep, formulation).
  • Trained and managed at 5 new associates and taught them company value and contributed to their career growth.
  • Subject matter expert (SME) and primary trainer for new associates, supervisors and managers.
  • Provided valuable information leading to more comprehensive solutions in the training of new associates.
  • Train and assist new associates with appropriate work methods for maximum efficiency.
  • Trained new associates on all aspects of the Quality Control process.
  • Cross trained several associates and trained new associates.
  • Trained new associates on all Photo equipment.
  • Trained new associates on material handling processes.
  • Trained new associates on the extrusion lines.
  • Trained new die bonders as On Job Instructor (OJI), improving ramp up time of new associates.
  • Assisted in training new associates in a regulated environment adhering to Good Manufacturing Practices (GMPs).
  • Trained new associates on process operations and appropriate cGMP practices.

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50. R

low Demand
Here's how R is used in Manufacturing Associate jobs:
  • Interacted with senior management of companies in investment universe to obtain input on historical and projected financial performance including earnings estimates.
  • Provide excellent internal and external customer satisfaction by facilitating manufacturing, and assembling vehicle ignition modules on a production line.
  • Participate in process validation studies in conjunction with technical development experts on new product scale-up and process optimization.
  • Created detailed structural designs according to specifications for residential, retail, commercial and industrial projects.
  • Assisted in verification of information recorded on the in-process documents to ensure accuracy.
  • Manufactured sterile product under aseptic conditions in a clinical scale fill-finish facility.
  • Assisted in engineering projects for application and distribution lighting and power systems.
  • Performed manufacturing operations that ensured a quality product was consistently provided.
  • Develop all manufacturing documentation related to formulation, filling and packaging.
  • Controlled inventory from/into stocking locations, following prescribed processes and procedures.
  • Provide support in validation efforts related to the manufacturing processes.
  • Participate in performing process improvement studies with Technical Development department.
  • Board examination on each process before release to manufacturing.
  • Replenished production materials as needed to fulfill daily orders.
  • Document procedures accurately in accordance with GMP requirements.
  • Manufactured die electric micro-chips used in various products.
  • Produced high quality containers intended for pharmaceutical use.
  • Exceeded operational availability goals in multiple positions.
  • Ensured quality of products exceeded customer expectations.
  • Monitor and record critical process parameters.

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20 Most Common Skill for a Manufacturing Associate

Safety Procedures16%
Batch Records9.3%
Cell Culture8.3%
Cgmp Environment7.8%
Assembly Line7.5%
Clean Room Environment5.1%
Cip/Sip4.8%
Raw Materials4.4%

Typical Skill-Sets Required For A Manufacturing Associate

RankSkillPercentage of ResumesPercentage
1
1
Safety Procedures
Safety Procedures
11.2%
11.2%
2
2
Batch Records
Batch Records
6.5%
6.5%
3
3
Cell Culture
Cell Culture
5.8%
5.8%
4
4
Cgmp Environment
Cgmp Environment
5.5%
5.5%
5
5
Assembly Line
Assembly Line
5.2%
5.2%
6
6
Clean Room Environment
Clean Room Environment
3.6%
3.6%
7
7
Cip/Sip
Cip/Sip
3.3%
3.3%
8
8
Raw Materials
Raw Materials
3.1%
3.1%
9
9
Chromatography
Chromatography
3%
3%
10
10
FDA
FDA
2.4%
2.4%
11
11
Aseptic Technique
Aseptic Technique
2.4%
2.4%
12
12
Quality Checks
Quality Checks
2.2%
2.2%
13
13
Troubleshoot
Troubleshoot
2.1%
2.1%
14
14
Quality Standards
Quality Standards
2.1%
2.1%
15
15
ISO
ISO
2%
2%
16
16
Bioreactors
Bioreactors
2%
2%
17
17
Conductivity Meters
Conductivity Meters
2%
2%
18
18
Production Equipment
Production Equipment
1.9%
1.9%
19
19
Protein
Protein
1.9%
1.9%
20
20
Process Equipment
Process Equipment
1.7%
1.7%
21
21
Hand Tools
Hand Tools
1.7%
1.7%
22
22
Production Process
Production Process
1.5%
1.5%
23
23
Ensure Compliance
Ensure Compliance
1.4%
1.4%
24
24
Validation Protocols
Validation Protocols
1.4%
1.4%
25
25
Lims
Lims
1.3%
1.3%
26
26
Set-Up
Set-Up
1.3%
1.3%
27
27
Data Entry
Data Entry
1.3%
1.3%
28
28
Circuit Boards
Circuit Boards
1.3%
1.3%
29
29
Final Inspection
Final Inspection
1.3%
1.3%
30
30
CNC
CNC
1.2%
1.2%
31
31
Capa
Capa
1.2%
1.2%
32
32
Preventative Maintenance
Preventative Maintenance
1.1%
1.1%
33
33
Osha
Osha
1.1%
1.1%
34
34
Inventory Control
Inventory Control
1%
1%
35
35
QA
QA
1%
1%
36
36
Final Product
Final Product
0.9%
0.9%
37
37
Uf/Df
Uf/Df
0.9%
0.9%
38
38
Medical Devices
Medical Devices
0.9%
0.9%
39
39
Buffer Preparation
Buffer Preparation
0.8%
0.8%
40
40
Pallet Jack
Pallet Jack
0.8%
0.8%
41
41
Customer Specifications
Customer Specifications
0.7%
0.7%
42
42
SPC
SPC
0.7%
0.7%
43
43
Production Goals
Production Goals
0.7%
0.7%
44
44
GDP
GDP
0.7%
0.7%
45
45
EBR
EBR
0.7%
0.7%
46
46
Trackwise
Trackwise
0.6%
0.6%
47
47
Product Quality
Product Quality
0.6%
0.6%
48
48
Sigma
Sigma
0.6%
0.6%
49
49
New Associates
New Associates
0.6%
0.6%
50
50
R
R
0.6%
0.6%

15,072 Manufacturing Associate Jobs

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