Quality Assistant Jobs in Illinois

Job Title: Air Quality Associate Company: ENVIRON Location: Chicago, IL Description: Job DescriptionENVIRON International Corporation is a leading scientific environmental consulting firm providing a broad range of technical services to both public and private sector clients (see www.environcorp.com). ENVIRON is currently seeking candidates for Air Quality Associate working in their Chicago Loop offices. Duties of this position may include the following: * Performing emissions calculations for industrial sources * Conducting air quality reviews of emissions reduction or control * Preparing major and minor source permit applications * Critically review and interpret federal and state environmental regulations

Job Title: Quality Associate II Company: Baxter Location: Chicago, IL Description: Req ID 40332BRBusiness Title Quality Associate IIBusiness Global QualitySub-Business MD General OfficeCountry United StatesState/Province IllinoisLocation of Position Round Lake, ILShift_ 1stJob Description A quality focused individual whose responsibilities include, but are not limited to, the following:* Write, revise and review SOP's.* Performing audits on processes/procedures to consolidate and streamline them and ensure compliance to regulations/standards, and corporate requirements.* Maintain expertise in quality systems and quality techniques.* Maintain a high level of expertise in current regulatory requirements and technical issues.* Participate in multi-site projects in the role of contributor, coordinator or leader.* Assures training requirements are met and records are up to date.* Assist with the management and distribution of quality indicator data.* Support Medication Delivery during inspections and audits.* Interface with Medication Delivery Business Units, Support Organizations, and Manufacturing facilities as part of the Certificate of Compliance and Quality System development process.Job Requirements * Exceptional organizational skills and ability to plan and implement resolutions to technical problems.* Good written/oral communication/problem solving skills* Good interpersonal/communication/influencing/negotiation skills, with a strong customer focus.* Good project management skills, and ability to drive projects to completion.* Working knowledge of FDA code of federal regulations (820, 210,211), ISO 13485 and other applicable regulations.* Bachelor's degree or equivalent experience in a scientific discipline.* 3-5 years experience in Quality or QC/QA analysis.* Working knowledge of Good Documentation Practices (GDP).Percent Travel Required 0%

Job Title: Quality Associate III Company: Baxter Location: Chicago, IL Description: Req ID 41713BRBusiness Title Quality Associate IIIBusiness Global QualitySub-Business Global ComplianceCountry United StatesState/Province IllinoisLocation of Position Round Lake, ILShift_ 1stJob Description Plan and set direction for multiple concurrent Quality IT projects of varying size or a large program/project that supports several key business processes. Responsible for the quality and delivery of projects and commitments on schedule, using assigned internal/external resources and working in partnership with the Global IT organization. Manage/lead all phases of the project from a Quality function business lead perspective. May be responsible for a small number of direct reports.Specific responsibilities of this position include:* Working closely with IT partners to ensure initiatives are completed on time, on budget, and that they achieve targeted results and benefits* Defining the project scope* Creating project plans and managing the project timeline* Identifying and securing required resources* Developing and managing the project budget* Identifying and resolving project risks and issues* Manage Completion of project documentation and deliverables* Directing teams through all phases of the systems development lifecycle* Ability to grasp new concepts quickly and be able to partner with both business and technical teams a must* Excellent problem solving skills, ability to quickly understand design impact to overall initiative return, exceptional team interpersonal skills, with strong organizational and time management skills* Able to foster teamwork and manage multiple resources without direct reporting relationships; as well as orients team toward goal achievement in a matrix management environment* Works well in high-pressure situations common to a dynamically changing and highly regulated environment* Knowledge of applicable procedures, specifications, regulations and standards* Strong project management skills.* Bachelor's degree in Computer Science or related field preferred and relevant work experience (10+ years)* Information technology and systems development understanding/ experience with validated systems desired* Project leadership (PMI or PMP certification a plus)* Healthcare industry within Regulatory Affairs, R&D or Quality functions* Knowledge of Trackwise system is highly preferred.Job Requirements * Understand scientific strategies and be able to invent new methods or new avenues of investigation.* Good interpersonal/communication/influencing/negation skills.* Good project management skills* Working knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices.* Bachelor's degree in science or engineering; advanced degree in the life sciences, physical sciences or engineering, with Ph.D. is ideal.* Lead Auditor training, ISO Lead Assessor training, with 2-3 years experience in auditing techniques, interpreting regulations and quality systems.* Minimum of 5-8 years of experience in Quality, or related field in the medical products industry.Percent Travel Required 0%

Job Title: Assistant Quality Assurance Manager Company: Hella North America, Inc. Location: Flora, IL Description: JOB SUMMARY Assist in developing through proper planning, organizing, coordinating, and evaluating an overall Quality Management System Program for defect prevention; to define the role of each department in the program; to direct these various efforts; and to measure and report the results.ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.  Other duties may be assigned.1.      Assist in developing and implementing quality standards.2.      Provide methods for auditing and reporting the effectiveness of the program. 3.      Plan, organize, implement and supervise the efforts to perform the above-listed activities using the Strategic Quality Manual as the company policy.4.      Responsible for the overall certification and maintenance of the HEC Quality system to assure compliance to the TS 16949 standards.5.      Responsible for document control of policies and procedures.6.      Provide guidance to Quality Engineers on quality tools and standard format for AQP and continuous quality improvements.7.      Delegate the authority, responsibility and work to personnel capable of performing the tasks of the Quality Assurance Program. 8.      Stimulate and guide department personnel in self-development and toward quality mindedness.         9.      Assist in recommending wage scale or increases.10.    Assist in responsibility for preparation of HEC Flora Quality Assurance department budget.11.    Assist in responsibility for operating the HEC Flora Quality Assurance within approved budgets.12.    Assist in assessing the need of new equipment, prepare cost comparisons and justification and write the CEA/Requisition for their purchase.13.    Assist in purchasing supplies and equipment necessary to carry out the quality function, with the approval of those designated within the company to approve requisitions.14.    Assists all major OEM customers in regards to quality problems; works with customers in analyzing problems; provides visits to major OEM customers to analyze problems or complaints; and works with the Quality representatives of all major OEM customers in their performance of Quality duties.15.    Assists in monitoring Customer Scorecards and establishes action plans to meet or exceed Customer expectations.16.    Assist in providing Plant Quality Reports to Corporate HEC and Hella KG as required.17.    Ensure that process inspection is thorough in all phases of the work and that scrap and rework are held within the company expectations.18.    Ensure that end product or outgoing product quality is maintained and improved and that the company retains its reputation for producing a product of the highest standards.19.    Strives for continuous improvement in performing job duties and responsibilities.