Quality Assistant Jobs

Job Title: Software Quality Assurance Assistant Company: Location: San Francisco, CA Description: Who is DAEGIS? We are a national company of 130+ employees, with offices in San Francisco, New York, Boston and Chicago. Daegis offers a complete suite of services to assist law firms, government entities and corporate counsel with the management of complex discovery projects. Our expertise includes data collection and preservation; FRCP consulting; database and project management; and advanced electronic discovery solutions. In addition, Daegis offers the comprehensive search and hosting platform, DocHunter. The tool allows for the rapid filter and accelerated online review of native electronic file populations for discovery and production purposes. We are looking to hire a Software Quality Assurance Assistant in our San Francisco office. Qualified candidates will have experience in black box testing of both web-based and Windows based applications; writing and maintaining test documentation such as test plans and test cases; ability to meet hard deadlines for testing and product delivery; and work in a collaborative environment. Responsibilities: - Hands-on black box testing of web based and Windows based applications. - Writing and maintaining test documentation such as test plans, scripts and cases. - Create and execute real-life test scenarios. - Proven ability to meet hard deadlines for testing and product delivery. - Advocate and effect product changes for overall quality improvements. Qualifications: - Experience: 1 or more years QA experience testing web-based and/or Windows based applications. - Understanding of QA methodologies and processes. - Self-motivated and proactive, ability to carry out test projects independently. - Technical aptitude and ability to learn new technologies quickly. - Significant experience working with the Windows OS, Internet Explorer, MS Office and MS SQL Server. - Detail oriented with strong analytical and time management skills. - Ability to move between projects as priorities shift. - Excellent verbal and written communications skills. - Knowledge of Team Foundation Server a plus. If you are interested in applying for this position AND have the above noted experience then please follow the instructions below, it is very important that you please read and follow these instructions thoroughly. 1. Your resume submission must contain job code # DEVQA03012010 2. Please include a cover letter with your salary expectations. 3. Should your resume be considered for an interview, please include a phone number and a preferred time of day for an initial phone interview. NO RECRUITING AGENCIES PLEASE.

Job Title: Quality Associate I - Company: ACT-1 Location: Thousand Oaks, CA Description: Job Description:Immediate need for a Quality Associate I to support domestic and international facilities in GLP/GMP activities for a section or department in the quality organization. Provide continuous improvement to the Group through Quality Systems. Conduct audits of GMP and GLP activities, documentation and reports for conformance to procedures, protocols and regulatory requirements.This section contains a list of five to eight primary responsibilities of this role that account for 5% or more of the work. The incumbent will perform other duties assigned.1) Review documentation for accuracy and compliance to procedures, and release or reject as appropriate. Obtain resolution on areas identified as non-conformance. Interpret and evaluate results in terms of acceptability to standards, procedures and regulatory requirements.2) Prepare and issue reports. Manage database including all QA personnel with the use of the Access program (trouble shooting, etc.) and modifications to the databases such as creating new reports, queries, forms, tables, etc.3) Coordinate Release Testing of product with the Analytical group.4) Initiate and obtain applicable approval for inventory and test requests..5) Proof read new or revised procedures for accuracy.6) Conduct analysis of written procedures and submit procedural changes as needed to meet Corporate, Divisional, and Regulatory Requirements.7). Participate in internal or external assessments, as required. Support process with timely closure of observations/audit items.8) Assist with audits of various reports (Protocols, Qualifications, Regulatory Submissions, etc.). Identify areas of non-conformance and inform managementTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.Strong interpersonal skills and great attention to detail are necessary. Must be a strong team player with good problem solving, and good verbal and written communication skills. Must be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations, Good Laboratory Practices and Good Manufacturing Practices.Include the education and experience that is necessary to perform the job satisfactorily.Associate degree in a scientific discipline and one to two years of experience in pharmaceutical industry or equivalent. Bachelor degree in the life sciences, business or other technical field preferred. You can view all of our jobs online at http://www.act-1.com/?sc=11&id=516426

Job Title: Quality Associate Needed for our Lakewood Plasma Donor Center (217204-052) Company: Grifols Location: Lakewood, CO Description: Under the supervision of the Quality Manager and Quality Supervisor perform Quality Assurance functions to ensure compliance with internal and external regulations and protocol. Perform daily donor record file review. Perform equipment quality control review ? daily, weekly, monthly, semi-annual and annual. Return equipment to service. Perform weekly review of equipment incident logs. Verification and release of sample shipment. Staging plasma shipment. Inspection of incoming supplies. Weekly employee observations.

Job Title: Transcription Editor & Quality Assurance Assistant Company: Location: Sarasota, FL Description: We are a leading international business transcription service in search of a person with impeccable English grammar and punctuation skills to help revise, implement and monitor our quality control initiatives. Most of our work consists of interviews, focus groups, lectures, meetings and executive notes. Our aim is to review all standards and develop formatting guidelines with an aim toward concsistency, accuracy and top quality. Qualifications: * Minimum 5 years relevent experience (copywriter, editor, transcriptionist, English teacher) * Master level command of English grammar and punctuation (this means you must be completely fluent with the proper use of and differences among an ellipse, colon, semi-colon, comma, hyphen, dash, double-dash and how to stop a run-on sentence). * Impeccable organizational skills * Mature and reliable * Team player * High speed internet access About us: We started our company in 2002 with $1600 and have rolled it in to a highly successful business since. In a time when the economy sees companies cutting jobs, we are growing rapidly. We are in an aggressive expansion mode, where we will be creating new service divisions in our offerings. Business is very good now and getting better. We are seeking a mature, responsible person whom we can count on. Our business allows us to work out of a home based office (or anywhere). The right person for this position will appreciate our relaxed, but dedicated work philosophy. Our methods are highly effective, sans the corporate bureaucracy that restrains so many businesses. We work extremely hard and need someone will a similar work ethic and commitment. The long term oppportunity can be substantial. We are looking for someone mature, responsible and reliable who can work with us as a significant team member. Most of this work can be done from home on a very flexible schedule.

Job Title: QUALITY ASSOCIATE I/CMM OPERATOR Company: LeadingEdge Personnel Location: Dallas, TX Description: We have 2 full-time positions for a supplier of automotive components. QUALITY ASSOCIATE I/CMM OPERATOR Requirement: Must Be Able To Pass Testing Job duties will include reading blue prints (mechanical parts drawings) and using mechanical and electronic gages. QUALITY ASSOCIATE II Requirement: Must Be Able To Pass Testing Job duties will include performing inspection functions in all areas (incoming, in process and final); knowledge and application of statistical process control and charts; the use of specialized gages such as CMM, optical comparator and air gages; the use of control plans; and the use and application of fundamental geometrical tolerances. To apply for either position, please forward your resume and call our office Register to View Must be able to pass a criminal background. Email resume to Register to View .

Job Title: QA Assistant Company: Roze Room Hospice Location: Los Angeles, CA Description: Roze Room Hospice has a position available for a Quality Assurance Assistant.  The position provides support for the Director of Quality Initiatives at the Los Angeles, San Fernando Valley and Ventura agencies.  Duties include assisting in chart reviews for pre-defined clinical criteria, assisting in data compilation and presentation development, and creation of meeting minutes for monthly and quarterly meetings.Must be detailed oriented and proficient in basis MS applications - Word, Excel, and Powerpoint.  Excellent verbal and written communication skills required with experience in writing meeting minutes.  Knowledge of medical terminology highly desirable.  LVN preferred.Must have reliable auto and insurance.

Job Title: Quality Assurance Assistant Manager Company: Location: Modesto, CA Description: Northern California food processing company is seeking an experienced Quality Assurance Assistant Manager with a minimum 5 years of experience in food safety and/ or quality in the food industry, including at least 1 year of supervisory experience. Food Science/Technology Degree is required as well HACCP training and SQF certification preferred. Bi-lingual Spanish is preferred. Relocation package negotiable. Salary to $70K DOE + benefits. Email resume to Register to View REQ#5246.

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

Job Title: QA assistant Company: Location: San Diego, CA Description: A qualified candidate must be familiar with ISO 13485:2003 and QSR; have hands on experience in document control, internal audit and external audit, CAPA, product release and non-conforming product handling, quality planning, organizing management review meeting, supplier qualification, data analysis. Prefer to have experience working in small IVD company, ideally IVD-reagent company. Interests or experience in regulatory affair is a plus. Other general requirements: · BS in Biology; · Lab work experience; · Excellent communication skills; · Excellent organization skills; · Must be able to multi-task · Excellent computer skills. · Detail oriented; · Must be a team player. · Must have project management skills

Job Title: Quality Associate Company: Leadingedge Personnel Location: Carrollton, TX Description: Quality Assocaite IIWe have a full-time position for a Quality Associate for a supplier of automotive components.Must be able to perform inspection functions in all areas (incoming, in process and final) knowledge and application of statistical process control & charts; the use of specialized gages such as CMM, optical comparator and air gages; the use of control plans; and the use and application of fundamental geometrical tolerances. Must be be able to pass testing. Must be able to pass a criminal background. Email resume to Register to View .