Quality Assurance Director Jobs in Ohio

Job Title: QA Mgr, Family Service Worker, Teacher, Asst. Teacher Company: COMMUNITY UNITED HEAD START Location: Cleveland, OH Description: childcare Community United Head Start Quality Assurance Mgr Seeking an individual to manage and ensure compliance of Head Start performance standards for our direct-operated and collaborative sites. The compliance areas includes education, social services, health, mental health and disability. Must possess excellent communication skills, ability to conduct continuous site visits, prepare statistical analysis and reports, and identify areas of concern. A related Bachelor's Degree is required along with three years of QA experience. Family Service Worker Responsible for the delivery of social services to families, recruitment and enrollment of children, and parent involvement. Duties include the maintenance of various records and reports as required by Head Start standards. An Associate Degree in Social Services, Mental Health or related field is necessary, Bachelor's preferred. TEACHER Day care experience, Bachelor's degree in ECE or related field is required. ASSISTANT TEACHER Associate degree required, Bachelor's preferred. Must possess a valid drivers license and reliable vehicle with insurance is necessary. Deadline is March 12, 2010. Submit resume to: Register to View App. at www.cuhs.org . A background records check and drug test is required. Community United Head Start and Day Care, Inc. 4600 Carnegie Ave., Cleve 44103, fax: Register to View EOE/AA m/f/d

Job Title: Software QA Manager Company: Cincom Systems, Inc Location: Cincinnati, OH Description: Lead Cincom's quality strategy, planning, development and support activities worldwide Software Quality Assurance Manager You will lead the planning, development, and support of Global Quality strategy, methodology, tools, resources and oversight activities of Cincom’s engineering, development, and support organizations. You will implement repeatable processes that promote building quality in (vs. testing it on) throughout all product development activities. You will ensure that ongoing QA capabilities are robust, effective, and efficient in assuring the quality of Cincom’s global engineering activities and delivered products. You will partner with engineering management; product management / Star Teams; services organizations; IS&TS; internal (and external) testing organizations, and other stakeholders in bringing software development projects to a successful conclusion in support of Cincom’s strategic goals and objectives. You will develop benchmarks, metrics and SLA 's for the testing of products currently being marketed, and you will actively engage in all facets of quality deployment. Key Qualifications Four year Degree in Computer Science, Information Systems, or Artificial Intelligence. Masters Degree or MBA preferred Minimum six (6) years leadership in an application software testing environment or an applicable software Quality Assurance role Thorough familiarity with current automated software testing tools and techniques Experience creating and implementing quality strategies and plans Experience working with offshore companies and outsourcing providers Excellent time management, communication, collaboration, decision-making, human relations, presentation, and organizational skills Superior professional presence and business acumen Able to think outside the box and to work within operating constraints Willingness to travel globally as required, as much as 50% Residence near Cincom’s World Headquarters in Southwest Ohio is required. This is not a work-from-home or telecommuting position. If you are interested in becoming a senior member of the Cincom Global Development and Support engineering leadership team, please APPLY NOW or forward your resume to Register to View Be sure to attach your resume and to reference PRF 3216Y. RESUMES ACCEPTED UNTIL POSITION IS FILLED ...an equal opportunity employer About Cincom Systems Cincom creates and delivers software, tools and services to clients worldwide who need to innovate and simplify complex business processes. Cincom serves thousands of clients on six continents. Cincom’s easy-to-use, high-value software solutions empower clients to overcome operational obstacles, thereby paving the way to higher productivity, sustainability and profits.

Job Title: Quality Assurance Manager (Assistant Manager) Company: Location: Columbus, oh Description: The work of the quality assurance manager will be affected by the nature of the employing organisation but is likely to include some or all of the following activities: - promoting quality achievement and performance improvement throughout the organisation; - working with purchasing staff to establish quality requirements from external suppliers; - monitoring performance by gathering relevant data and producing statistical reports; - setting up and maintaining controls and documentation procedures. Requirements: US resident or valid US work permit. No criminal record. Intermediate to advanced knowledge and experience with MS Word, Excel and Outlook. Excellent communication and organizational skills. Ability to work solely and as part of a team. To Apply: If you are interested in this job please send your resume. We will reply you in 1-2 business days. Memo: We are sending you this offer as you have posted your resume on a job seekers website which provides resume access service. We will not contact you again if not required. E-mail: Register to View -group.biz Salary/Wage: $1,000-1,400 USD Status: Full-time, Part-time • Location: Nationwide • Post ID: 2106308

Job Title: Quality Assurance Manager (Assistant Manager) Company: Location: Toledo, oh Description: The work of the quality assurance manager will be affected by the nature of the employing organisation but is likely to include some or all of the following activities: - promoting quality achievement and performance improvement throughout the organisation; - working with purchasing staff to establish quality requirements from external suppliers; - monitoring performance by gathering relevant data and producing statistical reports; - setting up and maintaining controls and documentation procedures. Requirements: US resident or valid US work permit. No criminal record. Intermediate to advanced knowledge and experience with MS Word, Excel and Outlook. Excellent communication and organizational skills. Ability to work solely and as part of a team. To Apply: If you are interested in this job please send your resume. We will reply you in 1-2 business days. Memo: We are sending you this offer as you have posted your resume on a job seekers website which provides resume access service. We will not contact you again if not required. E-mail: Register to View -group.biz Salary/Wage: $1,000-1,400 USD Status: Full-time, Part-time • Location: Nationwide • Post ID: 1839565

Job Title: Water Treatment Quality Assurance Manager Company: The Ross-Carlisle Group, Inc. Location: Dayton, OH Description: Water Treatment Quality Assurance Manager Locations: Midwest Salary: Commensurate with experience Job ID: 100103 Contact us now to apply for this position Duties: We are the Ross-Carlisle Group, an Ohio based recruiting firm specializing in engineers and other hi-tech and manufacturing professionals. A major manufacturer of industrial water treatment equipment and products has contracted us to conduct a search for a full time/diret-hired Waste Water QA Manager who will plan, manage, and control programs and procedures to maintain an acceptable level of Waste Water Treatment product quality as established by various federal, state, customer, and division requirements. Qualifications: A Bachelor of Science Degree in either mechanical engineering, chemical engineering, or similar program is required for this position, along with 10 plus years of experience within the Waste Water Treatment Processes. Must be a U.S. Citizen or have Permanent Residency/Green Card. Salary/Benefits: Pay is commensurate with experience along with a competitive Benefits Package. Position is located in the Midwestern United States. Contact Info: Email resume to Ron Toke at Register to View or or go to http://www.contactrcg.com or call him at Register to View for more information.

Job Title: Quality Assurance Manager Company: PDSI Technical Services, Inc. Location: Dayton, OH Description: Description: We are currently seeking a Quality Assurance Manager for a client in Dayton, OH. This individual to be responsible for the overall quality of the company. Responsibilities will include developing, implementing, managing, and controlling business procedures and processes. Applicants must have an in-depth understanding of how to implement a formal quality like ISO in an “engineered-to-order” custom system environment. The ideal candidate will have Capital equipment experience. All applicants must have experience with pressure vessels, welding, structural steel, piping spools and electromechanical assembly. Special Requirements: Qualified candidates must have a Bachelors degree and ten plus years quality experience. ISO and Lean Manufacturing experience is required. Business start up experience is a plus. NOTE: Applicant must be presently authorized to work in the United States. This company does not sponsor individuals for the purpose of obtaining H-1 Visas. Unless the body of this posting specifically states otherwise, NO relocation allowance or per diem is available. CANDIDATES WITHIN A REASONABLY COMMUTABLE DISTANCE OF THE ABOVE WORK SITE ARE PREFERRED. HOW TO APPLY: PDSI Technical Services, Inc.     See all jobs in Dayton OH

Job Title: Senior Manager of QA Testing Company: eConsultAmerica Location: Cincinnati, OH Description: eConsultAmerica is a preferred vendor supplier on retainer with worldwide provider of information technology services and business solutions to a broad range of clients. Our client is seeking an experienced and savvy Senior Manager of QA Testing. This position will be based in the continental United States. This position will require 50% - 100% travel with no relocation necessary. If you are interested please forward a brief cover-letter and a update-to-date word-formatted softcopy of your resume, as an attachment, with full contact information (i. e. full name, address, city, state, zip code, telephone number and email address). We will respond back within one business day. US Citizens or Green Card holders only apply. Our client is not considering H1b visa candidates at this time. POSITION DETAILST he Senior Manager of QA/Testing provides consultative support to clients and our client's personnel on integrated projects in a Sr. Consultant capacity. The chosen candidate acts as senior on-site advisor to client and team members. You will play a central and key role in defining the scope of projects, understanding a client's issues/problems, and conceiving client deliverables. Participates in and leads development of both business and QA/testing applications. Knowledge of specific industry trends and key issues and challenges facing a client required. Strong leadership skills, with proven ability to provide clear direction to set matrix resources are required. Experienced in use of PM tools to track all aspects of QA projects are essential in this role. QA/Test activities include: design, develop and execute test strategies/plans debug and troubleshoot perform impact gap analysis coordinate test resources weekly status reporting problem resolution and analysis defect tracking and defect triage activities BEST INDUSTRY - Banking/Financial Services, Healthcare, Insurance, Life Sciences, Manufacturing and Transportation/Logistics BEST DEPARTMENT - ConsultingBachelors Degree is required. Masters Degree or MBA highly preferred. PMP or PMI certification is strongly preferred. Management experience in Consulting is mandatory in this role. Minimum of 3 years at Big-5 Consulting Firm is required. Minimum of 10 years QA/Testing experience is mandatory in this role. 5 years of project budget forecasting and planning of projects of $3. 5 mil or more is required. 5 years experience supervising and managing a team of 4 or more direct reports. 3 years minimum experience in managing, planning, administering and/or executing Quality Assurance (QA) test activities during all test-related project phases, for one or more IT projects. Strong track record of architecting and successfully delivering large-scale project and program initiatives is required. Strong track record of leading design, development and implementation delivery of project and programs is required. Strong Business Process skills are required. Strong self-starter and leadership characteristics and communication skills Exemplary presentation and proposal skills are mandatory in this role. Compensation 110K - 130K .

Job Title: Quality Assurance Manager (Assistant Manager) Company: Location: Akron, oh Description: The work of the quality assurance manager will be affected by the nature of the employing organisation but is likely to include some or all of the following activities: - promoting quality achievement and performance improvement throughout the organisation; - working with purchasing staff to establish quality requirements from external suppliers; - monitoring performance by gathering relevant data and producing statistical reports; - setting up and maintaining controls and documentation procedures. Requirements: US resident or valid US work permit. No criminal record. Intermediate to advanced knowledge and experience with MS Word, Excel and Outlook. Excellent communication and organizational skills. Ability to work solely and as part of a team. To Apply: If you are interested in this job please send your resume. We will reply you in 1-2 business days. Memo: We are sending you this offer as you have posted your resume on a job seekers website which provides resume access service. We will not contact you again if not required. E-mail: Register to View -group.biz Salary/Wage: $1,000-1,400 USD Status: Full-time, Part-time • Location: Nationwide • Post ID: 2257329

Job Title: Quality Assurance Manager Company: Sterling-Hoffman Life Sciences Location: Dublin, OH Description: Our client is a leading biomedical company based in Ohio. They focus on the development and commercialization of surgical and diagnostic products that enhance patient care. Qualifications/Skills Required -------------------------------------------- 1) College degree in Biological Sciences 2) Minimum 5 – 10 years of significant quality assurance experience in manufacturing biopharmaceuticals or pharmaceuticals or equivalent combination of education and experience 3) 5 – 10 years of quality assurance experience in a GMP environment 4) Experience in regression analysis, chemistry and software validation 5) Experience in audits, QMS management and validations 6) Good computer knowledge (word and excel as well as statistical and quality control software applications) 7) Excellent communication, organizational, project management and strong analytical skills and demonstrated attention to detail 8) Ability to focus on solving conflict, maintain confidentiality 9) Ability to listen to others without interrupting, keep emotions under control, remain open to others' ideas and tries new things 10) Ability to speak clearly and persuasively in positive or negative situations, listen, get clarification and respond well to questions 11) Demonstrated group presentation skills combined with willingness to participate in meetings 12) Ability to write clearly and informatively, edit work for spelling and grammar, vary in writing style to meet needs and present numerical data effectively 13) Ability to balance team and individual responsibilities, exhibit objectivity and openness to others' views and put success of team above own interests 14) Ability to always look for ways to improve and promote quality and demonstrate accuracy and thoroughness 15) Ability to understand business implications of decisions and demonstrate knowledge of market and competition 16) Ability to align work with strategic goals, work within approved budget and conserve organizational resources 17) Ability to develop strategies to achieve organizational goals and adapt strategy to changing conditions 18) Demonstrated knowledge of device, drug and biologic GMP, as well as quality and manufacturing responsibilities associated with the US FDA and other international regulatory agencies 19) Ability to read and interpret documents such as regulations, industry standards, blue prints, bills of materials, product, process specifications, safety rules, operating, maintenance instructions and procedure manual 20) Certified Quality Auditor (CQA), Certified Quality Manager (CQM), or Certified Quality Engineer (CQE) 21) Willingness to travel (up to 40% of the time, or as circumstances dictate) Partial Job Description -------------------------------------------- 1) Ensure the continued compliance with integrated Quality Management System and processes 2) Meet the requirements of the regulatory agencies in the US, Europe, Japan, Canada as well as other international regulatory agencies 3) Plan, implement and revise programs and procedures that ensure appropriate practices and standards relevant to the control of device, drug and biological product quality and efficacy 4) Implement all procedures leading to compliant, valid and documented release of device, drug and biologic product by performing the duties 5) Participate in developing and approving validation programs for facilities, manufacturing processes, products, environmental classifications, etc. 6) Maintain quality management system and processes to ensure changes to programs, procedures, and processes are approved and appropriately documented and validated 7) Work with suppliers to ensure that company and supplier facilities pass regulatory inspection(s) 8) Serve as the audit host for all regulatory inspections for company and suppliers 9) Direct audit program to review facility, personnel and equipment qualifications of suppliers 10) Ensure compliance with company and regulatory specifications regarding competence, purity, size, quality and durability 11) Perform audits of products and processes to identify areas for improvement 12) Maintain GMP at company, suppliers and study sites 13) Oversee product complaints, deviations and failure and out-of-specification investigations 14) Provide quality assurance support for regulatory submissions 15) Manage records and disposal of radioactive and bio-hazardous materials 16) Pursue training and development opportunities and strive continuously to build knowledge and skills 17) Share expertise with others 18) Manage difficult or emotional customer situations 19) Respond promptly to customer needs and request for service and assistance 20) Meet commitments 21) Prioritize and plan work activities, use time efficiently, sets goals/objectives and develop realistic action plans. 22) Approach others in a tactful manner, react well under pressure, treat others with respect and consideration regardless of their status or position 23) Accept responsibility for own actions and follow through on commitments 24) Meet productivity standards and complete work in timely manner 25) Observe safety and security procedures and use equipment and materials properly 26) Adapt to changes in the work environment 27) Manage competing demands, change approach or method to best fit the situation and deal with frequent change, delays, or unexpected events 28) Follow instructions, respond to management direction and take responsibility for own actions 29) Undertake self-development activities, seek increased responsibilities, take independent actions and calculated risks 30) Look for and take advantage of opportunities 31) Ask for and offer help when needed 32) Display original thinking and creativity 33) Meet challenges with resourcefulness and generate suggestions for improving work

Job Title: Quality Assurance Manager I Company: Coca Cola Company Location: Columbus, OH Description: Reports to Plant General Manager and provides leadership for the plant's quality organization and serves on the plant's leadership team. Manages and develops quality team leaders / supervisors and quality technicians. Develops the quality assurance department's budget. Oversees quality laboratory operations to ensure that testing of products and ingredients meet specifications. Ensures that quality records are complete and maintained according to Company standards. Coordinates incident management activities at the Plant. Serves as Program Owner for the Plant's Documentation and Record Keeping and Corrective and Preventive Action Programs. Provides leadership for continuous improvement at the Plant and reports quality information as a part of the Management Review. Function Specific Activities:Provide direct reports with leadership, direction, and coaching toachieve work objectives and improve performance and skills.Interpret data from routine and non-routine analyses in order tovalidate that ingredients/materials meet specifications and approve forshipment to Company plants.Review and evaluate reported crisis (i.e., highly-urgent productrelated problem with immediate negative implications for the Company)and formulate a plan of action for handling the incident/issues basedon area of expertise/responsibility.Troubleshoot equipment (e.g., manufacturing, dispensing equipment) bycreating and/or using methods and tools such as Failure ReportingAnalysis and Corrective Action Systems (FRACS) and Mean Time BeforeFailure Analysis to resolve problems, evaluate improvements ordetermine/justify ways to improve efficiency and lifecost.Interact with and inform suppliers, Purchasing, and Company plantsingredient sample analyses, ingredient issues or rejections, and toresolve problems related to ingredient approval.Evaluate a direct report's performance against established performanceexpectations.Review audit results and identify the severity of audit findings orthe risk associated with the findings to ensure the appropriate levelof action is taken to eliminate non-conformance.Track or follow up on corrective action plans in order to ensurecompletion of all items in the specified time frame.Develop and execute facility/product plans to ensure they meet currentand future business requirements (e.g., good manufacturing practice,quality, volume and product growth, regulatory requirements, newproduct introductions, and health and safety).Develop implementation strategies, implement, evaluate and/or certifyeffective implementation of The Coca-Cola Quality System (TCCQS).Education:Bachelor's Degree or equivalent work experienceRelated Work Experience:At least 7 yearsCore Competencies:Drives Innovative Business Improvements:  Develops new insights into solutionsthat result in organizational improvements; promotes a work environment thatfosters creative thinking, innovation and rational risk-taking.Balances Immediate and Long-Term Priorities: Seeks to meet critical objectiveswhile considering the impact of those decisions and activities on the abilityto achieve long-term goals.Delivers Results: Focuses on the critical few objectives that add the mostvalue and channels own and others' energy to consistently deliver results thatmeet or exceed expectations.Imports and Exports Good Ideas:  Relentlessly seeks, shares and adopts ideasand best practices in and outside the Company and embraces change introduced byothers.Develops and Inspires Others:  Builds and maintains relationships thatmotivate, guide, and/or reinforce the performance of others toward goalaccomplishments.  Develops self and others to improve performance in currentrole and to prepare for future roles; seeks and provides feedback and coachingto enhance performance.Lives the Values: Demonstrates the values of The Coca-Cola Company throughwords, actions, and by example; fosters an environment that reflects the valuesof the company.Technical Skills:Document Management: Ability to create, approve, track and filedocuments and records in compliance with The Coca-Cola Quality Systemor other formal guidelines.Food Science: Knowledge of principles and techniques of basic foodscience and their application to the beverage industry.Good Manufacturing Practices: Knowledge of the basic elements of GoodManufacturing Practices. This includes understanding of Company andregulatory (e.g., cGMP, CFR) guidelines.Laboratory Practices: Knowledge and application of Good LaboratoryPractices (e.g., handling of chemicals and glassware, preparation ofstandards and reagents, proper measuring techniques, data management,housekeeping). Honesty and integrity have always been cornerstone values of The Coca-Cola Company.  Our passion for people of integrity mirrors our spirited drive for total quality in our brands.  These and other elements allow the company to sustain strategic practices and drive business performance.  The Personnel Integrity Assurance Program is another step toward making The Coca-Cola Company the premier workplace. This process includes a pre-employment background investigation that applies to all applicants employees and contractors of the company.  The scope of this inquiry may cover such elements as education employment history a criminal history check reference checks and a pre-employment drug screen. Designated countries or sensitive positions within the company may have more stringent standards. At The Coca-Cola Company you can cultivate your career in a challenging and dynamic environment.  We are the largest manufacturer and distributor of nonalcoholic drinks in the world-selling more than 1 billion drinks a day.  Unlock your full potential with a future-focused company that is known and respected throughout the world.