Quality Supervisors supervise and coordinate the work activities by engaging in inspecting and testing the manufactured products and goods. The Quality Supervisor Resume highlights duties such as – reviewing quality assurance instructions, checking assembly specifications, inspecting production schedules, determining methods for conducting inspections and tests, directing workers in QA inspections and testing, training new production staff, reviewing reports and conferring with quality assurance, and performing all other tasks as described to this title.
The Quality Supervisor is supposed to possess the following skills – a thorough knowledge of quality assurance methodologies and procedures, relevant field experience, solid knowledge of regulatory requirements, and relevant technical skills pertaining to the field. A college degree in the relevant field of work is commonly seen on most of the resumes.
Summary : Quality Supervisor will also oversee all aspects of the manufacturing process, including product design and development, production planning, distribution planning, as well as project management.
Skills : Data Entry Sales Machine Operator Management Forklift Operation Injection Molding Project Management Microsoft Office Customer Service Lean Manufacturing.
Description :
Responsible for managing external inspections (FDA, RPDA and AEMPS), compliance programs, and other functions.
Responsible for developing and managing top site compliance risks and providing support mitigate risks.
Supports internal and supplier audit program.
Manages the activities of the QRC department in the Quality organization with responsibility for results in terms of conformance to regulations and Talecris quality policies.
Implements the quality systems procedures in the QRC Department and manages compliance.
Understands and assures conformance to regulations applicable to the QRC Department interfaces with regulators during inspections.
Interacts frequently with internal subordinate supervisors, functional peer and senior group managers.
Experience
10+ Years
Level
Senior
Education
Research Publication
Quality Supervisor/Administrator Resume
Objective : To obtain employment in an established company that will allow me to utilize the skills I already have as well as to learn new skills and continue to improve as an employee. An extremely detail oriented and organized individual and I thrive in a structured work environment.
Skills : Solder Technician.
Description :
Communicate quality control information to all relevant organizational departments, outside vendors, or contractors.
Oversee workers including inspectors, or laboratory workers engaged in testing activities.
Monitor performance of quality control systems to ensure effectiveness and efficiency.
Analyze quality control test results and provide feedback and interpretation to production management or staff.
Create and implement inspection and testing criteria or procedures.
Direct the tracking of defects, test results, or other regularly reported quality control data.
Identify critical points in the manufacturing process and specify sampling procedures to be used at these points.
Identify quality problems or areas for improvement and recommend solutions.
Experience
2-5 Years
Level
Junior
Education
High School Diploma
Quality Supervisor/CMM Programmer Resume
Summary : Motivated, personable, professional with 10 years of manufacturing and quality assurance experience. Talent for quickly mastering any unfamiliar tasks. Considerate and tactful with professionals and non-professionals at all levels. Familiar with handling sensitive, confidential records. Established history of producing, implementing, evaluating, and monitoring various aspects of manufacturing products.
Skills : Microsoft Office.
Description :
Performed internal audit insuring the proper implementation of processes defined by the Control Plan and APQP Manual had been followed as well as standards outlined by ISO/TS 16949, ISO 14001, OHSAS 18001 in preparation for Lear's first TUV Certification Audit.
Performed dimensional analysis using FARO Arm Coordinate Measuring Machine as a part of PPAP.
Responsible for supervision and coordination of work activities of Quality Inspectors and Liaisons.
Contribute to the achievement of quality/management objectives by ensuring that quality policies, procedures, and processes are followed.
Maintain accurate personnel records of training, attendance, payroll hours, performance evaluations and discipline.
Feedback daily defects to management personnel and production employees.
Implemented an IPPM Blitz Process that records and tracks quality issues from all aspects of production, supplier quality, and materials handling to identify key items for improvement.
Recommend measures to improve efficiency as it relates to production methods, equipment performance, and quality of product.
Experience
7-10 Years
Level
Management
Education
Mechanical Engineering
Quality Supervisor/Coordinator Resume
Summary : Quality, Production and Maintenance professional with extensive experience in all aspects of manufacturing. Effective leader with acquired skills, knowledge and practice in lean manufacturing principles as well as in implementing standard operating procedures and value stream mapping. Able to efficiently manage production schedules ensuring compliance within corporate policies, FDA, ISO, UL, OSHA, and DHEC standards. Lean Six Sigma green belt certified.
Skills : Solder Technician.
Description :
Analyze and solve quality problems, select sampling plan applications, prepare procedures, train lab technicians, perform audits, analyze quality costs and other quality data, and apply fundamental statistical methods for process control.
Train and educate lab technicians/production personnel on procedures and systems to maximize efficiency and ensure compliance to regulatory and customer requirements.
Provide technical quality direction to production personnel by tracking production technical data and relating it to customer issues.
Provide Quality guidance and recommendations to the production department for raw material /finished product quality compliance, including operator training on product and process specifications, sampling, and inspection and test methods.
Responsible for the inventory for equipment and supplies.
Conduct capability studies and establishing control limits.
Responsible for tracking and trending data and reporting results through the use of various charts.
Participate in customer audits and third party audits.
Experience
7-10 Years
Level
Consultant
Education
Business Management
Regional Service Quality Supervisor Resume
Objective : As An Quality Supervisor, responsible for ensuring that the manufacturing process meets the quality standards set out by the company. This includes monitoring and managing the quality assurance, quality control, and quality assurance systems.
Communicate to various administrations concerning various manufacturing and quality concerns.
Demonstrated strategies to engage team members and understanding of concepts.
Applied data to drive team members to increase productivity.
Interpreted data from production and quality reports.
Design and deliver continuous improvement ideas.
Conduct observations for implementation, evaluation, and monitor progress of previously implemented concepts.
Communicate to various administrations concerning implemented strategies.
Experience
2-5 Years
Level
Junior
Education
High School Diploma
Production Quality Supervisor Resume
Headline : Over 12 year military veteran who earned several commendations and awards for superior performance. Dedicated to bringing organizations to the next phase of growth and development. Diligent and motivated to improve processes, streamline operations and increase revenue. Management professional versed in the aspects of operations management, from scheduling and finance to production. Possesses exceptional communication, organizational and presentation capabilities.
Skills : CAPA Facilitator PDM Administrator Mechanical Designer Production Experience.
Description :
Responsible for generating document and change control policies and procedures that comply with FDA, ISO and other relevant requirements.
Responsible for the maintenance of the central document control library and related content in compliance to ISO and FDA procedures and standards.
Maintain and manage hard copy and electronic documents including master and history files, management review, and other quality records.
Control ECO workflow cycle across all functions of the company.
Facilitate change control meetings for document change orders, notification of document review prior to meeting, and work with teams to ensure documentation is released on time.
Maintained database systems; regulatory common technical documents, CAPA training and auditing as required.
Evaluated performance and compliance of quality system documentation by performing gap analysis on quality system documentation on an annual basis.
Identify and recommend appropriate systems to aid in compliance of quality system.
Experience
5-7 Years
Level
Executive
Education
Associate Of Science
Quality Supervisor/Coordinator Resume
Summary : Quality, Production and Maintenance professional with extensive experience in all aspects of manufacturing. Effective leader with acquired skills, knowledge and practice in lean manufacturing principles as well as in implementing standard operating procedures and value stream mapping.
Skills : Responsible, reliable, hard working and self motivated.
Description :
Develop, implement and oversee Plant Quality procedures from incoming inspection through outgoing finished product.
Responsible for writing and implementing SOP and quality control procedures as per FDA and ISO standards.
Implement lean manufacturing and 5S principles by leading Kaizen events in Quality and Production.
Perform value stream mapping of material flow and equipment layout for production lines.
Compile and publish weekly and monthly quality reports and charts.
Conduct capability and Quality audits at suppliers' production and manufacturing facilities.
Provide technical assistance in the testing and reporting of new and failed products and equipment.
Responsible for Non-Conformance Process and product through disposition utilizing MRB team.
Experience
7-10 Years
Level
Management
Education
MS in Biology
Quality Supervisor/Quality Engineer Resume
Objective : Dedicated to bringing organizations to the next phase of growth and development. Diligent and motivated to improve processes, streamline operations and increase revenue. Management professional versed in the aspects of operations management, from scheduling and finance to production. Possesses exceptional communication, organizational and presentation capabilities.
Skills : Microsoft Office, Minitab.
Description :
Ensures the guidelines, procedures, specifications and reports in the Quality Manual are executed at the plant level and work with corporate QA to revise or improve as needed.
Ensures that quality standards are maintained and communicated to all plant employees.
Conducts weekly Quality Meetings and follow up on action items and improvements agreed upon.
Maintains and provides access to Quality reference materials as needed, consisting of component standards, design folders, customer specifications, AQL sampling, defect guides, etc.
Monitors new item BOM specifications and revisions for missing and/or incorrect components, and for unclear or conflicting item master instructions, and resolves with corporate Specifications group.
Communicates changes to employees and supervisors.
Maintains new start up approval process and ensure quick resolution of all nonconformance's to specifications.
Experience
2-5 Years
Level
Junior
Education
Certificate Of Completion
Quality Supervisor/Liaison Supervisor Resume
Summary : To be employed by a company that will take advantage of my skills who in return will provide me with opportunities for growth. Manufacturing associates resulting in improved customer relations and resolving issues in a quick and efficient manner. My practical experience, positive attitude, attention to detail, and eagerness to achieve goals will add value to your company through team building, problem solving and improved systems.
Skills : Microsoft Office, Microsoft Project.
Description :
Plastic injection mold process that manufactured television frames and printer components for major electronic customers Quasar, Zenith, Sony, and Canon Printers Acquired value added process from our customer to increase sales by $500,000.
Developed and implemented ISO 9000 quality management system.
Developed and maintained APQP documents for over 60 jobs.
Conducted internal audits that defined areas for improvements in training in the areas of training and document control.
Communicated with customers to discuss and resolve quality issues.
Information received from customers was used for pictorials which defined features that were critical to the customer.
Created a corrective action database to track status and repeat issues.
Maintained all corrective actions at one location which facilitated the tracking of actions for completion and analysis of data.
Experience
10+ Years
Level
Senior
Education
Master of Science
Quality Supervisor/Corporate Trainer Resume
Objective : Hard working, self-motivated, dependable, fast learner, self-sufficient, team player, extremely detail oriented, and takes pride in work. I am willing to work all shifts, all hours, and can be on call as needed.
Skills : Communication, Microsoft Office, Public Speaking, Management, Leadership, Project Management, SAP, Teamwork, Regulatory Compliance.
Description :
Ensure center compliance with quality standards and regulations.
Observe processes and ensure center compliance with all applicable state, federal, and company-designated regulations and that staff performs according to all Standard Operating Procedures.
Ensure shipments meet specifications and requirements and authorize final shipments.
Document and track/trend center quality incidents and follow-up on incidents/errors as required.
Ensure that all supplies and materials ordered meet quality regulations.
Direct the maintenance and calibration of equipment and documentation of procedures.
Oversee execution, documentation, and review of internal and external audits.
Ensure that quality control checks are performed as required and are in acceptable ranges for test reagents.
Experience
2-5 Years
Level
Executive
Education
BS In Biology
Regional Service Quality Supervisor Resume
Summary : Quality Supervisor is responsible for quality assurance and quality control functions. This includes ensuring quality standards are met, preventing product defects, and providing technical support to the company’s products.
SOP implementation, understanding of quality control principles and QA audit function.
Conducted Internal and external quality driven audits.
Prepared investigative reports, filed, and maintained important documents.
Identify regulatory deficiencies and implements immediate corrective action.
Manages workload effectively and regularly, inform management of any issues and shared progress on assigned work activities thru holding weekly status meetings.
Continuous process of setting objectives, assessing progress and providing on-going coaching and feedback to ensure that employees were meeting their objectives and career goals.
Ensure customer needs are appropriately met by shipping to schedule.
Experience
10+ Years
Level
Senior
Education
Computer Science
Quality Supervisor Resume
Objective : Three years of supervisor experience. Five years quality control experience in food and medical device manufacturing, and seven years in plant genetics and molecular biology including extraction, electrophoresis, and polymerase chain reaction. Proficient using a variety of laboratory equipment and robotics. Skilled in team building, team leadership, continuous improvement, training, and problem solving.
Skills : FAA licensed Airframe and Powerplant Technician, Certified Pratt and Whitney J57PW flightline engine operation, Skilled in computer database management histories and supply tracking methods.
Description :
Providing quality consulting at Etimex, a blow molding plastics manufacturer located in Charlotte, NC.
Quality Supervisor Responsible for supervising and coordinating the activities of 21 quality inspectors.
Supervisory activities include creating work schedules to ensure quality coverage for all 3 daily production shifts, including weekends.
And monitoring the time and attendance system to ensure accuracy in reporting hours worked for payroll processing.
Providing on-going training to direct reports in quality assurance procedures to ensure compliance with the ISO 9001:2008 standard.
Lead auditor for performing inspections on injection molding.
Responsible for updating and maintaining QMS manual work instructions and corrective and preventative action logs.
Serving as health and safety liaison; investigating, tracking and reporting safety issues.
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