Manufacturing Quality Resume Sample

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Katrine Tillman
888 Kemmer Parkway,  Phoenix,  AZ
+1 (555) 885 1414

Work Experience

Manufacturing Quality Leader
01/2016 - PRESENT
Los Angeles, CA
  • Fosters an environment that promotes Eaton’s goals, philosophies, and encourages continuous improvement through participation and teamwork
  • Well-rounded knowledge in memory product and process in a manufacturing environment
  • Good presentation skills and able to provide high clarity in complex problem solving and business process situation
  • Detailed inspection of products and classification of defects and sorting, packaging and labeling of products for shipment. This requires working with computer systems to record results and get information for processing
  • Also requires following documented techniques/process procedures in operating equipment on the manufacturing floor
  • Assists in the execution of process changes within the manufacturing environment. Produces set-ups and adjustments to equipment or production processes as documented
  • Safety: Identify ergonomic and safety issues and work with the supervisor and other necessary groups that need to be involved to ensure they are addressed in a timely manner. Demonstrate adherence to departmental cleanroom, gowning and environmental procedures on a daily basis
  • Customer Delivery: Maximize throughput without sacrificing quality of the product to meet customer expectations. Meet production goals and be flexible to seamlessly incorporate change of business needs and changing priorities. Schedule driven and understands the prioritization of the workflow
  • Continuous Process Improvement: Awareness and participation in continuous improvement efforts for process/workflow optimization/improvements (i.e., PDCA, Lean Mfg., Six Sigma, 5S) as identified by production supervisor. Identify opportunities for process optimization and increased throughput to supervisor
Manufacturing Quality Inspector
11/2011 - 12/2015
Detroit, MI
  • Leads a team of 15 to 20 Quality profesionals
  • Serves as a EQA and Manufacturing Division subject matter expert in specific Quality systems, technology platforms, regulatory expectations and/or EP management. Utilizes this expertise to drive improved and complaint processes/systems for EQA and Manufacturing Division
  • Assures the development and maintenance of a Quality Agreement with the EP’s. Provides input into the development of contractual agreements with the EP’s
  • Reviews all audit outcomes pertaining to the EP’s and ensures appropriate and timely corrective actions are identified and implemented
  • Monitors efforts to improve the EP’s quality and reliability through ongoing oversight and formal communication programs and forums
  • Provides support to the EP’s to facilitate and validate new product introductions. Provides compliance input and support, as appropriate for implementation of analytical methodology and process development initiatives. In conjunction with other internal MSD departments (ACDS-SAS, GPC, EMT), ensures that EP’s are inspection ready for all new product introductions or transfers
  • Create a champion quality culture in plant
  • Ensure integrity and maintenance of QMS and other related quality metric systems
Manufacturing Quality Intern
08/2004 - 05/2011
Houston, TX
  • Process Stability: Identify and inform supervisor/engineer of issues that contribute or can result in a compromise of quality of the product due to the inability to execute the process in a consistent repetitive manner. Accurate and timely logging of data and tracking
  • Training: Certification achieved and maintained in your owned area of operation. Willingness to participate in initial training/shadowing of peers as identified by supervisor
  • Possess excellent communication skills and attention to detail
  • Ensure team’s compliance with good documentation practices and quality system requirements
  • Study, and analyze plant assembly processes
  • Development and document plant assembly processes
  • Develop Training Materials to include process documentation, visual aids, videos, or other training materials as assigned
  • Flexibility to address special projects as they arise


Missouri University of Science and Technology - Engineering Education Center
1999 - 2003
Engineer's Degree in Manufacturing Engineering

Professional Skills

  • Proven problem solving skills are required
  • Excellent technical, verbal, written and presentations skills
  • Strong communication and interpersonal skills are absolutely essential
  • Strong project management, communications, organization, leadership and interpersonal skills
  • Demonstrated ability to resolve complex technical issues using proven problem solving techniques (8D, Six Sigma etc..)
  • Problem solving skills (ex. 5WHYs, 8D, fishbone, PPS)
  • Good presentation skills and able to provide high clarity in complex problem solving and business process situiation

How to write Manufacturing Quality Resume

Manufacturing Quality role is responsible for leadership, interpersonal, reporting, teamwork, training, database, recruiting, auditing, purchasing, shipping.
To write great resume for manufacturing quality job, your resume must include:

  • Your contact information
  • Work experience
  • Education
  • Skill listing

Contact Information For Manufacturing Quality Resume

The section contact information is important in your manufacturing quality resume. The recruiter has to be able to contact you ASAP if they like to offer you the job. This is why you need to provide your:

  • First and last name
  • Email
  • Telephone number

Work Experience in Your Manufacturing Quality Resume

The section work experience is an essential part of your manufacturing quality resume. It’s the one thing the recruiter really cares about and pays the most attention to.
This section, however, is not just a list of your previous manufacturing quality responsibilities. It's meant to present you as a wholesome candidate by showcasing your relevant accomplishments and should be tailored specifically to the particular manufacturing quality position you're applying to. The work experience section should be the detailed summary of your latest 3 or 4 positions.

Representative Manufacturing Quality resume experience can include:

  • Exceptional interpersonal skills and proven track record of teamwork, adaptability, innovation and initiative required
  • Excellent verbal and written communication skill at all levels of the organization
  • Teamwork oriented, self-starter, leadership skills
  • Manufacturing knowledge or experience
  • Experience working with and or managing teams using and converting technical data into customer presentations
  • Experience working with and or managing teams using and converting technical data into customer presentations

Education on a Manufacturing Quality Resume

Make sure to make education a priority on your manufacturing quality resume. If you’ve been working for a few years and have a few solid positions to show, put your education after your manufacturing quality experience. For example, if you have a Ph.D in Neuroscience and a Master's in the same sphere, just list your Ph.D. Besides the doctorate, Master’s degrees go next, followed by Bachelor’s and finally, Associate’s degree.

Additional details to include:

  • School you graduated from
  • Major/ minor
  • Year of graduation
  • Location of school

These are the four additional pieces of information you should mention when listing your education on your resume.

Professional Skills in Manufacturing Quality Resume

When listing skills on your manufacturing quality resume, remember always to be honest about your level of ability. Include the Skills section after experience.

Present the most important skills in your resume, there's a list of typical manufacturing quality skills:

  • Possesses good mechanical skills to handle lab equipment
  • Good oral and written communication skills (English and Spanish). Fully Bi-lingual
  • Sharp eye for error and strong problem solving skills
  • Work effectively within a global team spanning multiple countries and cultures
  • Works well as part of a team; supports others and communicates effectively
  • Fluent in written and oral English communication skills

List of Typical Experience For a Manufacturing Quality Resume


Experience For Manufacturing Quality Inspector Resume

  • Flexibility by effective transition to changing priorities and ability to adjust to shift changes/work hours as required to meet business requirements
  • Ensure traceability requirements are effectively implemented and maintained
  • Ensure effective implementation of ECO’s into the production process
  • Proven ability to lead teams and work cross functionally to deliver results and drive quality culture change
  • Perform review and approval of validation documents
  • Pharmaceutical, Medical Device, OTC Drug, Cosmetic, and/or Food & Dietary Supplements industry experience is required
  • Management Experience in Organization and People Development

Experience For Manufacturing Quality Technician Resume

  • Operates in a safe and efficient manner and in compliance within our Q.O. Safety and Health Policy
  • Inspection of in-process, finished goods and other samples for distribution
  • Zero (0) to two (2) years of work related experience in a Medical Device or Pharmaceutical environment
  • Communicating and providing feedback to plant
  • Drive Plant Quality metrics including but not limited to: Customer defect rates, Cost of Quality, manufacturing yield and L1L2

Experience For Manufacturing Quality Leader Resume

  • Collects file samples, stability testing samples, and laboratory samples in accordance with established procedures
  • Adheres to cGMP guidelines, SOP’s and plant policies/guidelines. Assists in monitoring area for cGMP compliance
  • Ownership of all production related non-conformance, including 8D investigation to root cause and CA/PA implementation
  • Author, review and/or approve technical documents including deviations, CAPAs and Change Controls
  • Operation of reliability testing/analysis
  • Data interpretation and reporting
  • Perform inspection activities by collecting data
  • Communicate quality issues with the inspectors and production associates during toolbox meetings

Experience For Manufacturing Quality Supervisor Resume

  • Ensure conformance to the quality standards within the manufacturing processes
  • Perform additional final inspection/EOL test to prevent the flow out of non-conforming parts, and implement containment and firewall activities
  • Conduct and evaluate various product tests, calibration and tests related to product and production
  • Lead all quality reviews with internal and external auditors
  • Be responsible for all first parts inspections
  • Actively support Lean implementation throughout plant, specifically when related to quality
  • Be the process expert for CMM, instrom, ultrasonics, micro hardness
  • Issue and track return material authorizations to customers

Experience For Head of Manufacturing Quality Resume

  • Assist with Under Writers Laboratory and Canadian Standards Association Audits
  • Own and maintain Inspection Report disposition and closure follow up
  • Own and maintain all plant quality statistics (external/internal ppm, scrap, rework, control levels, CAR’s)
  • Communicate all quality metrics to plant and senior level management
  • Perform disposition function for unplanned deviations, be a key member of the change control board and perform risk assessment, work with MFG teams on RMA pareto’s and ensure root cause, and ensure that customer requests are being met by MFG teams
  • Highly motivated individual who can work independently and collaboratively across multiple functions

Experience For Director, External Manufacturing Quality Resume

  • Inspects materials, batch record documents and final products during the production process or off line (APQR, re-inspection, batch records). Performs and records release functional and dimensional testing. Restarts automated equipment that stopped for quality issues
  • Evaluates products for defects and recognize unacceptable product. Makes decision regarding product conformity and determines if MQ batch record criteria is met
  • Inputs data (numerical/informational) into batch records, reports and electronic data bases. Recognizes unacceptable product. Monitors production lines for irregularities and reports to area supervisor, accordingly
  • Works with both internal and external customers. Shares information and provides feedback on material, operational, and mechanical related issues
  • Uses good problem solving and interpersonal skills for effective communications. Follows up on activities to ensure quality is maintained. Assists in area improvements, department changes and meetings
  • Follows prescribed uniform and gowning requirements. Maintains a safe, orderly, clean work environment. Reports all accidents to the supervisor. Ensures all PPE (personal protective equipment) is used, as required

Experience For Manufacturing Quality & Reliability Engineer Resume

  • Implement of Ship Holds, containment and release
  • Coordinate initial containment of all non-conformances identified in production
  • Operationalize GA QMS policies/procedures/WI/control for production operations at the site
  • Hosting and preparing for external audits and customer visits, FATs etc.. including agenda’s, scheduling, and resolution of audit findings from external sources
  • Maintain compliance of the production site to all applicable regulatory and quality standards
  • Oversees daily assignments of quality technicians
  • Provide required quality information to assist with customer proposals or enquires

Experience For Manufacturing Quality Intern Resume

  • Comply with EHS regulations & policies
  • Continually identify, recommend and implement process improvements with a LEAN and quality focus
  • Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure that a device conforms to it’s specification and out of specification items are properly handled
  • Knowledge and understanding of Stop Orders, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, as associated with this job type/position
  • Complete all planned Quality & Compliance training within the defined deadlines
  • Inspection readiness activities for global markets
  • Oversight of Contract Manufacturing activities by providing technical project management leadership and Quality oversight for manufacture and release of sterile products

Experience For External Manufacturing Quality Lead Resume

  • Contribute to the creation of regulatory filings and Agency notifications
  • Release of sterile products to global markets
  • Development of monitor/detection for new technology
  • Interaction with requestor from customers and Fab operation for issue/RMA/event and failure analysis
  • Coordinate project activities and output
  • Per 8 hours shift (stand 8 hours, sit 2 hours, and walk 1hour) occasionally bend, squat, climb, reach above shoulder level, kneel, balance and push or pull objects
  • Read and understand blueprints, advanced math skills, communicate (written and Verbal) effectively with other people, learn and understand work instructions, retain knowledge, and advanced understanding of computer work stations
  • Conduct evaluations and oversight of production personnel and processes to ensure procedures are being followed in accordance with GMP compliance and regulatory guidelines
  • Direct manufacturing staff to uphold quality and determine when manufacturing lines need to be shut down to investigate production issues

Experience For Backend Manufacturing Quality Senior Engineer Resume

  • Provide daily supervision of MQ employees & QA Specialists (where applicable) working on a specific shift
  • Implement process improvements with a focus on quality processes
  • Assure that the appropriate resources are utilized on a specific shift as they relate to CAPAs, root cause analysis, preventive actions, trending results and corrective actions, in accordance with facility standards and cGMP compliance
  • Work in conjunction with management to ensure that all aspects related to site cGMP compliance are followed by employees
  • Work with the MQ Manager to ensure that all manufacturing and control procedures and specifications are followed as they relate to production, processes and equipment
  • Experience with GMPs and in compliance driven environment with FDA and regulatory body experience
  • Available to work off-shifts and/or weekends
  • Collect and prepare data identifying root causes of problems and implement corrective action, both and long-term, upon approval of Quality/Design and Manufacturing Engineering departments

List of Typical Skills For a Manufacturing Quality Resume


Skills For Manufacturing Quality Inspector Resume

  • Understanding of process validation requirements
  • Experience in sterile manufacturing and an understanding of the sterilization process and its impact to products
  • Coordinate and facilitate finished goods audits, documenting results and driving corrective action, if required
  • Experience with automotive specific manufacturing quality systems: TS16949 and ISO9001
  • Experience and knowledge in process, product, device or reliability engineering
  • Preferable with over 2 years experience in Integration/ Product engineering would be advantageous
  • Experience working in Quality
  • Experience/training with ISO/TS 16949 environments
  • Related experience in a Manufacturing environment

Skills For Manufacturing Quality Technician Resume

  • Strong understanding of HP’s policies and processes
  • Previous experience in sterile pharmaceutical/vaccine/biologic drug product manufacturing is required
  • A good working knowledge of Lean and or six sigma techniques would be an advantage
  • Experience in leading a work team
  • Ensure validation/verification of all production related equipment including calibration and required maintenance
  • Some years leadership experience in a technically focused manufacturing environment
  • Previous experience in a quality function responsibility
  • Good knowledge in product audits, and process audit
  • Knowledge of development, validation and manufacture of medical devices

Skills For Manufacturing Quality Leader Resume

  • Experience with electro-mechanical equipment recommended
  • Drive quality event to closure and follow up the effectiveness of corrective and preventive actions
  • Demonstrated attention to details and accuracy required
  • Experience with core quality tools (ex. PPAP, PCR, SPC)
  • Working knowledge of environmental monitoring, aseptic manufacturing in a clean room environment desirable
  • Walking and climbing stairs
  • Tagging and de-tagging of discrepant material

Skills For Manufacturing Quality Supervisor Resume

  • Developing OQA quality improvement project
  • Understanding of GKN driveline products and processes
  • Entering collected data into an electronic file or database
  • Maintaining cleanliness and organization of work areas (5s)
  • Support abnormal part handling activities relating to manufacturing. Escalate process concerns to engineering
  • Support abnormal part handling activities relating to manufacturing.Escalate process concerns to engineering
  • Support the Quality manufacturing team across North America with the system analysis, design, programming, testing, and documentation for Q Mobile program
  • Knowledge of machining, assembly, engineering, and manufacturing processes
  • Monitor product quality, measuring key characteristics of a process by sampling parts and analyzing trends

Skills For Head of Manufacturing Quality Resume

  • Supports operations by preparing Certifications of Compliance for manufacturing lots
  • Performs testing on commodities and final product and determines acceptance according to specifications
  • Oversee incoming inspection of materials and disposition of non conforming materials
  • Frequent lifting and carrying (frequently 0- 10 lbs and occasionally 11-50lbs)
  • Provide input and decision making for quality on the shop floor with regard to manufacturing and deviations. Provide corrective action as necessary
  • Work closely with Manufacturing and other support functions to troubleshoot during unexpected events
  • Supervises quality personnel and activities associated with production processes through manufacturing and packaging
  • Support Contract Manufacturing sites, driving compliance & quality improvement initiatives

Skills For Director, External Manufacturing Quality Resume

  • Represent QA on project and improvement teams by guiding/setting quality and compliance requirements
  • Does the right thing; Trusts people to do their job
  • Develops performance; Focuses on problem solving and CI
  • Support Quality and larger Manufacturing teams as needed with additional projects
  • Quality Systems Auditor training required
  • Preference Lead/Internal Auditor training/certification (i.e. ASQ, IATF, RAB, etc.)
  • Adapts positively to a changing environment and/or situation

Skills For Manufacturing Quality & Reliability Engineer Resume

  • Work around and close to moving equipment
  • Red tag and remove all products and materials that fail to meet specifications from manufacturing
  • Lean Principles, Continuous Improvement, or Six Sigma training
  • Perform process and product audits, verification or evaluation of a manufacturing or test operation against procedures
  • Monitors measurement and test equipment to ensure proper identification, status, handling and storage
  • Perform verification of random sampling of final product and related documentation package to confirm compliance and release for shipment
  • Refers to applicable quality procedures and or specifications for the verification of incoming raw materials

Skills For Manufacturing Quality Intern Resume

  • Educate and instruct the plant in quality control testing and operational procedures
  • Own and Maintain compliance for calibration of all measuring instruments
  • Well rounded knowledge in memory product and process in a manufacturing environment
  • Responsible for the integrity of the NPI production related processes including but not limited to pilot runs
  • Drive & co-ordinate L1/L2 for the site including workouts, documentation, and action plan

Skills For External Manufacturing Quality Lead Resume

  • Responsible for the completion and documentation of all production related internal audits including out of Box audits and process audits
  • Assist in resolving product holds, screen stocks, and deviation requests
  • Understand the total quality control concepts, inspection methods, data collection, application of sampling plans, quality cost and quality audits
  • Utilizes Quality Engineering concepts to identify needed improvements in process and product quality
  • Assures proper GMP compliance for the testing facilities, equipment and procedures
  • Discard or reject products, material and equipment not meeting specifications
  • Manage tracking and timely closure of Contract Manufacturer audit observations

Skills For Backend Manufacturing Quality Senior Engineer Resume

  • Detailed working knowledge of cGMP requirements and current FDA enforcement issues is required
  • Participate in problem solving activities to support internal and customer concerns resolution and reduce cost of poor quality
  • Implement and continuously improve the Quality System structure covering all operations
  • Develop and revise standard operation procedures and working instructions in accordance to regulations, Quality Policy and Quality Manual
  • Implement and maintain an efficient system for managing product quality complaints and ensure timely responses to customer
  • Follow established processes unless otherwise instructed by the shift supervisor, tech or engineering related to experimental requests
  • Six Sigma qualification (Green Belt or Black Belt)
  • Is self-aware and aware of others

List of Typical Responsibilities For a Manufacturing Quality Resume


Responsibilities For Manufacturing Quality Inspector Resume

  • Analyze non-conforming product and process performances per engineering and supplier specifications and communicate results to the Plant Quality Manager or appropriate supervision
  • Prepare inspection plans, train new technicians and evaluate quality cost
  • The Quality Technician helps collect data or measure parts to confirm whether or not they meet specifications, and provides information needed for supplier quality or purchasing to communicate the nonconformance with the suppliers or component areas
  • Drive down scrap and rework costs by participating in data driven improvement projects
  • Track and report on data for metrics maintained on the glass wall or management review meetings
  • Provide technical assistance to other departments in resolution of problems detected using the 6-Step improvement model or the 8 disciplines of problem solving methodology
  • Provide support to quality analysts and quality engineers on improvement or cost reduction projects

Responsibilities For Manufacturing Quality Technician Resume

  • ASQ Certified Quality Technician
  • Experience using complex tools, such as accelerometers, calibrated resistance measuring equipment, gauges or inspection fixtures, integrated circuit testers, etc. helpful
  • Experience in blueprint reading required
  • Evaluates deviation and complaint data for undesirable trends. Writes reports and makes recommendations based on these evaluations
  • Participates in the investigation and action taken for deviations. Manages timely completion of investigations to support production operations
  • Maintains QA databases for QA activities
  • Competence in college level chemistry/mathematics
  • Inspect, test, or measure materials, products, installations and work for conformance to specifications

Responsibilities For Manufacturing Quality Leader Resume

  • Lead resolution of process/product non-conformance events
  • Monitor/Report Contract Manufacturer performance metrics
  • Collaborate with J&J business partners and provide batch release when required
  • Develop and implement SOPs, Approve specifications
  • Support the development of methods, procedures, and embedded tests for inspection, testing and evaluation of manufactured products. Maintain related documentation and records
  • Ensure process change requests (PCRs) / deviations are raised where required. Update associated PPAP documentation

Responsibilities For Manufacturing Quality Supervisor Resume

  • Support manufacturing process audits to assess quality capability of the processes against established limits and specifications. Perform additional product quality checks to confirm process capability and stability
  • Support horizontal deployment of lessons learned and countermeasures
  • Serve as the Management Representative
  • Responsible for the implementation and maintenance of all applicable regulations and policies,
  • Develops and executes major quality improvement initiatives in alignment with the subsidiary and site business plans and goal trees
  • Ensure required quality systems and methods are implemented and service conform to all regulatory requirements and internal specifications
  • Perform continuous identification of non-conformities and initiate of corrective and preventive actions
  • Perform periodic Management Reviews on the overall performance of the Quality System and on matters affecting quality and compliance of products and service to executive management to facilitate quality system improvements
  • Knowledge of quality tools, principles and guidelines in the area of quality, lean and six sigma

Responsibilities For Head of Manufacturing Quality Resume

  • Knowledge of the Quality Policy, and the systems and processes described in those documents and which are relevant for your area of responsibility
  • Knowledge of the relevant sections of ISO 9100 (also new revision)
  • SUS Certificate System Administrator. C of T and C of Q Global System Administer: Includes Design of new and Update labels, Access control, System maintenance and Label release
  • Embrace additional responsibilities and extend expertise to other work groups as identified by supervisor
  • Accuracy in communication (verbal and written), generation and interpretation of SOP's/WI's/production documentation for shift pass downs and/or shift meetings

Responsibilities For Director, External Manufacturing Quality Resume

  • Leads a team of 15 to 20 Quality professionals
  • Serves as a EQA and subject matter expert in specific Quality systems, technology platforms, regulatory expectations and/or EP management. Utilizes this expertise to drive improved and complaint processes/systems for EQA and our own sites
  • Closely collaborates with appropriate business and operations areas to achieve our objectives
  • Stand up to 8 to 10 hours
  • Sit up to 2 to 4 hours
  • Occasionally lift a maximum of 20 pounds 3 times per shift

Responsibilities For Manufacturing Quality & Reliability Engineer Resume

  • Record the results of their inspections through test reports
  • Report inspection and test data
  • Team player with the ability to interface responsibly with people at all levels
  • Collect data, establish facts and report non-conformities to supervisor in a timely fashion
  • Computer literacy in necessary software
  • Interpretation of drawings and technical specifications
  • Knowledge of GMP`s and ISO standards

Responsibilities For Manufacturing Quality Intern Resume

  • Computer Oriented. Basic/Intermediate knowledge of Ms Word & Excel
  • Read, analyze, and interpret business policies, technical procedures and specifications, or government regulations
  • Provide solution to a variety of technical problems of moderate scope and complexity
  • Monitors and facilitates the statistical process control activities within assigned areas
  • Prepares and submits reports of non-conformances
  • Perform verification of product integrity test results for conformance and release of products

Responsibilities For External Manufacturing Quality Lead Resume

  • Records, analyzes and reports data for component / product qualifications
  • Issues revisions to forms, specifications ands procedures
  • Conduct lot file reviews when customer complaints are generated
  • Assures accuracy and completeness of products by receiving and reviewing documentation processed at Pall Life Sciences (PLS), notifying documentation originator when errors and shortage of data are detected, and referring to area Supervisor for correction in a timely manner
  • Prepares release for shipping products in the MAPICS System and provides a release form to quarantine area personnel for products by determining if lot reviews have been completed and all release requirements have been met
  • Complies with customer requirements by assisting to Open Order meetings where shipping priorities of the week are established in coordination with Customer Service and Operations Departments, in addition to assisting the CAPA follow up meetings as required by Manager

Responsibilities For Backend Manufacturing Quality Senior Engineer Resume

  • Assures quality by avoiding further processing of all products submitted through the Non Conformance System until proper disposition and performs audits to these designated CAPA areas on a regular basis
  • Assures required documents for product release and additional information required for POR evaluations are received in a timely manner by maintaining effective and continuous communication within all company levels, including external contractors
  • Product Label System Administer: Includes Design of new and Update of labels, Access control, System maintenance and Label release
  • Certificate System Administrator. C of T and C of Q Global System Administer: Includes Design of new and Update labels, Access control, System maintenance and Label release
  • Industry experience (GMP) and previous experience as a people manger are also required
  • Good working knowledge of GMP/GLP and or medical device manufacturing from the Pharma, biotech, medical science or food industries
  • Create and program queries for label and certificate COR investigation for traceability

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