QA Director Jobs

Job Title: QA-DIR Company: Flight Line Products Location: Valencia , CA Description: Aircraft Interior manufacturing company has immediate opening for Quality Assurance Director. The ideal candidate must have minimum five years of supervisory experience in aerospace related company. Must be able to maintain and author FAA regulatory procedures. Good understanding and ability to maintain AS9100 quality system. Must be able to plan internal and vendor audit programs. Salary plus benefits, including medical, paid vacation and holidays.

Job Title: QA Manager Company: United Pharma LLC Location: Fullerton, CA Description: Quality Assurance Manager-Vitamin Manufacturer The Company United Pharma LLC is a soft gelatin vitamin and nutritional supplement manufacturing company located in Fullerton, California. Our company is dedicated to offering the highest quality nutritional products on the market today. Our management team has over 20 years of soft gel manufacturing experience, and our state of the art production area reflects our dedication to the quality of the products we manufacture. United Pharma LLC offers a unique environment that fosters individual growth and rewards performance. We offer competitive compensation packages, great benefits, and an enjoyable work atmosphere. We are currently looking for people who want to be a part of a fantastic company. Duties and Responsibilities: Review and approval of quality-related documents, including but not limited to: protocols; qualification, validation and stability reports; test results, including raw data; calibration certificates; temperature charts Tracking and trending of out-of-specification results, failure investigation, deviations, change controls (equipment and document), complaints, recalls or field alerts Approval and release of reviewed executed batch records, as appropriate Development of controlled documents and procedures pertinent to Quality Assurance (QA) activities and functions, as well as other procedures if deemed necessary Creation, issuance, tracking, review, approval and/or control of labeling materials Issuance, tracking, and control of laboratory notebooks and raw binders Monitoring and verification of qualification and validation processes to ensure compliance to written protocols, and regulatory requirements, as applicable Provide training, as needed, and keeps track of individual training needs, including follow-up with department heads or supervisors Provide QA guidance on verification activities Providing assistance to other personnel as requested with regards to any quality issues including document retrieval and archival Play active role during regulatory inspection, as needed Qualification and Experience: 2-3 years previous QA management experience Bachelor’s degree Excellent written and oral communication skills Knowledge of GMP and FDA regulations

Job Title: Quality Manager Company: Carlisle Interconnect Technologies Location: Tukwila, WA Description: SUMMARY: The Quality Manager is responsible for developing, documenting and establishing Quality system processes for compliance to the Aerospace AS 9100 requirements. Responsibilities include improving current procedures, implementing Quality processes and planning, developing, and leading continuous improvement throughout the company. The Quality Manager will also develop and implement process improvement initiatives in order to mature the quality system, including new and improved measurement systems to validate and analyze continual improvement initiatives. ESSENTIAL DUTIES AND RESPONSIBILITIES: Implement, improve and coordinate Quality Management Systems (QMS) processes throughout all Company locations. Establish, Implement, Evaluate & Maintain Quality reporting systems. Provide training in ISO/AS9100 requirements as required. Work with Manufacturing and Engineering in product problem solving as required. Work with Supplier Quality and Purchasing regarding supplier ratings and reporting. Manage an effective Corrective/Preventive action process. Manage an effective Internal Audit program. Provide support for Customer audits and requirements for quality system improvements. Responsible for maintaining and updating the quality management system (QMS). SUPERVISORY RESPONSIBLITIES: Document Control function and personnel Internal Auditors, including scheduling, training, and personnel Corrective and Preventative Action processes ADDITIONAL RESPONSIBILITIES: Work with other company locations to implement Part’s Manufacturing Approval (PMA) and/or Production Certificate (PC) FAA systems. Work with other company locations to assure ITAR compliance.

Job Title: Quality Engineer/Manager Company: Euro Pro Location: Newton, MA Description: Euro-Pro, a pioneer in innovative cleaning solutions and small household appliances, seeks a top talent Quality Program Manager/Engineer to join the team in Newton, MA. Founded over a century ago and recognized as a global leader and innovator in the industry, we continue to exceed expectations by providing today’s busy consumer with better and more efficient products that fit their lifestyle and make life easier. From cutting-edge chemical-free steam mops to state of the art kitchen appliances, Euro-Pro products are made and sold under the brand names of Euro-Pro, Shark, Ninja Infinity, and Bravetti. This position will be responsible for Quality and Reliability Engineering for a product category. Duties include: * Work with Engineering and Marketing to identify customer expectations for new products or product improvements * Work with Engineering to establish solid and testable specifications to ensure products meet market requirements * Work with Engineering during the design phase to ensure that products meet requirements * Conduct and coordinate testing activities in multiple locations * Work with engineering and manufacturing to drive continuous improvements of products To be qualified for this position you must have: * Bachelors’ in Engineering or equivalent field * 10 years experience in technical or project management role * 5 years experience in consumer appliances * 5 years experience in quality and/or reliability engineering * Experience conducting FMEA and detailed design review * Experience in design engineering and/or manufacturing preferred * Experience with Six Sigma or other quality programs preferred At Euro-Pro, we are driven to be the best in the industry. We are looking for individuals who want to make a difference. We celebrate and reward initiative, creativity, growth, and commitment to our mission. We will provide the challenge and the opportunity to apply all aspects of your experience and skills; you provide the energy, passion, and results. If you would like to explore a possible fit with our dynamic and growing company, please forward your cover letter, resume, and salary history to Register to View -pro.com. No phone calls please. Euro Pro is an EEO/AA employer Search words: consumer goods, consumer products, housewares, appliances, kitchenware, vacuum, hand vac, sweeper, toaster over, slow cooker, blender

Job Title: Operation Quality Manager East Company: Land O' Lakes, Inc. Location: Nashville, TN Description: Land O'Lakes, Inc. would be nothing without our amazing employees. All 9,000 of them. Today, we are a Fortune 250 company with more than $12 billion in annual revenue (2008) and the third-largest cooperative in America. This success reflects the efforts, commitment and pride of our employees. As we continue to build on this success, we’ll always be looking for talented people to help us grow. Since 1921, we have been member owned and operated. We are a market- and customer-driven cooperative committed to optimizing the value of our members’ dairy, crop and livestock production. We do business in all fifty states and have a presence in more than fifty countries, with our headquarters in St. Paul, Minnesota. Here at Land O’Lakes, Inc., we value and recognize the unique talents and potential of all employees, and we are dedicated to being a high-performing organization built on the foundation of a diverse and inclusive workforce. If you are interested in becoming a part of this amazing team, please visit our website at www.landolakes.jobs. Land O’Lakes Purina Feed LLC, a wholly-owned subsidiary of Land O’Lakes Inc, is North America’s leading feed company, providing producers, cooperatives and dealers with an extensive line of animal feed, ingredients and services. We are currently seeking: Operations Quality Manager - East Region [5874BR] Field Based Position Purpose: As an Operations Quality Manager for our animal feed division, your primary role is to be a liaison between corporate and regional plant level Quality Assurance. Your goal is to insure compliance with quality, regulatory and feed safety systems in order to protect our customers and ultimately our brands. You will provide support, leadership and representation to assigned plants and teams for quality related training and guidance. The position will be heavily focused on working with facilities to develop and implement preventative quality systems and solutions in a multi-plant environment, while insuring continuous regulatory compliance. This position is Home Based on the East Coast, various locations possible, and requires 50 - 70% travel. Required (Basic) Education/Experience: To be considered, you must have a BS in Ag/Food/Dairy Science or related field AND 5+ years of progressive quality assurance experience in feed/food or related operations. You must have a thorough knowledge of regulatory requirements (FDA, State), product safety, GMP and preventative quality systems. Must have knowledge of trace/recall, critical process measurement, hazard analysis, product design/specifications and systems approach. Required Competencies and Other Skills: Strong communication and interpersonal skills and the ability to teach, coach and implement Quality Programs are essential. Must have a demonstrated ability to lead and drive change. Strong analytical problem solving/root cause analysis skills are essential. Must be able to effectively communicate at the plant and corporate level via oral and written reports. Preferred Education/Experience: Previous feed/food or related operations experience Preferred Competencies and Other Skills: Proficient with the concepts of HACCP, risk assessments, and application/implementation Travel: 50% or more Land O' Lakes, Inc. offers a competitive compensation and benefits package, including medical and dental insurance, retirement savings account, tuition reimbursement, PTO, paid holidays and employee development opportunities. Land O’Lakes, Inc. is an Equal Employment Opportunity and Affirmative Action Employer. Land O’Lakes, Inc. enforces a policy of maintaining a drug-free workforce, including pre-employment substance abuse testing. Additional information about our organization can also be obtained at www.landolakesinc.com.

Job Title: Quality Assurance Manager Company: Accellent Inc. Location: Upland, CA Description:     Currently, we are searching for a  to join our  facility. About the Opportunity: POSITION SCOPE / SUMMARY   The company provides design and outsourced manufacturing, assembly, and supply chain management to the medical device industry. With approximately 20 locations, Accellent employs 3000 people in 5 countries. Quality oversees the development of quality systems, standards and protocols for quality assurance testing models. Quality assists in the design and implementation of policies and procedures for quality systems, product and process controls, testing and evaluating the precision and accuracy of products and/or equipment. The Quality Manager will be expected to provide leadership and management for QA activity in a manufacturing facility; interact with customers and provide leadership support for Engineering, Quality Systems and Process engineering.    KEY RESPONSIBILITIES   1.            Serves as management representative. 2.            Work collaboratively with Engineering, Operations, and other functional groups to successfully and seamlessly deliver to customers an integrated set of services and products. 3.            Work collaboratively with site management team to successfully and seamlessly deliver to customers an integrated set of services and products. 4.            Be a resource and mentor to other members of the management team, with a responsibility to develop people and support corporate goals of employee engagement. 5.            Talent acquisition and development. Recommends and executes personnel actions including promotions, performance reviews and any disciplinary measures.  6.            Responsible for business improvement programs and initiatives such as Complaint reduction, Quality System improvements (CAPA, NCR, Training, etc), cost improvement programs through Lean Manufacturing techniques and drive successful business excellence programs for manufacturing to support business opportunities. 7.            Ensures output, timeliness, quality and Cost to standards consistent with customer requirements and company strategy. 8.            Support strategies to help drive improvements in operational capability required to support corporate growth and strategies. 9.            Reduce manufacturing operations costs through innovation and productivity gains. 10.        Create a continuous improvement culture that strives to satisfy customer requirements for fill-rates and zero defects. 11.        Complies with all work rules including those pertaining to safety, health, quality and Accellent Quality Management System. 12.        Develop and drive implementation of the quality system architecture, staffing, and associated processes to ensure adequate checks and balances exist as well as establishing the appropriate independence of the quality function.  13.        Leads management reviews, to ensure the quality system is suitable and effective to satisfy regulatory requirements and the company's quality policy and objectives and other applicable procedures and practices at all levels of the organization.   14.        Develops and drives a work culture fostering a highly ethical environment grounded in credibility and trust and fully committed to patient safety, compliance, quality and customer focus. 15.        Builds a strong quality team through staffing, leadership and training serving as a role model that drives improved compliance practices. 16.        Performs other duties as necessary.   QUALIFICATIONS   1.            Bachelors degree in engineering or technical equivalent degree 2.            10 years experience in manufacturing, preferably medical devices, including at least three years leadership responsibilities with increasing responsibility in quality assurance and associated fields. 3.            Must be familiar and understand recognized regulatory standards such as ( where applicable) US – CFR 21 part  820 (FDA QSR, GMP) ISO 13485 - (EN) ISO 13485 Medical Device Directive (MDD) 93/42/EEC Active Implantable Medical Device Directive (AIMD) 90/385/EEC In Vitro Diagnostic Medical Device Directive (IVDD) 98/79/EC ISO 13485 under Canadian Medical Device Conformity Assessment System (CMDCAS) ISO 14971 AS9100 ISO 9001 4.            Able to be technically comprehensive and knowledgeable including standard business ERP system principles, as well as technical aspects such as statistics, documentation, SPC, Geometric Tolerencing and mechanical drawings and associated software packages.  5.            Familiar with Six Sigma and/or a history of lean manufacturing, Kaizen and 5S, etc. Six-Sigma certified or willing to obtain certification preferred. 6.            Must possess excellent verbal & written communication skills, as well as presentation, organizational and management skills. 7.            History of recruiting and retaining exceptional talent. Due to the expected number of responses, only those most qualified will be contacted.  No recruiters please; all unsolicited third-party submissions will be rejected.     Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability.  To learn more about Accellent and our career opportunities, please visit us at www.accellent.com

Job Title: Quality Assurance Manager Company: The Henry M. Jackson Foundation Location: Rockville, MD Description: Responsibilities The Henry M. Jackson Foundation (HJF) is seeking a Quality Assurance Manager for the Department of HIV Laboratory Diagnostics and Monitoring in Rockville, Maryland. HJF provides scientific, technical and programmatic support services to the Department of Laboratory Diagnostics and Monitoring. The Military HIV Research Program (MHRP) is dedicated to HIV vaccine development, prevention, disease surveillance and care and treatment for HIV. HIV-1 continues to pose a significant and persistent threat to the military and allied forces both in terms of readiness and force protection. The brisk pace of deployments to locations throughout the world requires the MHRP to develop products and capabilities with an international scope. This program builds on the strength of the U.S. military medical research community, and addresses specific HIV research requirements to meet its mission: prevention of HIV-1 disease in the active force and, by extension, the global community at risk of infection. Responsibilities: 1. Reviews and approves documents. Develops and maintains a centralized documentation system for all records. 2. Ensure internal audits are performed each month and report findings at the monthly QA meeting after passing to the Lab Manager for review. Identifies critical episodes, events deficiencies, recommends remedial actions, confirms implementation of actions and reports findings to laboratory management. 3. Track the receiving of Proficiency test panels and submitting of results to vendor (generate a calendar of all PTPs to be received each year, documenting date received, date results submitted, and score received). The program includes serology/immunology, Western Blot, HTV-1 RNA Viral Load, HIV Genotype, Hematology and Flow Cytometry. 4. Coordinates all equipment/building validation issues and ensures regulatory compliance. 5. Reviews and tracks all Standard Operating Procedures (SOPs), medical device reports and Occurance Reports. Manages monitoring, evaluation, and corrective actions and reports the results to the appropriate department level committee. 6. Oversees the duties of 3 staff members: Document Control; QA Specialist and Technical Writer 7. Serves as the advisor and senior consultant to laboratory management and other officials on various aspects of laboratory performance improvement. Performs duties related to medical technology such as instructing and credentialing supervisors in the theoretical and practical aspects or the performance improvement program. 8. Manages external proficiency program to ensure that all analyses and procedures surveyed are in accordance with current accrediting and regulatory agency guidelines. Coordinates the ordering of surveys through the College of American Pathology (CAP), Accutest, and VQA. Manages the evaluations of surveys, requesting the investigation of all failed challenges and directing documentation of corrective action. 9. Represents HDRL on department level performance improvement and infectious control committees. 10. Manages the risk management program maintaining all incident report documentations and coordinating response to the appropriate committee. 11. Write SOPs as related to the Quality Management Plan 12. Completes other projects as needed. Required Knowledge, Skills, and Abilities: Mastery of medical technology principles, theories, practices, and methodologies to perform the full range of duties connected with the design and implementation of a clinical QC program. Comprehensive and detailed knowledge of accrediting and regulatory agency requirements, including federal and state laws. Knowledge of document control, validation/calibration of system and equipment and audit of records; excellent organization, computer and communication skills; ability to handle multiple priorities. Minimum Education/Training Requirements: Bachelor's degree in Science, Minimum Experience: 4 to 6 years experience in quality assurance Supervisory Responsibilities/Controls: Supervises Quality Assurance Technicians Work Environment: Office and laboratory environment Any qualifications to be considered as equivalents, in lieu of stated minimums, require the prior approval of the Director of Human Resources

Job Title: Quality Assurance Manager (Assistant Manager) Company: Location: Providence, ri 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: 1880939

Job Title: Quality Assurance Manager (Assistant Manager) Company: Location: Buffalo, ny 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: 1795219

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