Job Title: EHSQ (Enviromental,Health,Safety,Quality) MANAGER
Company: Robert Scott and Associates
Location: Atlanta, GA
Description:
The Company is a $4-5 Billion International Chemical Manufacturing Company . This position, located in their (Atlanta) North American Headquarters Office, implements and oversees integrated safety, quality and environmental management systems at our North America locations. This is a regional staff position in the EHSQ North America organization which interfaces with all functional departments and manufacturing and logistics sites in North America and with EHSQ overseas. The position serves as liaison with the management systems registrar, inetrfaces with customers, regulators, etc. concerning the management systems, and coordinates all activities associated with gaining and maintaining management systems certification. This position also serves as focus for continual improvement opportunities. Contact Robert Scott at Register to View or Register to View . primary responsibilities and accountabilities of the position are:Develop a comprehensive integrated Mangement System conforming to ISO 9001, ISO 14001 and OHSAS 18001 standardsServe as the Management System Representative for North AmericaDevelop and publish management system documentsConduct management system auditsMainain system files and track action itemsOversee IT Systems related to the function (Document Management, SAP Notifications) Working Experience and Education:Bachelors degree in Chemistry, with Chemical Engineering preferred Minimum 8 years experience in the Chemical Industry, with Health, Safety, Environmental and Quality management Systems is a MUSTCertification Managemnet Systems auditing requiredMinimum 3 years supervisory experience Competencies and Skills Required:Ability to develop and implement systems and conduct trainingProficient with basic MS Office applications (Word, Excel, PowerPoint, Otlouk)Work process analysisRelocation assistance is available for this position.
Description:
Position Purpose: Perform duties to oversee and manage the functions of the quality improvement program. Providing support to staff and communicate with departments and staff to facilitate daily quality improvement (QI) functions. Knowledge/Experience: At least 3 years nursing experience and 1 year of recent quality improvement and supervisory experience in a healthcare environment, preferably managed care. Position Responsibilities: • Review and analyze reports, records and directives. • Confer with staff to obtain data such as new projects, status of work in progress, and problems encountered, required for planning work function activities. Verify data to be submitted in accordance with government program requirements and ensure compliance with state, federal and certification requirements. • Prepare reports and records on work function activities for management. • Oversee the review and analysis of reports. • Evaluate current procedures and practices for accomplishing the assigned work functions objectives to develop and implement improved procedures and practices and to ensure compliance with required standards. • Collaborate with appropriate departments to document, investigate and resolve formal or informal complaints and appeals in accordance with Company and State policies, procedures and requirements. • Monitor and analyze costs and participate in the preparation of the budget. License/Certificates: Current state registered nursing license required. Certified Professional in Healthcare or other licensed clinical experience preferred.
Job Title: Quality Manager America's
Company: Novartis
Location: Atlanta, GA
Description:
Novartis A health care company with global reach.
A product pipeline filled to the brim. A team committed to
scientific advancement.
Think what's possible.
A global healthcare leader, Novartis
has one of the most exciting product pipelines in the industry
today. A pipeline of innovative medicines brought to life by
diverse, talented, performance driven people. All of which makes us
the most rewarding employer in our field.
Quality Manager America's
Job ID64316BRDivisionConsumer HealthBusiness UnitCIBA VisionCountryUSAWork LocationUnited States - GeorgiaCompany/Legal EntityUSA CIBA Vision Corporation Duluth GAPosting Functional AreaRegulatory/QualityJob TypeFull TimeEmployment TypePermanentJob DescriptionA global eye care leader, CIBA VISION has one of the most exciting product pipelines in the industry today. A pipeline of innovative contact lenses and lens care products brought to life by diverse, talented, performance driven people who share a passion for healthy vision and better life. All of which makes us one of the most rewarding employers in our field. How do you spend your day? Are you passionate about what you do? At CIBA VISION, our focus is clear, our purpose defined. We are part of a team that is making a difference in the quality of people's lives. Think what's possible. The Americas Quality Manager is responsible for the implementation and enhancement of all elements of the Quality Management System (QMS) in AMERICAS including the Novartis Quality Manual implementation. This position reports into the Duluth, Georgia, location, but incumbents can be located in Latin America or North America. Duties include: -Develop and improve the Quality Management System (QMS) in the AMERICAS region-CV liaison for ANVISA (Brazilian Health Regulatory Agency)-Align the Global Quality strategy with the Business Strategy at AMERICAS-Implement Novartis Quality Manual-Monitor internal compliance in AMERICAS including the CAPA (Corrective and Preventative Action)-Monitor and audit key suppliers-Americas-Mentor and support compliance activities (e.g. complaints, NCR?s, field assessments)-Conduct training for quality compliance and supplier management requirements-Leverage and synergize with Novartis resources in AMERICASMinimum requirementsMinimum Education Required: BS Degree in Engineering or Scientific fieldPreferred Education Level: BS in scientific disciplineMinimum Experience Required: 3-6 years experience in FDA Regulated Industry (Devices or Drugs) with experience in 3rd party management and external quality auditing. Familiar with ISO and FDA requirements.Preferred Experience Level: 7+ years practical experience in FDA regulated industry with solid experience of medical device requirements and supplier quality auditing with 3rd party management in a large multinational medical device or Pharma company.Minimum: Fluent in English and Spanish, computer literacy with standard software platforms, good verbal and written skills, ASQ Certification as Quality Engineer, Quality Manager, Quality Auditor.Preferred: same as above along with supervisor experience, ability to travel to South American countries. As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules. CIBA VISION is an equal opportunity employer M/F/D/V.
To learn about other Novartis opportunities, click here.
Job Title: Director of Quality Management
Company: Georgia Department of Behavioral Health and Developmental Disabilities
Location: Atlanta, GA
Description:
director, quality management, compliance, operations
The Georgia Department of Behavioral Health and Developmental Disabilities , (DBHDD), is seeking qualified candidates for the position of Director of Quality Management in the Office of Accountability and Compliance to oversee the system-wide management program for hospital operations in the CRIPA (Civil Rights of Institutionalized Persons Act) Settlement Agreement with the Department of Justice. Under broad supervision, provides energetic and visionary leadership in the planning, development and implementation of a system-wide quality management program for hospital operations within the Department of Behavioral Health and Developmental Disabilities (DBHDD). Provides leadership and consultation for all hospital-based quality management directors. Assures that all hospital related quality management issues are systematically and systemically addressed, including requirements found in the Centers for Medicare and Medicaid (CMS) Conditions of Participation for Hospitals, The Joint Commission (TJC) and in the Civil Rights of Institutionalized Persons Act (CRIPA) Settlement Agreement with the Federal Department of Justice. Supervises the quality management data manager assigned to hospital operations within the Department of Behavioral Health and Developmental Disabilities.Please email your cover letter and resume in Microsoft Word format to: Register to View .
To ensure proper routing/handling of your credentials, copy/paste or type the following title in the subject line of your email: Director of Quality Management
Job Title: Bilingual (Korean/English) Quality Manager
Company: Randstad
Location: Lithia Springs, GA
Description:
We are seeking candidates for all levels within this start up company. Immediately we have positions available for Bilingual (Korean/English) Quality Manager, Production Manager, and Plant Manager to oversee and drive productivity in a manufacturing environment. Plans, coordinates, and directs quality control program designed to ensure continuousproduction of products consistent with established standards: Develops and analyzesstatistical data and product specifications to determine present standards and establishproposed quality and reliability expectancy of finished product. Formulates and maintainsquality control objectives and coordinates objectives with production procedures incooperation with other managers to maximize product reliability and minimize costs. Helpdevelop with Production Manager the following:1. QA/QC certification and inspection reports documentation.2. Production and QA/QC manual documentation.3. ISO 9001 certification and other documentation.4. Executing actual product QA/QC tests.5. Communication with production team and monitoring production activities.6. Understanding products and managing overall production procedures.Working hours: flexibleMinimum requirements1. Entry level experience.2. Must speak both Korean and English fluently.3. Metal engineering or mechanical engineering preferred.4. Must be proficient in Microsoft Office (Excel, Word, Powerpoint).5. License in gas industry (hazmat certification)Please apply directly to the job posting or in person with resume on Monday between 10am-3pm.Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.
Job Title: Director of Quality Management #1040460
Company: Georgia Department of Behavioral Health and Developmental Disabilities
Location: Atlanta, GA
Description:
Oversee the system-wide management program for hospital operations in the CRIPA (Civil Rights of Institutionalized Persons Act) Settlement Agreement with the Department of Justice. Under broad supervision, provides energetic and visionary leadership in the planning, development and implementation of a system-wide quality management program for hospital operations within the Department of Behavioral Health and Developmental Disabilities (DBHDD).Provides leadership and consultation for all hospital-based quality management directors. Assures that all hospital related quality management issues are systematically and systemically addressed, including requirements found in the Centers for Medicare and Medicaid (CMS) Conditions of Participation for Hospitals, The Joint Commission (TJC) and in the Civil Rights of Institutionalized Persons Act (CRIPA) Settlement Agreement with the Federal Department of Justice.Supervises the quality management data manager assigned to hospital operations within the Department of Behavioral Health and Developmental Disabilities.Georgia´s Department of Behavioral Health and Developmental Disabilities is an equal opportunity employer.
Job Title: Quality Supervisor
Company: Company Confidential
Location: McDonough, GA
Description:
QUALITY SUPERVISORManufacturing facility looking for a qualified supervisor to coordinate quality initiatives designed to ensure customer satisfaction and continuous production of products consistent with established standards. Reviews product specifications to ensure current standards and procedures meet requirements. Writes work instructions and product testing procedures. Performs audits of quality systems.Supervises Quality Control personnel on 24/7 shifts.AS Degree plus 2-5 years supervisory experience. Statistical analysis, SPC data skills and knowledge of metric system and basic measurement instruments are required. Strong interpersonal and team building skills are essential.Please send resume, with salary requirements, to Register to View .
Job Title: Director of Hospital Quality Management
Company: Georgia Department of Behavioral Health and DD
Location: Atlanta, GA
Description:
Employer Information About Georgia Department of Behavioral Health and DD The Georgia Department of Behavioral Health and Developmental Disabilities (DBHDD) job site. At DBHDD, our mission is to support the recovery and independence of people with MH, DD, and AD. We welcome any prospective employees who demonstrate the same commitment. DBHDD is Georgia’s newest state agency, which began operating on July 1, 2009. Being a new organization provides DBHDD both challenges and opportunities that are unique and rewarding, including expanding Georgian’s understanding of a....more info View all our jobs Job The Georgia Department of Behavioral Health and Developmental Disabilities, (DBHDD), is seeking qualified candidates for the position of Director of Hospital Quality Management in Office of Accountability and Compliance to oversee the system-wide management program for hospital operations. Under broad supervision, provides energetic and visionary leadership in the planning, development and implementation of a system-wide quality management program for hospital operations within the Department of Behavioral Health and Developmental Disabilities (DBHDD). Provides leadership and consultation for all hospital-based quality management directors. Assures that all hospital related quality management issues are systematically and systemically addressed, including requirements found in the Centers for Medicare and Medicaid (CMS) Conditions of Participation for Hospitals, The Joint Commission (TJC) and in the Civil Rights of Institutionalized Persons Act (CRIPA) Settlement Agreement with the Federal Department of Justice. Supervises the quality management data manager assigned to hospital operations within the Department of Behavioral Health and Developmental Disabilities. NOTES: US Residents Only. Employer will assist with relocation costs
Description:
Supervises a small number of staff on a particular project or team by assigning and checking work. Coordinates the flow of work amongst staff members to ensure continuity and completion.Performs problem management and escalation to support staff and management using established policies and procedures.Maintains relationships with customers; analyzes customer concerns and issues and addresses issues appropriately and promptly.Assists in preparing and/or reviewing records and reports. Recommends changes to quality control standards to improve efficiency.Researches and evaluates operations technologies in order to help establish their potential use. Tests new and modified programs or work routines.Recommends and/or initiates the selection and hiring of employees. Trains and evaluates employees to enhance their performance, development, and work product. Addresses performance issues and makes recommendations for personnel actions. Makes recommendations for salary increases, transfers and terminations to manager.Develops, monitors and administers training programs for quality assurance and quality control.Serve as lead auditor in support of the internal audit program.Acts as a Subject Matter Expert (SME) for process development, process improvement and service improvement projects.Performs quality assurance monitoring for peer review and system integration testing.
Description:
A health care company with global reach. A product pipeline filled to the brim. A team committed to scientific advancement. Think what's possible. A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us the most rewarding employer in our field. Quality Manager America'sBusiness Unit:CIBA VisionDivision:Consumer HealthCompany/Legal Entity:USA CIBA Vision Corporation Duluth GAWork Location:United States - GeorgiaPosting Functional Area:Regulatory/QualityJob Type:Full TimeEmployment Type:PermanentJob Reference Code:64316BRJob Description:A global eye care leader, CIBA VISION has one of the most exciting product pipelines in the industry today. A pipeline of innovative contact lenses and lens care products brought to life by diverse, talented, performance driven people who share a passion for healthy vision and better life. All of which makes us one of the most rewarding employers in our field.How do you spend your day? Are you passionate about what you do? At CIBA VISION, our focus is clear, our purpose defined. We are part of a team that is making a difference in the quality of people's lives.Think what's possible.The Americas Quality Manager is responsible for the implementation and enhancement of all elements of the Quality Management System (QMS) in AMERICAS including the Novartis Quality Manual implementation. This position reports into the Duluth, Georgia, location, but incumbents can be located in Latin America or North America.Duties include:-Develop and improve the Quality Management System (QMS) in the AMERICAS region-CV liaison for ANVISA (Brazilian Health Regulatory Agency)-Align the Global Quality strategy with the Business Strategy at AMERICAS-Implement Novartis Quality Manual-Monitor internal compliance in AMERICAS including the CAPA (Corrective and Preventative Action)-Monitor and audit key suppliers-Americas-Mentor and support compliance activities (e.g. complaints, NCR?s, field assessments)-Conduct training for quality compliance and supplier management requirements-Leverage and synergize with Novartis resources in AMERICASMinimum Requirements:Minimum Education Required: BS Degree in Engineering or Scientific fieldPreferred Education Level: BS in scientific disciplineMinimum Experience Required: 3-6 years experience in FDA Regulated Industry (Devices or Drugs) with experience in 3rd party management and external quality auditing. Familiar with ISO and FDA requirements.Preferred Experience Level: 7+ years practical experience in FDA regulated industry with solid experience of medical device requirements and supplier quality auditing with 3rd party management in a large multinational medical device or Pharma company.Minimum: Fluent in English and Spanish, computer literacy with standard software platforms, good verbal and written skills, ASQ Certification as Quality Engineer, Quality Manager, Quality Auditor.Preferred: same as above along with supervisor experience, ability to travel to South American countries.As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.CIBA VISION is an equal opportunity employer M/F/D/V.To learn about other Novartis opportunities, Click here