Description:
The Mission Assurance Manager (MA) will be responsible for the implementation and management of the ISO 9001:2000/AS9100 Quality Management System across multiple sites. The position requires a strong knowledge of quality management systems, quality engineering techniques, and Mission Assurance planning and protocol. The Mission Assurance planning and protocol includes the analysis of risk mitigation, leading for continuous improvement, and design, and analysis of process effectiveness. Candidate must be able to effectively collect, analyze, organize and present data to senior management. Interpersonal skills include the ability to effectively communicate within all levels of the company with special emphasis on technical personnel, upper management and with external customers. Manage all Hardware and Software Quality activites across the company. Development of metrics to monitor, measure, and analyze Quality Management System effectiveness with the goal of driving continual process improvements. Establishment of a strong Qualaity Management System that emphasizes prevention of defects by use of Up-front Quality Planning Techniques, Process Action Teams, Employee Empowerment and a Strong Quality Ethic. Management of the direct and indirect budgets. Support proposal efforts to identify and access the contract requirements against the company's existing capabilities. Maintain the ISO 9001:2000/AS9100 Quality Management System certifications. Participation in design reviews, design documentation and verification/validation testing activities. Act as the main interface with the customers, subcontractors and suppliers on all quality related matters. Manage all inspection activities. Manage the calibration and customer/government property programs. Security Clearance Required.
Description:
Candidate must have an understanding of regulatory requirements within the food processing industry, ability to perform standard laboratory testing and analysis procedures, strong communication skills, as well as knowledge about food plant safety. Responsibilities will include overall assurance of product quality and safety; formalize and implement policies and procedures related to food plant safety and laboratory procedures; direct production and sanitation personnel to assure that policies and procedures are adhered to; conduct routine safety and QA audits; represent company during customer and regulatory inspections; maintain formulas, ingredient statements, nutrition facts-making adjustments as necessary to meet customer satisfaction.
Applicant will need the ability to communicate effectively either verbally or written with all levels of employees as well as customers and regulatory agencies; Ability to follow company guidelines and work with peers to achieve the overall goals of the company.
Degree in chemistry, biology, micro-biology or food science desired. Experience in dressings and/or sauces and/or condiments both hot and cold fill desired.
NO RECRUITERS!
Description:
Company: Aetna Location: US-MD-Linthicum Loading Map... Base Pay: $50,000 - $70,000 /Year Other Pay: Employee Type: Full-Time Industry: Healthcare - Health Services Manages Others: No Job Type: Nurse Reqd Education: 4 Year Degree Reqd Experience: At least 3 year(s) Reqd Travel: Not Specified Relocation Covered: No Reference ID: Register to View 1024 a Contact: Not Available Phone: Not Available Email: Send Email Now Fax: Not Available a company overview Aetnais one of the nations leading diversified health care benefits companies, serving members with information and resources to help them make better informed decisions about their health care. Aetna offers a broad range of traditional and consumer-directed health insurance products and related services, including medical, pharmacy, dental, behavioral health, group life, long-term care and disability plans and medical management capabilities. Our customers include employer groups, individuals, college students, part-time and hourly workers, health plans and government-sponsored plans.Visit our Website Quality Management Consultant Report It job description ABOUT OUR COMPANY We are a company built on excellence. We have a culture that values growth, achievement and diversity and a workplace where your voice can be heard.-Participates in the development and ongoing implementation of QM Work Plan activities. * Improve quality products and services, by using measurement and analysis to process, evaluate and make recommendations to meet QM objectives.* Performs data analysis for HEDIS department. a-Must be knowledgeable regarding HEDIS measures, prefer RN with informatics background a-Will communicate with providers (telephonically and through in-person visits) * Conduct presentations to providers and staff To view aaAetna Nurse Video and read our FAQs aboutabeingaa nurse at Aetna, please go to www.aetna.com, click onaCareers,aExperienced Professionals and SelectaNurses.a Oraclick on the link below: http://www.aetna.com/about-aetna-insurance/aetna-careers/experienced_nursing.html ajob Requirements The highest level of education desired for candidates in this position is a Bachelors degree or equivalent experience. LICENSES AND CERTIFICATIONS * Registered Nurse (RN) is desired * Certified Professional in HealthCare Quality is desired * Certified Business Analysis Professional (CBAP) is desired FUNCTIONAL WORK EXPERIENCE * HEDIS data analysis experience * Informatics background preferred * Nurses: Quality Management * Quality Management: Quality Management* Strong Excel and database knowledge * Excellent communication skills * Ability to prioritze * Strong clinical background desired aWe value leadership, creativity and initiative.a If you share those values and a commitment to excellence and innovation, consider a career with Aetna. We conduct pre-employment drug and background testing. Aetna does not permit the use of tobacco related products or drugs in the workplace. No agencies, please. a Aetna is an Equal Opportunity/Affirmative Action Employer. M/F/D/V Aetna is committed to maintaining an environment in which all employees are treated equitably and given the opportunity within the context of the business to achieve their potential. Aetnas Affirmative Action responsibilities extend to women, minorities, persons with disabilities and veterans. Company policy also provides for equal opportunity for qualified individuals regardless of race, color, sex, national origin, religion, age, disability, veteran status, sexual orientation, gender identity or marital status. No search firms please. a aReport ItPlease refer to job code -J3H2B367Y3K33DZ01TD when responding to this ad.
Description:
ORIGINAL JOB LISTING Audit Manager (Quality Control)Location: Rockville, MDSalary: 110KContact: Bob LucasPhone: Register to View Fax: Register to View Growing public accounting firm seeks CPA current on all FASB and accounting standards to do quality control functions for the firm. Individual can also get involved with outside firm peer review work. Prefer seasoned individual with 10-15 yrs. current or very recent public accounting experience.Date Posted: 03/05/10
Job Title: Senior Director, Quality Management
Company: The Cambridge Group Ltd.
Location: Aspen Hill, MD
Description:
Senior Director, Quality ManagementThe Senior Director, Quality Management will provide guidance and expertise to the company in the interpretation and implementation of manufacturing and quality system regulations applicable to investigational and commercial medical device and drug products. In addition, he/she ensures that SOPs describing internal processes are developed and maintained and that the appropriate quality audits are conducted and responded to in order to maintain compliance with regulations and guidelines. The specific duties assigned to the Director, QM include designing and implementing institutional quality systems and quality programs to ensure sustained GMP/QSR compliance. Manage the oversight of vendors and contractors, including qualification and contract management. Disposition (release/rejection) of components, as well as investigational and commercial finished medical device and drug products. Ensure quality agreements are executed with third-party vendors; oversee compliance with quality agreements. Develop, implement, and maintain policies, systems and procedures describing internal processes for management of quality and compliance with applicable regulations and guidelines. Liaise with Senior Director, Auditing and Monitoring, to plan and manage the conduct of periodic internal audits to assure that departments are meeting regulatory requirements and complying with company requirements. Liaise with Senior Director, Auditing and Monitoring to ensure the timely execution of audit plans to assess and maintain compliance with global manufacturing and quality system regulations for pharmaceuticals and medical devices. Assist in cross functional responsibilities between the company and its contractors and clients. Assure the preparation for, management of and response to regulatory inspections of the company. Serve as the management representative per QSR requirements. Establish and maintain systems to ensure complaints are received, reviewed, evaluated, trended, and documented in a uniform and timely manner. Provide leadership in the coordination and management of any corrections, removals or recalls or other quality related crisis. Present to senior management and others on a regular basis re: GMP/QSR update, trend overview, and other strategic analyses related to GMPs and QSRs. Ensure all required GMP/QSR training requirements are satisfied for the department and relevant company functional areas including but not limited to GMP/QSR foundational training, periodic refresher training, SOP training, and drug GMP and device QSR specific training. Proactively manage a staff of at least 3 FTEs and independent contractors to ensure the department is operating effectively, efficiently, and within budget. Pursuant to the company’s quality policy, assist CCO and senior leadership team with the development of annual quality goals and metrics; develop plans to ensure such goals and metrics are communicated to the organization regularly; analyze performance against goals and metrics. A bachelor’s degree is required; MBA or M.S. strongly preferred. Strong working knowledge of current Good Manufacturing Practice (cGMP) for drugs and finished pharmaceuticals and medical device quality system regulations, audit techniques and government regulatory inspection procedures. 15 to 20 years of experience in a regulated industry. environment, preferably in the global pharmaceutical and medical device industry. Strong project management, leadership, problem solving, and organization skills. Excellent communication skills (written and verbal. Experience working with contract manufacturers and quality agreements is preferred.Proficiency in Microsoft Office applications. Ability to travel up to 30% of the time. The Senior Director, QM will manage several direct reports in the Quality Management department, as well as independent contractors, supporting the drug and medical device businesses.Please refer to job code SD7072 when responding to this ad.
Description:
Director, Quality Management SystemsJob ID: 2136# Positions: 1Location: US-PA-Blue BellPosted Date: 2/1/2010Job Category: Operations SupportCDL Required: NoLifting Required: NoTravel Required: YesApply for this job:* Apply for this jobonline* Refer a friend to this jobMore information about this job:Overview:Company Overview:Henkels & McCoy is one of the largest privately held firms providing project management, engineering, construction, installation, maintenance and training services to utility, commercial, industrial and government customers. We have more than 80 offices strategically located from coast to coast.Position Reports to: Vice President, Information and Performance SystemsLocation: Blue Bell Pa.Direct Reports: TBDPosition Summary:To oversee the implementation of Quality Management System (QMS) for Henkels & McCoy and execution of the organization's long-range strategy regarding Quality. To develop, implement and audit quality policies and processes in compliance with industry standards and client requirements.Primary Outcomes:To develop, implement and maintain the H&M Quality Management System that achieves H&M's strategic and operational Quality goals as established in the H&M strategic planning process.To establish H&M's Quality Management System as a customer and industry recognized value addTo support the H&M regional field operations in the delivery of superior Quality work for the company and customer.Major Job Elements:*Manage the development, implementation, and maintenance of Quality Management System in compliance with applicable industry standards (i.e. ISO).* Work with senior management to strategically develop and align Quality Management System priorities and activities.* Communicate the H&M Quality principles and practices throughout the organization and ensure alignment with strategic objectives and work with regional operations and corporate departments to ensure effective implementation of Quality Management System.* Interface with large clients and work closely with project teams to develop and deploy project specific quality plans that comply with contractual quality requirements and deliver customer satisfaction.* Work closely with Continuous Improvement Managers to integrate quality processes and continuous improvement methodology based on Lean principles and practices focused on customer value, employee engagement, process standardization, built-in-quality, waste elimination, and continuous improvement.* Conduct industry research regarding Quality and Quality Systems to insure Henkels & McCoy's remains current in the area of Quality.Qualifications:Knowledge, Qualifications & Experience*4 year Bachelor's degree* 5 years experience in a Quality Leadership or Quality professional position required* 5 years experience in the construction industry / utility infrastructure a plus* In-depth understanding of quality principles and practices, and industry standards (ISO)* Experience with Continuous Improvement using Lean tools a plus* Experience with Environmental regulatory compliance and management a plusCompetencies & Skills:*Effective Communication (writing, presenting, listening)* Program Management (organizing, planning, executing)* People Skills (coaching, building teams, leading change)* Process deployment (design, training, implementation, control)* Customer Satisfaction(helpful, action-oriented, reliable)Henkels & McCoy, Inc is an Equal Employment Opportunity and Affirmative Action Employer
Description:
My clients have asked me to work on a handful of QC Mgr roles for Biotech companies both in MD and PA. Candidates must have a background in biologics. Very good opportunities with solid companies. Please feel free to send me your resume for consideration.
I look forward to hearing from you
Job Title: Quality Control Manager
Company: Location: Andrews AFB, MD
Description:
ECC - Show all jobs for ECC Quality Control Manager Location Andrews AFB, MD Schedule Full Time Job Responsibilities . Comply with the 100% Plans and Specifications provided by the Government for the Repair/Replacement of Runway 01L/19R in its entirety except items specifically identified in this SOW. Take appropriate action to ensure that work is performed in accordance with contract specifications, pertinent building codes & practices as well as national and local standards . Ensure the implementation of contract documents and plans, actively promoting and supporting the quality control program at project sites . Facilitate quality training for project staff, subcontractors, and any parties required to participate to ensure achievement of exceptional quality standards including developing training content and delivering course information . Ensure the appropriate and required testing program is implemented; evaluate, review, monitor and document results . Inspect and document the receipt of all materials to ensure compliance with contract documents . Facilitate the submittal process, including materials, designs and plans . Ensure that submittals meet the contract and project requirements and are submitted to the client as required and in a timely matter. . Author quality related documentation (reports, logs, and records), completing required information for daily reports and client communications in a timely and accurate manner . Ensure that all documentation is organized and uploaded to the project portal . Ensure implementation of the Three-Phase Control Process in accordance with Company standards and contract requirements . Collaborate with Project Managers to ensure that the Three-Phase Process is integrated into project schedules . Provide oversight to subcontractors, clients, and project team members to ensure that construction activities are completed according to design. . Report quality and safety incidents on the Company Incident Database . Ensure implementation and documentation of corrective actions . Verify implementation and close-out corrective actions . Initiate stop work or re-work in coordination with the project team in circumstances where nonconformance to prescribed work methodologies occurs . Provide mentoring, direction, and subject matter expertise to Quality Control Supervisors and/or junior level staff . As requested, participate in employment interviews and make hiring recommendations . As needed, provide performance feedback regarding junior level staff. . In addition to the accountabilities above, other responsibilities, tasks, and deliverables may be assigned to the incumbent of this position. Basic Qualifications This position requires the following: . The ability to communicate in written and oral formats with diplomacy and tact . An aptitude for exercising independent thinking and reasoning . Demonstrated success in teaching others quality concepts and requirements . Successful leadership of subcontractors and project teams in support of quality endeavors . Competent in using Microsoft Office products, email systems, and Windows . Eight years of work experience in a position directly related to quality control Education A Bachelor's degree in Engineering, Construction Management, Occupational Safety and Health or related field is required. Equivalent combination of education and experience may be substituted for this requirement. Preferred Qualifications . Masters degree in Engineering, Construction Management, Occupational Safety and Health or related field . Previous success in working effectively in a dotted line reporting structure . Familiarity with workplace health and safety concepts . Applicable Certification in Quality . USACE Contractor Quality Management (CQM) Training . Proven ability to use USACE Resident Management System (RMS) . OSHA 30 Hour Construction Certification . HAZWOPER 40 Hour Certification and 8 Hour Refresher Certification . HAZWOPER Supervisor Certification . ACI Certification City: Andrews AFB State: MD Zip: 20762 Country: United States of America Job ID: ecc-IGzE8K6V3MYHFqAP0RGa5tGFdV5GpxZGQ5qnf0wjMgiaaFKgDXKHrFY03YDLdl%2bI70WsjUouXS1c6JsBBgU3AQ%3d%3d Job Channel: USA-MD Business/Mgmt. Posted: 02/11/10
Description:
Quality ManagerLocation: Manassas, VAJob Code: 453# of openings: 1DescriptionBe Part of the Next Generation of FlightAurora Flight Sciences is a leader in unmanned aerial systems, with a fleet of innovative aircraft designed to empower small tactical units, and safeguard our borders. Aurora provides the capabilities and process controls of a large company with the "can do" attitude of a small company.Ifyou feel you are qualified, apply for this position, it could change your future.Job Description:The Virginia Quality Manager is the primary oint of contact on and chief administrator of the AS9100 certified Virginia Quality Management System (QMS). The role encompasses but is not limited to the following expectations:Job Qualifications (basic job description):* Sustain and continuously improve the AS9100 certified QMS. Monitor and analyze customer experiences for facility QMS capabilities, develop strategies for implementation and growth, and tactically manage to successful conclusion. Maintain an effective equipment Calibration program.* Develop, document, and manage the FAA Airworthiness, Quality and Conformity processes associated with our aircraft development programs. Proven experience with and knowledge of 14 CFR 23, 43, 145 and other specifications as may be required. FAA Designated Airworthiness Representative (DAR) preferred.* Develop, document, and manage the Virginia internal audits and FOD prevention program to be effective and productive.* Develop, deploy and continuously improve the variety of performance metrics necessary to an effective QMS and for the programs benefit. Analyze data for trends, etc. and make improvements to processes.* Administration of the assigned inspector resources and the Material Review Board (MRB) as required.* Apply Quality Engineering principles, including statistics and predictive analysis, to conduct failure and/or pre-emptive analysis. Evaluate new products and processes as part of customer-focused design review teams.* Administer the Corrective Action Board (CAB) efficiently as part of an effective Corrective Action/Preventative Action (CAPA) program.* Primary administrator of the corporate quality manual QAM-001.* Establish, maintain, and enhance positive customer and supplier relationships to build a cooperative environment influential to both existing contract performance and new contract negotiations. Responsible to interface with customers and/or suppliers on all AVA quality topics.Aurora Flight Sciences is an Equal Opportunity Employer
Job Title: Material Runner/Quality Control Manager Wanted ASAP
Company: Location: Baltimore, MD
Description:
Expanding residential construction company seeking person to deliver miscellaneous construction materials from our storage warehouse and home depot to various projects. When materials are not needed for delivery applicant will visit various projects and inspect to ensure quality. No consturction experience necessary. Apllicant must have a pick-up truck.