QA Technician Jobs

Job Title: Quality Assurance Specialist Company: Sierra Nevada Corporation Location: Greenville, TX Description: The Quality Assurance Specialist is a member of the program team with emphasis on the quality requirements derived from the contract, specifications, drawings, and unique program requirements. The primary job of a program QS is to ensure the efficient implementation of the Quality processes as they pertain to programs. The primary job of a QS outside of direct program responsibilities is to efficiently collect metrics, analyze trends and evaluate processes for continual improvements. Additionally, the QA Specialist is responsible for resolving quality issues that impact program cost and schedule. Other responsibilities include assigning appropriate quality codes to Purchase Requisitions, interfacing with Government Quality Representatives concerning program quality issues, participating as a team member in resolving Corrective Action Requests, interfacing with vendors regarding quality issues, and maintaining data collection of quality related program data. The QA Specialist performs in-process inspections/audits and witnesses in-process and acceptance testing when required. The QA Specialist inputs to Cost Of Quality reports at the program level and conducts internal audits at the process/work instruction level to verify compliance to released processes and procedures. SNC job descriptions are meant as summarizations only. They do not necessarily reflect all duties and responsibilities of a position. ESSENTIAL FUNCTIONS: • Contract review for quality requirements. • Review of Manufacturing Work Instructions for appropriate inspection points. • Evaluate current processes, procedures, and instructions for efficiency and streamlining. • Conduct process audits of critical manufacturing process instructions/procedures. • Prepare inspection requirement cards for receiving inspection. • Review and assign quality codes to purchase requisitions. • Perform MRB and Corrective Action requirements. • Perform drawing and specification review as member of Configuration Control Board. • Coordinate with Government Quality Representatives on program quality issues including inspection schedules. • Coordinate with vendors on program quality issues. • Attend and participate in program meetings and reviews. • In-process and Acceptance test monitoring/surveillance. • Track FRACAS data and prepare FRACAS reports when required. • Assist in statistical data collection, analysis, and presentation to illustrate product quality trends. • Punctuality to work each day and prepared to work scheduled work hours. ADDITIONAL RESPONSIBILITIES: • Perform QA Inspector duties as required. EDUCATION/EXPERIENCE REQUIRED: • A.S. Degree in a electronic, mechanical, or industrial technical discipline preferred. • Experience with contract review for quality requirements. • Knowledge and utilization of ISO 9001 and applicable Military Standards and Specifications. • Minimum of five (3) years in an electronic/mechanical systems environment performing similar duties. SKILLS REQUIRED: • Excellent communication skills, both written & verbal. • Ability to work independently and make appropriate decisions. • Strong computer skills are required with good working knowledge of the MS Office Suite, including MS Project. • Ability to read and interpret drawings (electrical & mechanical), parts lists, specifications, instructions, and test procedures. • Strong math skills including basic trigonometry. • Understanding of Geometric Dimensioning and Tolerancing. • Ability to use advanced inspection tools. *SNC is an EEO employer committed to recruiting a diverse workforce. Apply online for immediate consideration at www.sncorp.com or send inquiries to Melanie.Campbell- Register to View

Job Title: QA Technician Company: ASK FOODS, INC> Location: Palmyra, PA Description: QA TECHNICIAN Tasks for this day or night shift position include: incoming inspection of ingredients, monitoring temperatures of production areas and products in a cold environment, sanitation inspections, weight checks, thermometer calibrations, and maintaining databases. Background in HACCP and some exp in a food processing environment are preferred. Chemistry or microbiological background is a plus. For consideration please fax Register to View ), email href=mailto: Register to View > Register to View , or mail your resume and salary requirements to HR Dept: ASK Foods Inc. P. O. Box 388, Palmyra, PA 17078.

Job Title: Localization QA Specialist - Android Smart Phone Company: Motorola Location: Sunnyvale, CA Description: Localization QA Specialist - Android Smart Phone Job Localization QA Specialist - Android Smart PhoneJob ID 88537LocationUNITED STATES - CA - SUNNYVALEJob Category Software Engineering , QualityPosition TypeExperiencedEducation RequiredUnknownExperience Required5 - 10Basic Qualifications- Bachelor's degree in localization or linguistics and/or a relevant field with a strong academic record. Master's degree a plus.Department Description We are at the intersection of all things cool in the valleyWe are a Sunnyvale, CA based software applications and services development team in the heart of Silicon Valley that is combining the best of the internet, messaging, and social networking into intuitive software, called MOTOBLUR. MOTOBLUR is an innovative cloud-assisted solution to manage and integrate messaging, social networking, and other web services and will debut on the T-Mobile/Motorola CLIQ with MOTOBLUR Android smartphone. This product aggregates contacts, posts, messages, photos and more from sources including Facebook, Twitter, MySpace, Gmail, and Microsoft Exchange and many more to come.In collaboration with Google's Android team, we are driving and developing a massively scalable ecosystem. Android is the first free, open source and fully customizable platform built for the mobile internet. Android offers a full stack: an operating system, middleware, and key mobile applications from Google and other. It also contains a rich set up API's that allows third party developers to develop great applications.We're financially strong and stable, in the last year generating $300M in positive cash flow; with over $7B in cash and short term investments.Be part of something innovative & cool which will reshape the mobile internet and be used by millions of people worldwide. Be part of the resurgent Motorola Mobile Devices business and create applications and services that will enhance the lives of everyone who uses them.Scope of Responsibilities/Expectations Develop and maintain generic localization style guide and ensure adherence by SW translation vendors in Europe and Latin America Develop English source glossary (and format) working with Design teams and Product Management teams in order to ensure consistent usage of product terminology Ensure English product source follows terminology guidelines Ensure localized products have excellent translation quality for the Latin American and European market by working with regional offices on translation process improvements and by monitoring/providing feedback on vendor deliveries on a weekly basis Interact with tech writers, designers, project managers, QA manager and linguists in order to prevent linguistic UI defects Test and monitor localization project progress and UI quality and report project status to management on a weekly basis Analyze localization defect types, and frequently provide metrics to management UI localization debugging on native language may be requiredSpecific Knowledge/Skills Bachelor's degree in localization or linguistics and/or a relevant field with a strong academic record. Master's degree a plus. At least 5 years experience working with Localization technologies, including Translation Memories, Translation Management Systems, Terminology Management, and Machine Translation. 3+ years experience localizing software, preferably for mobile devices. Solid knowledge of Linguistic QA processes and up-to-date knowledge of localization issues and trends is a must Solid knowledge of translation and authoring tools such as: Catalyst, Dejavu, Trados Exposure to mobile technology and terminology a must Bilingual (Western European or Latin American languages preferred), knowledge of a third language a plus Working knowledge of some of the major platforms such as Windows, Mac, Linux Be a team player with a positive attitude and quality orientation.APPLY DIRECTLY TO JOB #88537 at:http://www.motorolacareers.com/jobsearch_frames2.cfm?w=searchABSOLUTELY NO AGENCIES OR THIRD PARTY SOLICITATION!

Job Title: Statements Quality Assurance Specialist Company: J.P. Morgan Chase Location: Newark, DE Description: Wealth Management Operations supports JPMorgan WM, the worlds premier service provider for hi net worth individuals. The Private Banks goal is to help these affluent individuals across the globe optimize their wealth, after taxes and across generations. Located in Newark, Delaware, the 400 members of WM Operations provide end-to-end support for all aspects of the client banking experience, working closely with sales, service, and product specialty groups.JPMorgan Chase is a leading global financial services firm with assets of $1.1 trillion and operations in more than 50 countries. The firm is a leader in investment banking, financial services, transaction processing, asset and wealth management, and private equity. Under the JPMorgan and Chase brands, the firm serves millions of consumers and many of the most prominent corporate, institutional and government clients in the world.The Wealth Management (WM) Statement Operations team is responsible for statement rendering and quality assurance functions for WM Investment and Deposit statements. The Statement Rendering team is responsible for ad hoc client reporting, retrieving and mailing historical statements, special handling of mail, investigating statement mailing issues, and the tracking and remailing of returned mail. The team is also responsible for the electronic delivery of preliminary prospectuses for initial public offerings.The WM Statement Quality Assurance Specialist is responsible for the content of the Wealth Management Investment statement. This statement is generated from the Omni accounting platform and is the primary source of client reporting in PB and PWM. The specialist will have a firm understanding of securities operations, and be able to translate accounting postings to client reporting on the statement. The specialist will partner with Front Office to identify and resolve issues and make statement corrections. Additionally, the role involves working with Operations and technology to ensure statement accuracy and resolve out of balance statements.Core Responsibilities· Assist with Omni coding for account corrections and out of balance conditions; ensure corrected statements are available for review· Act as the escalation point for client issues, which involves working with the Front Office to resolve questions, investigate issues and develop a satisfactory response to the clients concerns.· Participate in project initiatives including: establish business requirements, performing UAT and implementing changes within the team· Represent the Statements space as SME on any projects with impact to Statements· Review all out of balance statements and drive resolution. This requires determining the cause of the out of balance condition and making the necessary corrections to generate a client statement.· Work with Front Office partners to understand client feedback and issues as they relate to the statement, and guide them to the appropriate resolution.· Perform market value and cost reconciliations on client statements.· Perform quality assurance on end of month statements to ensure statements are accurate and no defects were created when statements were generated.Required Experience/Skills· Strong analysis and problem solving skills· Strong client focus· Highly motivated and ability to work independently· Excellent verbal and written communication· Ability to develop maintain relationships with business partners· Commitment to quality and control· Ability to think creatively and recommend/implement process improvements· Strong organizational skills to successfully manage multiple tasks at one time· Strong background in use of computer systems (PC and Mainframe)Education· A.S/ B.S. degree or equivalent work experiencePreferred Experience/Skills· Project management experience a plus· Knowledge of Private Bank products/Services· Knowledge of the accounting for financial instruments, including derivatives and multi-currency instruments· Knowledge of financial products with an understanding of the attributes of investment products, as well as related calculations

Job Title: Senior Quality Assurance Specialist - GLP/GCP Company: Cubist Pharmaceuticals Location: Lexington, MA Description: Position Summary: Collaborates with Nonclinical and Clinical Research personnel to ensure that research practices comply with SOPs, regulations, and guidelines. Provides GLP and GCP compliance and general QA support; acts as liaison between product development teams and QA. Plans, coordinates and conducts internal and external (domestic and international) GLP and GCP -related audits. Cubist GLP Contributing Scientist Report Audits Vendor Audist (CROs, Labs) Trial Master File (TMF) Audits System/Process Audits Investigator Site Audits Study Directed Audits Review nonclinical documents for adequacy and compliance, as required. Assists in the development and maintenance of quality management systems. Reviews SOPs to ensure compliance with applicable regulatory and corporate standards. Participates in the development and delivery of internal training programs. Assists management in the preparation for regulatory agency inspections. Supports the preparation, coordination, and management of regulatory agency inspections of Cubist. Supports 'for cause' audits, as necessary. Keeps up to date with current regulatory guidelines and regulations. Minimum Basic Qualifications : Bachelor s degree in a scientific discipline 5 years in a pharmaceutical quality assurance / compliance role At least 3 years experience in an GLP auditing role, with one year as a lead auditor Experience Required: Working knowledge of 21 CFR Part 58 Must be able to partner with a diverse group of staff/consultants with different strengths and skills Ability to prioritize work and handle multiple assignments, while maintaining quality Ability to identify and/or resolve quality issues/discrepancies with others in a proactive, diplomatic, flexible and constructive manner Ability to work independently and as part of a team, detail oriented Excellent communication skills and investigative techniques Desired Competencies and Qualifications: Working knowledge of Code of Federal Regulations (CFR) and ICH Guidelines governing clinical research and familiarity with current initiatives One plus years in a GCP auditing role Working knowledge of 21 CFR Part 11 and Computer System Validation (CSV) Experience in international compliance / auditing Experience in developing and writing SOPs Auditor certification (ASQ, SQA) Work Environment: This position will be based in the Lexington, MA office Physical Demands: The candidate must be willing to travel (up to 50% during peak workloads) To perform this job successfully, an individual must be able to perform each essential duty satisfactorily within the context of the representative work environment and physical demands described above. Likewise, qualifications listed are representative of the knowledge, skills, and abilities required to perform the position s essential functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Job Title: Quality Assurance Technician Company: Location: Rochester, NY Description: Applicants should have at least five years experience within a job shop environment. Must be able to accurately inspect components using precision measuring instuments, CMM and open plate as well as performing in-process and final inspections. Candidates must have strong math and be detailed oriented.

Job Title: Temp, Quality Assurance Associate III Company: Stryker Location: Hopkinton, MA Description: The Temp, Quality Assurance Associate III is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all Stryker Biotech products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Participates in the internal and vendor qualification programs and makes vendor assessment recommendations.• Reviews all manufacturing and support records to certify compliance with specifications and procedures. • Releases product based on Quality Assurance record review and approval by QA Manager. • Performs regular internal audits of Stryker Biotech Manufacturing facilities as a lead auditor.• Works closely with Manufacturing and Quality Control to resolve open issues resulting from record reviews, internal audits of the facility, and deviation issues.• Performs vendor audits as scheduled.• Reviews and assesses Deviations, including evaluation, tracking, follow-up, and reporting / trending.• Reviews and approves Validation / Technical Reports.• Reviews and assesses Corrective and Preventive Action Reports• Participates in Regulatory Inspections.• Other duties as assigned.

Job Title: Quality Assurance Lab Technician Company: Advantage Staffing Location: Tyler, TX Description: Job Summary:• Observes production process for quality issues to ensure top-level product quality. • Performs various lab duties such as analysis of raw and finished products in order to ensure quality, testing of and monitoring of product pH, Brix and microbiological testing.• Researches and develops new products and innovative ways to improve product quality.

Job Title: RN, Quality Assurance Specialist Company: Logistics Health Incorporated Location: La Crosse, WI Description: RN, Quality Assurance Specialist Department: Medical Operations Facility: La Crosse, WI - Headquarters Schedule: Full Time (40 hours or more per week) Shift: 2nd Hours: Monday - Friday 2:30 p.m. - 11:00 p.m. Job Details: Job Summary: Evaluate a variety of medical exams, assessments and information while utilizing the nursing process. Determine medical fitness, ability to be deployed and capability to perform required job functions in accordance with the applicable regulatory standards. Identify emergent behavioral health issues and initiate intervention when necessary. Qualifications: Must be a graduate of an accredited nursing program such as a Bachelor's of Science in Nursing (BSN) and/or Associate's Degree in Nursing (ADN) with 4 to 5 years of recent clinical experience required. Medical/surgical background preferred. Position requires the ability to interpret lab results. Experience interpreting EKG results preferred. Knowledge of CPT and ICD9 coding and phlebotomy desired. Candidates must be currently licensed or able to obtain RN licensure in the state of Wisconsin or a compact state. Possession of or the ability to achieve and maintain a current certification in Basic Cardiac Life Support (BCLS) required. Proficient computer skills including Microsoft Office programs and database experience required. Applicants must be able to understand regulatory standards and their application to various medical examinations and documents. Must possess excellent oral and written communication skills. Analytical thinking and team work skills are required. Ability to perform detailed work with a high degree of accuracy is also required. *Position requires the ability to work a modified/weekend schedule as needed. This position offers an attractive compensation package including a discretionary bonus program as well as comprehensive benefits including health, dental, vision, short and long-term disability, life insurance, Section 125, 401(k), childcare assistance, fitness program/reimbursement and much more! Numerous openings available! Extended Deadline: Applications will be accepted until 5:00 p.m. CST on Monday, February 22, 2010. Logistics Health Incorporated is an Equal Opportunity/Affirmative Action Employer.

Job Title: Quality Assurance Specialist Company: Becton Dickinson Location: Wilson, NC Description: The Quality Assurance Specialist as a member of the Quality Release group is responsible for performing detailed inspections of packaging components (primary and secondary) consisting of visual, mechanical and testing functions and is responsible for all associated paperwork and documentation .This position will also perform sampling of incoming raw materials for QC testing analysis. The Wilson quality system is compliant to 21CFR 210 211 and Becton Dickinson Corporate policies. This position will take direction and report to the Quality Release Leader.Main Responsibilities:- Member of the Quality Release group responsible for inspection of incoming components, finished product and batch documentation in compliance with 21CFR 210211, Becton Dickinson Corporate policies, and all other applicable quality / regulatory requirements- Performs detailed inspections of primary and secondary packaging materials and components using visual, mechanical, and instrumentation methodology- Perform detailed inspection of finished product samples using visual, mechanical, and instrumentation methodology- Perform sampling of incoming raw materials per inspection plan for QC testing- Generate all cGMP documentation associated with work activities- Enter data/results in SAP and/or SQL LIMS- Maintain work area and instrumentation in a clean, sanitary, orderly, operational and safe condition- Perform required standardization on measuring equipment- Assist in maintaining standard operating procedures- Performs other related Quality duties as assignedThe Quality Assurance Specialist as a member of the Quality Release group is responsible for performing detailed inspections of packaging components (primary and secondary) consisting of visual, mechanical and testing functions and is responsible for all associated paperwork and documentation .This position will also perform sampling of incoming raw materials for QC testing analysis. The Wilson quality system is compliant to 21CFR 210 211 and Becton Dickinson Corporate policies. This position will take direction and report to the Quality Release Leader.Main Responsibilities:- Member of the Quality Release group responsible for inspection of incoming components, finished product and batch documentation in compliance with 21CFR 210211, Becton Dickinson Corporate policies, and all other applicable quality / regulatory requirements- Performs detailed inspections of primary and secondary packaging materials and components using visual, mechanical, and instrumentation methodology- Perform detailed inspection of finished product samples using visual, mechanical, and instrumentation methodology- Perform sampling of incoming raw materials per inspection plan for QC testing- Generate all cGMP documentation associated with work activities- Enter data/results in SAP and/or SQL LIMS- Maintain work area and instrumentation in a clean, sanitary, orderly, operational and safe condition- Perform required standardization on measuring equipment- Assist in maintaining standard operating procedures- Performs other related Quality duties as assignedRequired Skills and Knowledge - Bachelors degree in a scientific discipline and 3 years of relevant Quality Assurance or an associates degree with 10 years experience in a pharmaceutical manufacturing company. Experience with visual inspection techniques, statistical sampling (ANSI Z1.4 Sampling Plan), ability to recognize defects in materials inspected, ability to work in a fast paced environment, ability to handle a high volume of work and rapidly adapt to changing environment. Prefer an associate trained in six sigma methodology.Technical Area of Expertise - Good verbal and written communication, organization, prioritization, displays sound judgment, interpersonal and computer competency to perform job. Experience performing investigations and displays good problem-solving skills