QC Manager Jobs in New York

Job Title: Quality Management HEDIS/QARR Company: TEKsystems Location: New York City, NY Description: Company: Teksystems Position Title:Quality Management HEDIS/QARR Job Code:2037416 Job Location: New York City, New York Description:Quality Management - HEDIS/QARR Job Description: Our client, a large healthcare organization is looking for a Quality Management Specialist. On a day to day basis candidate will be responsible for:-Coordinate and perform onsite medical record reviews at provider officers -Lead projects for assigned quality measures including the development, implementation, and timely completion of performance improvement initiatives for QARR/HEDIS measures as well as Appendix N contract issues and monitoring regulatory mandates -Monitor provider records and assure compliance with service delivery and quality standards at all times. -Educate providers on all aspects of medical record review criteria including QARR/HEDIS -Collaborate with providers to improve rates for quality improvement indicators and standards of care -Communicate regularly with members, providers and health plan staff To be considered, candidate must have:-2+ years experience with responsibilities listed above.-full knowledge of HEDIS/QARRTo be considered, please forward resume to email address listed. Required Skills for Quality Management - HEDIS/QARR Job: *QUALITY MANAGEMENT * PERFORMANCE IMPROVEMENT * HEDIS * QARR About Aerotek Professional Services: Join Aerotek Professional Services. Our customized employment solutions and personalized approach give job seekers access to great opportunities with competitive salaries. Aerotek offers comprehensive benefits that can include medical, dental, optical, and optional 401k. Don't put your career in the hands of just anyone; put it in the hands of a specialist. Launch or rejuvenate your career today with Aerotek Professional Services! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law. Contact Information Derek T Freitag Apply Now! Begin by filling out the "Apply Online for this Job" section at the top of the page Need Directions? Get office driving directions with Google Maps Register to View Aerotek Professional Services-New York, NY II 757 3rd Ave. Suite 201 New York, NY 10017 TEL: Register to View FAX Register to View

Job Title: Quality Management Coordinator Company: The Execu|Search Group Location: New York, NY Description: Job Title | Quality Management Coordinator Location Compensation Experience Job Type Job ID NYC $70,000-$78,000 / yr 2 year(s) Full-Time J48119 About the Opportunity Ready for a new position? Want to extend your healthcare experience and exposure? As the Quality Management Coordinator for this leading managed care company, you will be responsible for developing, coordinating, implementing and evaluating the continuous quality improvement activities throughout the company. You must possess strong organization skills, the ability to effectively mange time and work independently. If this sounds like you, take advantage of this great opportunity to advance your career by applying today! Company Description Leading Managed Care Company Job Description As the Quality Management Coordinator you will: Design and implement quality improvement studies including selection of valid and reliable indicators and coordinates monitoring and evaluation activities Analyze data and prepare concise, accurate and meaningful quality management reports in accordance with company procedures Participate in intradepartmental quality management improvement teams Coordinate resolution of high level complaints Educate associates about the QM process Assist in defining opportunities for improvement identified through analysis of trends and communicates these appropriately Assist in the preparation for QM related committee meetings Implement, analyze and evaluate the company-wide inter-rater reliability program Prepares QM department responses for RFIs and RFPs Maintain QM documents, case files and correspondence in an organized, confidential and secure manner Conduct, as appropriate, oversight audits for all nationally delegated vendors Develop and maintain ancillary vendor audit tools Communicate significant findings, including potential risk management issues to the AVP Quality Management Assist with coordinating HEDIS improvement activities Assist with coordinating member satisfaction improvement activities Perform other duties as requested or assigned Required Skills RN 2+ years of risk/quality management experience Utilization Review experience in a managed care setting Appeals experience, strongly desired Excellent organizational and time-management skills *

Job Title: Assistant Director of Quality Management/Health Information Company: ArchCare Location: New York, NY Description: To assist the Administrator by designing, correlating and evaluating the facility wide quality measurement and improvement program.  To assist the Administrator to ensure compliance with Federal, State, and JCAHO regulations and standards with respect to preparation and submission of required forms.  To work in cooperative and collaborative relationship with all department heads in regard to quality measurement and improvement program.  To assist training of staff. The Privacy Officer is responsible for overseeing the Nursing Home’s response to Resident/Patient requests to the privacy of their protected health information.  The Privacy Officer also oversees the Nursing Home’s response to court and administrative orders, or requests by law enforcements officers, seeking access to records that may contain protected health information. Responsibilities: Acts as HIPAA Privacy/Security Officer.  Oversees the planning, coordinating and directing of the facility-wide HIPAA Programs.  Facilitates facility-wide education and training for HIPAA. Risk Management.  Interfaces with the facility’s legal department and outside attorneys, insurance companies, and other agencies.  Directs the regulatory component of the risk management process, ensuring that identification, analysis, treatment and evaluation of risk is performed. Quality Improvement Program.  Directs the planning and coordinating of the facility-wide Quality Improvement Program.  Integrates web-based measurement system into the facility-wide QI Programs. Medical records.  Directs and plans the Health Information Management Department, activities and services. Interfaces with regulatory agencies to coordinate availability of medical records for audits and case reviews. Designs systems for medical record analysis and organization for diagnostic coding to support billing/reimbursement.Respond to resident call bell and refer resident and family requests to appropriate health care team member.Develop tools for monitoring and data analysis as needed. Collects monthly reports regarding physical and chemical restraints, pressure ulcer development and healing, and incident reports, customer satisfaction surveys and infection control to assess trends and patterns. Assist team in setting realistic goals.Tracks status of identified improvement to assure goals are achieved.Reassesses goals and plans new improvements if needed.Maintain confidentiality of all work related activities.Communicate all current trends and changes in industry to Kateri staff.Suggest improvements, logs, tracks, and prepare quarterly reports for responses from the facility suggestion box. Compile, date, analyze and identify areas of improvement based on customer satisfaction surveys and all other surveys as needed.Develop auditing programs to meet the needs of the facility.Performs audits in a timely manner.Identify problematic areas for immediate follow-up.Communicate audit results in a clear and concise manner.Responsible for all other duties as assigned.Supervise Medical Record’s Clerk.Ensure established policies and procedures for the Medical Records Department are followed by all personnel. Supervise the Medical Record’s Clerk in maintaining a record of authorized information taken from charts/records (i.e. type of information, name of recipient, date and department, etc.)Extract information from records as authorized/required by insurance companies, Medicare, etc. Overseeing the development and implementation of formal written policies relating to the privacy of protected health information. Ensuring that the Nursing Home has and maintains appropriated forms and notices necessary to comply with federal and state health information privacy regulations. Overseeing the development of, and implementation of, standards for limiting the Nursing Home’s uses and disclosures of, and requests for protected health information to the minimum amounts necessary to accomplish the purpose of such uses, disclosures and requests. Overseeing and ensuring the delivery of initial and periodic follow-up privacy training to all employees, volunteers, medical and professional staff, business associates and other appropriate third parties.Respond to Resident/Patient Requests and Request By Third Parties.  Qualifications: Education normally acquired with a masters degree and graduation of an accredited program in nursing licensed by New York  State.  Appropriate administrative and clinical experience in nursing and/or related field.  Experience in long-term care with at least knowledge of Federal, New York State JCAHO Health Code Regulations and Standards.Registered Health Information Technician or Registered Health Information Administrator preferredNew York State License in Registered Professional Nursing A Bachelor’s degree required; Master’s degree preferredA minimum of 2 years as a Director of QI and/or management experience in QI preferredKnowledge of DOH regulations preferredExcellent organizational, analytical, judgment, problem solving and decision making skillsExcellent interpersonal and communication skills

Job Title: QA / QC Manager - Architecture Company: H2M Group Location: Melville, NY Description: H2M, a multidiscipline architectural, engineering, environmental consulting firm seeks a Registered Architect with 15 plus years of experience to provide Code Compliance review and quality control review of construction drawing and specification packages for large and small projects in the tri-state area. Projects range from approximately $50,000 to $25 million in construction cost and span all Use Group and Construction Type categories. The Quality Control Manager will report directly to the Architectural Division Head, and shall be directly responsible for the overall management of department Quality Control systems and procedures. Some specific responsibilities include QA-QC review of all production documents produced within the department, coordination for constructability with MEP and Civil engineering drawings, specification writing for the department, assisting production teams with construction detailing and assisting in the layout of production drawings at project inception. The successful candidate will be responsible to work directly with individual production teams within a group of over 50 architects and structural engineers at the Melville, NY office. Strong interpersonal skills, specification writing, and technical abilities are required.  We offer a comprehensive benefit package including life / health / dental and LTD insurance, 401(k) with matching contributions, cash bonus, tuition reimbursement, FSA and excellent professional development opportunities.  Email resumes to Register to View  LOCAL CANDIDATES WILL BE GIVEN FIRST CONSIDERATION EOE/M/F/D/V www.h2m.com

Job Title: Quality Control Manager Company: TEKsystems Location: Brewster, NY Description: Company: Teksystems Position Title:Quality Control Manager Job Code:2047895 Job Location: Brewster, New York Description:Quality Control Manager Job Description: - Improves upon and maintains quality production program to ensure conformity of purchased material and final products to quality standards.- Revises, maintains and improves the company quality control manual.- Develops and maintains a supplier quality index, utilizing statistical control programs to assure that only high-quality vendors are retained.- Manages a team of 3-5 Quality Inspectors; Conducts training or coordinates for training as needed.- Meets with vendors, customers, quality representatives, and company personnel to discuss and resolve quality problems as required.- Prepares for and represents the company during all audits and inspections.- Prepares all necessary reports as required by customers and staff personnel.- Experience implementing ISO 9001 policies and procedures. Candidate will lead the effort to gain ISO-9001 accreditation. Required Skills for Quality Control Manager Job: *ISO 9001 * MANUFACTURING About Aerotek CE: Join Aerotek CESM, one of the leading providers of engineering and engineering support professionals in North America. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across a number of different industries. We know it's more than just your day-to-day responsibilities that can make or break a job. It's the support you get. That's the reason Aerotek CE offers a variety of benefits including medical, dental, optical, 401k, and many more. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek CE team! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law. Contact Information Michael Schulke Apply Now! Begin by filling out the "Apply Online for this Job" section at the top of the page Need Directions? Get office driving directions with Google Maps Register to View Aerotek CE-Norwalk, CT 40 Richards Avenue Suite 294 Norwalk, CT 06854 TEL: Register to View

Job Title: Quality Manager Company: Chenega Operations Services, L Location: New York, NY Description: CHENEGA OPERATIONS SERVICES, LLCCompany Job Title: Quality ManagerChenega Job Title: Manager, Quality AssuranceClearance: SecretLocation: New York, Alabama, New MexicoReports To: Project ManagerFLSA Status: Full Time/ExemptPrepared Date: 03/10/2010Approved Date: 03/10/2010 Contingent on Contract AwardSummaryThe Quality Manager will be responsible to the Project Manager for all Quality Control and Quality Assurance for the government project to which assigned. This manager will ensure full compliance with the Statement of Work, all regulatory guidance and company/site policies and procedures. The Quality Manager will manage and supervise the Quality Department consisting of quality/compliance inspectors and will ensure the entire site/project is monitored on a continuous cycle. This manager will report to the Site Project Manager but will also have a dotted line relationship with the Vice President of Operations at Corporate Headquarters. Training records and programs will be maintained in the quality department and will be reviewed on a regular basis to ensure all personnel remain certified to perform the tasks assigned. Essential Duties and Responsibilities Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position1. Manage the operational and fiscal activities of the department to include: staffing levels, budgets, and financial goals. 2. Plan and develop systems and procedures to improve the operating quality and efficiency of the department. 3. Analyze and document business processes and problems. Develop solutions to enhance efficiencies. 4. Coordinate and implement solutions from process analysis and general department projects. 5. Direct staff in the development, analysis, and preparation of reports. 6. Supervise staff in accordance with company policies and procedures. 7. Conduct interviews, hire new staff, and provide employee orientation. 8. Coach and provide career development advice to staff. 9. Establish employee goals and conduct employee performance reviews. 10. Responsible for staff scheduling to include: work assignments/rotations, employee training, employee vacations, employee breaks, overtime assignment, back-up for absent employees, and shift rotations. 11. Assist staff to resolve complex or out of policy operation problems. 12. Schedule and conduct department meetings. 13. Responsible to meet department productivity and quality goals. 14. Communicate with Supervisors, Managers, and Vice Presidents on Department operations. 15. Perform Monthly Safety Training during all hands meetings. 16. Other duties as assigned. SupervisionProvides management and supervision to subordinate managers and supervisors as determined by the organizational structure.Minimum QualificationsTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.Education and/or ExperienceMust have a Bachelors degree in a technical fieldMust have expert knowledge in ISO 9001 Certification as an ISO 9001 lead auditor, is desireableMinimum of 5 years experience in managing a Quality Management program in the Facilities O&M industry in a large scale project of such complexity which requires a high degree of Quality oversight such as, biomedical, nuclear power, R&D, hospital/health careComputer SkillsMust be technically fluent in MicroSoft Products, including Project Management. Certificates, Licenses, Registrations, Clearance: Secret Clearance required.Chenega Corporation is an EOE. AA/M/F/D/V. Native preference under PL 93-638. We participate in the E-Verify Employment Verification Program.*

Job Title: Quality Management Position Company: Jewish Child Care Association Location: New York, NY Description: To ensure the selection and provision of appropriate, effective and quality waiver services to Bridges to Health clients • Coordinate policy changes for programmatic improvement • Collect and analyze data needed to evaluate programs for audits, accreditation, grant evaluations. • Produce reports on accuracy of Medicaid billing and develop and implement corrective action plans when necessary in collaboration with QI and program staff.

Job Title: Director of Quality Company: Company Confidential Location: Buffalo, NY Description: Director of Quality Summary: DTRM Solutions has a great opportunity for an aggressive manufacturing leader who wants to take it to the next level.    The client company has a unparelleled reputation for quality products and quality leadership.  It is looking for the next strong manufacturing leader to be their Director of Quality.  This position is a growth position with succession planning toward a future Vice President within two years. Reporting to the VP of Operations the Director of Quality role will involve creating and/or augmenting the Quality system and programs to be a pro-active vs. a reactive structure. This will involve creating an overall quality vision, setting quality goals and recommend organizational changes to achieve the set goals. The quality head will create consensus and promote quality throughout the company. They will create an environment conducive to continuous quality improvement and implements systems to nurture quality excellence. Communication of the company’s quality system to customers is an essential part of the role. This individual should have hands-on problem solving skills that can be regimented into a failure analysis and preventive measurement process. These processes will be executed by the quality team under the guidance and direction of the Director of Quality.  The Director of Quality will initially need to be involved in typical customer or factory problems at the outset in order to evaluate the challenges within the Quality Department and to develop the necessary programs, and then effectively communicate the vision to the quality team for execution. Responsible for: i) Products Quality and integrity ii) Deployment and maintenance of the Quality Systems iii) Quality verification in all aspects of the operations. Ensure the highest standard of customer satisfaction by delivering the right product to meet or exceed customer expectations.  Oversees Quality Assurance, engineering, Quality Control, failure analysis, receiving inspection as well as Quality document control and compliance. A high level of customer interface is required.  Working with outsourcing partners, some international, is required. Responsibilities Directs, controls and staffs the Quality department to ensure support for execution of Quality systems meets requirements. Continually reviews requirements related to new processes, new products introduction and changes in technology, customer needs and regulations.  Establishes policies and procedures based on ISO9001 and/or ISO14001 standards for all company wide processes and provides training and certification for all employees and processes. Maintains company's conformance to the standards and an internal audit system. Audits outsourcing partners for compliance. Establishes Quality Control plans for all product lines in manufacturing and provides training, inspection and verification tools and schedules verification audits to ensure product assembly, testing and processes conform to the Quality Control plans and instructions. Facilitates and ensures all performance requirements meet specifications and design requirements. Establishes a supplier management program with the materials management team to track Quality of products and on-time-delivery performance of different suppliers. Reviews such findings periodically with the suppliers to communicate their performances and discuss corrective measures, as necessary. Develop metrics for Quality and vendor analysis. Establishes a comprehensive traceability system for product assembly process, supplier materials, components and finished goods shipped to customers. Participates in product and process improvement projects with the design, manufacturing engineering, engineering, sales and production teams.   Establishes a failure analysis system with adequate technical and lab staff to support troubleshooting, root cause analysis, incoming materials failure analysis and failure analysis on customer returns. Ensures reporting and corrective actions are taken in a timely manner. Establishes systems and procedures for containment of non-conforming materials and products throughout the company. Establishes performance goals for product Quality and yields and reviews regularly for cause of deviations and provides guidelines and support for improvements with project based approaches such as design of experiments, statistical tools and capability studies. Get at the root causes of quality issues and fix them by installing a control system. Establishes comprehensive tools, equipment and inspection systems calibration programs and ensures all are compliant.  Set up remote (non-US based) quality systems as required.  Qualifications: Minimum 15 years of hands-on experience in a heavy manufacturing and welding environment, including 5 years of experience in managing the Quality Control function. B.S. degree with experience in manufacturing systems and advanced Quality Systems such as TQM, COO, QIP Familiarity with proven Quality standards a plus (MIL, ISO, SIGMA, ASNT, ASME, ASTM, API, AWS, ANSI, etc.). A proven record in implementing ISO9001 / ISO9014 standards. Knowledge of other quality standards is a plus. Excellent written and verbal communication skills including an ability to develop a consensus and drive all organizations to achieve quality goals. Strong Leadership skills and Team Building Skills. Ability to utilize common software such as Word, Excel, Access, PowerPoint. Ability to learn new software as required. The physical demands described below are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.  Sitting, standing, walking Keyboarding/typing Ability to read effectively from a computer screen and/or paper copy Ability to handle a large volume of work and perform multiple tasks in a fast-paced environment Ability to communicate effectively verbally Ability to work at heights and in adverse weather conditions  The Director of Quality works between an office and plant environment with exposure to varying degrees of heat and noise. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.  This is an equal opportunity employer.

Job Title: Quality Control Manager Company: Location: New York City, NY Description: Position: Quality Control Manager ?Functional Area: Textiles, Apparel, Manufacturing Duration: 12 months (possibility of extension) Number of positions: 2 The position requires an experienced individual with apparel/textile manufacturing background to work as a quality control manager and simultaneously mentor employees in similar work areas.?? Duties & responsibilities: ? Manage the development and implementation of program quality plans, programs and procedures Conduct random quality checks on garments to ensure quality standards are met Ensure that products conform to established company and client standards Monitor the review, analyses and reporting on quality discrepancies Direct investigations of problems and develop corrective actions for recurring discrepancies. Oversee the interface of manufacturing, supply chain management, vendor, subcontractors and customer representatives to ensure requirements are met. Monitors recommendations for corrective actions, dispositions and modifications?? ? Experience: A minimum of 5 years experience in the garment industry and at least three years experience in Quality Control Qualifications: Degree in Manufacturing/Production (apparel-based education). Must have excellent communications skills and a positive attitude. Ability to work in challenging environments. Strong knowledge of apparel/textile manufacturing in countries outside the U.S. Ability to work independently. Please submit your application and update resumes to the following address: Register to View

Job Title: Quality Manager QC Dept. (NY) Company: TEKsystems Location: New Hampton, NY Description: Company: Teksystems Position Title:Quality Manager QC Dept. (NY) Job Code:2036808 Job Location: New Hampton, New York Description:Quality Manager-QC Dept. (NY) Job Description: Our client, is looking for a Quality Manager in the QC Department to work full time, direct placement with the company.On a daily basis, this Quality Manager will be:*responsible for quality functions in the QC Dept*managing the QC Dept*ensuring compliance with the FDA*review and approve specifications and procedures*oversee the batch record reviews*review and approve investigations*issue and Annual Quality Review*oversee customer complaint program*new employee training*coordinate daily activities, oversee instrumentation calibration, and preventative maintenance programs*act as "chemical hygiene officer"*responsible for continuous improvement in all quality processes.To be qualified for this position; the ideal candidate will have a BS or MS degree, MS degree preferred. Also a minimum of 5 years in a QC lab and 3-5 years of Quality management and leadership in the field. Also demonstrate working knowledge of GMP for Food, Feed, or Dietary supplements. Required Skills for Quality Manager-QC Dept. (NY) Job: *QC * GMP * FDA * MANAGEMENT * GLP * TESTING METHODOLOGIES About Aerotek Scientific: Join Aerotek Scientific LLCSM, one of the fastest growing providers of scientific and clinical research services in the nation. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across the scientific and clinical research communities. At Aerotek Scientific, we know it's more than just your day-to-day responsibilities that can make or break a job. It's the support you get. That's the reason Aerotek Scientific offers a variety of benefits including medical, dental, optical, 401k, and many more. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek Scientific team! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law. Contact Information Colleen Sullivan Apply Now! Begin by filling out the "Apply Online for this Job" section at the top of the page Need Directions? Get office driving directions with Google Maps Register to View Aerotek Scientific-Hartford, CT 538 Preston Ave. Suite 310 Meriden, CT 06450 TEL: Register to View