QA Technician Jobs in Maryland

Job Title: MATERIAL COORDINATOR & QUALITY ASSURANCE SPECIALIST Company: Location: Frederick, MD Description: GLOBAL Defense Technology & Systems is now hiring! http://www.gtec-inc.com Register to View -inc.com

Job Title: Quality Assurance Specialist III 169494 (NCI) Company: SAIC Location: Frederick, MD Description: Quality Assurance Specialist III 169494 (NCI) Full Time    Regular posted 3/15/2010   Job Category CTR - Clinical/Regulatory Req ID 169494 Able to obtain security clearance? None Currently possess security clearance? None Location Frederick, MD   % Travel Relocation No Requirements The Vaccine Clinical Materials Program, SAIC-Frederick, Inc. supports the Vaccine Research Center in manufacturing materials for Phase I & Phase II clinical trials. This position is responsible for supporting QA management in the establishment and implementation of quality systems in accordance with cGMP. Performs internal and external audits and inspections to assure compliance with established quality systems and cGMP. Performs routine review of all documentation generated both internally and under contract in support of cGMP manufacturing, including but not limited to process batch records, environmental monitoring results, QC test results, process development data reviews, stability data, and validation packages. Participates in the generation and review of new and revised documents (SOPs, MPR, test records, critical support documents). Participates in trending key indicators (deviations, investigations, environmental monitoring excursions, CAPA). REQUIRED SKILLS: Bachelors degree from an accredited college/university in a scientific discipline or 4 years experience in lieu of degree. Foreign educated candidates who have completed part or all of their education outside of the United States must have their foreign education evaluated by an SAIC-approved accrediting organization to assure that it has met the equivalency of the qualifications of degree work in the United States. In addition to the education requirement, a minimum of 5 years related experience in a cGMP environment is required. Must understand quality systems compliant with FDA regulations for cGMP and have experience in the review of process batch records, and in performing routine audits. Must have the ability to clearly summarize and communicate compliance issues to staff. Working knowledge of Microsoft Office. This position is subject to obtaining a Public Trust Clearance. DESIRED SKILLS: Combination of QA and QC experience, working experience with cGMP.

Job Title: QA Specialist II/III Company: Human Genome Sciences, Inc. Location: Rockville, MD Description: QA Specialist II/III Location Rockville, MD Job ID   2731    Employment Status Full-Time Regular Required Experience 2-5 years Required Education Bachelors Degree or Equivalent Required Travel No Relocation Available No Summary/Description Human Genome Sciences (HGS) is a biopharmaceutical company with approximately 800 employees and world-class R&D and manufacturing facilities based in Rockville, MD. We have three promising products in late-stage development – one, raxibacumab, already commercialized with sales to the U.S, Government and two moving toward commercialization. BENLYSTA™ (formerly LymphoStat-B®) has successfully met its primary endpoint in the first of two Phase 3 trials in systemic lupus, and we expect to have results of the second BENLYSTA Phase 3 trial in November 2009. ZALBIN™ (formerly Albuferon®) has completed Phase 3 development in chronic hepatitis C, and we expect the submission of global marketing applications in fall 2009. We are developing both of these products in collaboration with world leaders in the pharmaceutical industry. Further, in July 2009, we secured a new purchase order for 45,000 doses of raxibacumab, a drug to combat inhalational anthrax, to be delivered to the U.S. Strategic National Stockpile over a three-year period. At HGS, people are the key to our success. We share a passion for scientific and business innovation, creating unique opportunities to contribute to the commercialization phase of our products. At HGS, you will have opportunities to learn and grow; interacting with talent of the highest caliber, and you will be supported by a culture committed to employee and leadership development. We offer a competitive salary and benefits package. HGS is an Equal Opportunity Employer EOE/AA M/F/D/V Please visit for further information on our company and to apply on-line for this position. Review complex GMP records and data; Partcipate in  internal and external audits; Lead investigations; Write and review GMP documents; Conduct GMP training; Participate in project teams; Track QA documents; Update data and develop searches and reports in databases Review executed batch records; Review COAs; Review supporting batch record documentation, as needed; Review deviations and CARs; Review critical systems data; Initiate product disposition forms; Perform in-process assessments; Review master batch records and SOPs; Assist with system and vendor audits; Present training; Perform change over walk throughs Requirements 2-5 years in a GMP environment Thorough understanding of GMP regulations; Ability to organize multiple priorities; Strong oral and written communication skills including group presentations; Strong interpersonal skills; Ability to function in a cross-functional team environment; Attention to detail; Ability to interpret complex data and draw conclusions; Ability to perform with minimal supervision; PC literate

Job Title: Senior Quality Assurance Specialist Company: Location: Baltimore, MD Description: Job Description: Eyemaginations, Inc. is a fast growing and dynamic Baltimore-based health care media company focused on solutions that support medical professionals, patients and corporations in communicating and understanding complex topics. Our in-depth experience with animation, design and software has enabled Eyemaginations to create integrated systems that provide clear and concise education solutions. If you are looking for a new challenge with a company with unlimited potential that values the creative process, then Eyemaginations may be the opportunity you are looking for. As Quality Assurance Manager, you will manage and lead several QA initiatives covering multiple software products. You will work collaboratively with the software development, product management, technical support, and creative departments, to help ensure the success of all products. Key Responsibilities: ? Draft and maintain test plans with the goal of ensuring applications meet business requirements, interface specifications, and system compliance needs. ? Manage and respond to software quality assurance issues in collaboration with technical support and development teams. ? Evaluate, plan, design, develop, and deploy testing techniques for new applications and enhancements to existing applications. ? Create and execute test scripts, cases, and scenarios. ? Conduct all types of application testing as needed, such as system, unit, regression, load, and acceptance testing methods. ? Analyze test results in order to discover and resolve bugs. ? Produce reports and documentation for all testing efforts and results. ? Communicate test progress, test results, and other relevant information to project stakeholders. ? Cultivate and disseminate knowledge of application-testing best practices. Competency and Skills: ? Strong knowledge of system testing and software quality assurance best practices and methodologies. ? Working knowledge of PC operating systems. ? Excellent planning and organization skills. ? Excellent verbal and written communication skills. ? High attention to detail and deadlines, with a focus on process management and coordination. ? High level of ethics, sense of project ownership, and dependability. ? Ability to thrive in fast paced environment and to learn quickly and adapt. ? Ability to multitask and shift priorities quickly. ? Experience working in a team-oriented, collaborative environment. Required Education and Qualifications: ? 3-5 years QA experience or equivalent combination of education and experience

Job Title: QUALITY ASSURANCE SPECIALIST Company: CELESTE CONTRACT PACKAGING Location: Easton, MD Description: Celeste Contract Packaging a growing contact manufacturer and packager of medical devices and OTC and prescription pharmaceuticals have an immediate need for a Full-time Quality Assurance Specialist. This individual will be responsible to perform/assist with cGMP process validations, lead all internal audits, assist with outside inspections, and provide training. He/she will also provide assistance in the development, implementation, evaluation and maintenance of the Quality program; review the validity of NCR's; assist with CAPA's, deviations, change control, complaints and OOS. This individual must have knowledge of process validation activities, be able to interface/communicate at all levels in/outside the organization, and have a minimum of ten years experience working in a FDA/GMP manufacturing environment. Bachelor's degree in Chemistry or related scientific discipline is preferred and must be highly motivated, self-starter, and a team player with the ability to plan and organize various tasks simultaneously.Celeste Contract Packaging offers a competitive salary and a comprehensive benefits package. Interested applicants should submit resume to: Celeste Contract Packaging, LLC Register to View P.O. Box 3382 7978 Industrial Park Road Easton, Maryland 21601 Fax: Register to View An EOE/AA employer M/F/D/V

Job Title: QA Associate Company: Pharmaceutics International, Inc. Location: Hunt Valley, MD Description: Description: A growing pharmaceutical company in Hunt Valley currently has the need for QA Associate. This position reports to the Director of QA. Job duties include, but are not limited to, perform AQL testing, submit samples for analytical testing, perform informal audits of the cGMP production area, complete cGMP documentation and perform annual product reviews. Must be able to write and review investigations and deviations/variances. Will assist with the implementation of quality systems. Requirements: 2-5 yrs. Experience in QA field Knowledge of cGMP regulations Ability to write GMP documents Ability to analyze data/information and resolve complex problems as required How To Apply: Applicants must have cGMP experience, good communication skills and a can-do, problem solving attitude. Pii offers a great benefit package including 401K. Corporate standards require drug testing and background investigations. Click Here To Print PDF Application Please mail or fax this PDF application. Attn: Meredith Wescott, HR Director Pharmaceutics International, Inc. 10819 Gilroy Road Hunt Valley, MD 21031 Fax: Register to View You may also submit this PDF application via email by using the apply button below. EOE Mission Statement To deliver a quality dosage form development service which meets all of our customers’ needs in a timely fashion.   See all jobs in Hunt Valley MD

Job Title: QA Specialist I--C1USA Company: Capital One Location: Bethesda, MD Description: Level: AssociateEvaluates contact center associate and customer interactions to determine level of adherence to company policies and procedures. Monitors associate behaviors against a list of standards specific to each business unit. Works with designated points of contact for business units to resolve issues that arise.Responsibilities:• Gather data regarding interactions between Internal and External Suppliers and Capital One customers by reviewing calls and cases of assigned Suppliers against specific established metrics (Regulatory Accuracy, Fulfillment Accuracy and Information Accurac• Facilitate the learning of non-exempt associates performing similar role and personnel at external suppliers through leading calibrations, writing reports, etc.• Creating new process monitors• Review work of non-exempt associates performing similar role.• Work with business points of contact for businesses being reviewed to resolve call capture issuesBasic Qualifications:• High School Diploma or GED • 1 Year experience in Financial services contact center• 1 Year experience in Communications and influencePreferred Qualifications:• Bachelors Degree in Quantitative field or Business Process Management • 2 Years experience in Financial services contact center• 2 Years experience in Communications and influence• 1 Year experience in Laws and regulations governing the company• 1 Year experience in Working with various analysis tools and methodologies Capital One will not file non-immigrant visa petitions for alien workers. As a recipient of TARP funding subject to the ARRA, Capital One will not sponsor new H-1B petitions or transfer existing H1B visas for new hires to Capital One.

Job Title: QA Specialist I - temporary Company: SeraCare Life Sciences, Inc. Location: Gaithersburg, MD Description: Position Summary:  This is a 12 week temporary position.  Primary responsibility is to provide support from a regulated systems perspective for a GXP/ISO manufacturing and services environment. This is a hands-on, tactical position which utilizes a high degree of sense of judgment, communication and accuracy of work. Activities include but are not limited to training, product label control, quality inspection, internal auditing, and release of raw materials, in-process and finished products and critical components. In addition, this position is responsible for maintaining the document control system and quality records including the review of batch records, raw materials and intermediate products and services.Qualifications:  Minimum 3 years in a Life Science, GMP/ISO manufacturing and 3 years experience working in a Quality Department. Excellent written, verbal, interpersonal and communication skills necessary. Ability to function in a minimally supervised environment with exception attention to detail required. To apply for this position, go to:  http://tbe.taleo.net/NA5/ats/careers/requisition.jsp?org=SERACARE&cws=1&rid=69 SeraCare Life Sciences, Inc. is an Equal Opportunity Employer, M/F/D/V

Job Title: Quality Assurance Specialist Job in FORT GEORGE G MEADE, MD Company: Federal Government Jobs Location: Fort George G Meade, MD Description: Job Description (Please follow all instructions carefully) Job Title: Quality Assurance Specialist Department: Department Of The Army Agency: Army Installation Management Command Job Announcement Number: NCBF10121768 Salary Range: 62,467.00 - 81,204.00 USD /year Series & Grade: GS-1910-11/11 Open Period: Wednesday, March 10, 2010 to Friday, March 19, 2010 Position Information: - This is a Permanent position. -- Full Time Duty Locations: 1 vacancy - MD - Anne Arundel County Who May Be Considered: Status CandidatesJob Summary:Challenge Yourself - Be an Army Civilian - Go Army! Civilian employees serve a vital role in supporting the Army mission. They provide the skills that are not readily available in the military, but crucial to support military operations. The Army integrates the talents and skills of its military and civilian members to form a Total Army.Organization(s): US Army Installation Management Command, US Army Garrison, Directorate of Logistics, Plans and Operations Division, Fort Meade, MDAbout the Position: NOTES: (1) If you are contacted regarding your claim of federal employment status, veteran's preference or education, you will be given 3 work days to provide any required documentation. VEOA/VRA eligibles must be able to provide a Member 4 copy DD214 and/or proof of Terminal Leave when contacted. (2) If, after reviewing your resume and or supporting documentation, a determination is made that you have inflated your qualifications and or experience your rating can and will be adjusted to more accurately reflect your abilities. Please follow all instructions carefully. Errors or omissions may affect your rating. (3) If selected, you must be able to report to work within 30 days.Who May Apply: Click here for more information. All current Federal employees serving on a career or career-conditional appointment in the competitive service. Reinstatement eligibles. Applicants eligible under Veterans Employment Opportunities Act of 1998 (VEOA) Veterans' Recruitment Authority (VRA). Interagency Career Transition Assistance Plan (ICTAP) eligibles. Key Requirements: U.S. Citizen Major Duties:Develops and implements Quality Assurance Surveillance Plans (QASP) for logistics services performed by contractors. Identifies specific services susceptible to evaluation through established quality assurance techniques and develops procedures for evaluating their acceptability. Coordinates with QAEs to assure surveillance activities are performed in accordance with the terms of contract and accepted quality assurance practices. Ensures that evaluation methods provide systematic and equitable review, including methods for determining acceptability or non-acceptability of performance. Ensures reports furnished by the contractor are submitted in accordance with the terms of the contract and evaluates reports to appraise the LPM of potential problems. Serves as the point of contact for the LPM, all customers, Contracting Officer, and QAEs on the day-to-day administration of the service support contracts. Qualifications:Click on link below to view qualification standard. General Schedule CONDITIONS OF EMPLOYMENT: (1) Must be able to obtain and maintain a Secret level security clearance. (2) Annual Financial Disclosure Statement/OGE/SF 450 required. SPECIALIZED EXPERIENCE: To qualify, you must have at least one FULL year specialized experience equal to the GS-09 grade level. Specialized experience is experience that equipped the applicant with the particular knowledge, skills and abilities required to perform successfully the duties of the position, and that is typically in or related to the position to be filled. Examples of specialized experience are: serving as a Contracting Officers Representative (COR) for logistics service contracts including the Laundry Contract and the Service Support Contract that provides for contractor performance of three (3) support functions including Transportation and Movements, Supply Services and Storage, and Maintenance. Please address the following Knowledges, Skills and Abilities within your resume. Failure to do so may result in an "ineligible" rating: (1) Knowledge of two or more logistics (combination of supply and/or transportation) programs and their relationship to the overall operation; (2) Knowledge of specialized methods and techniques, to analyze, report and evaluate the effectiveness and efficiency of the Directorate of Logistics Division program/operations; (3) Extensive experience in one or more areas of supply operations (above the using unit/activity level), transportation operations or logistic management programs; (4) Knowledge of interrelated processes which is used to develop and/or recommend new or revised local directives, policies and implementing instructions; and (5) Knowledge of technical specializations in order to provide authoritative interpretations and guidance to management officials and other personnel at the same, lower or higher levels within the organization and the Contracting Officer. The experience described in your resume will be evaluated and screened for the Office of Personnel Management's basic qualifications requirements, and the skills needed to perform the duties of this position as described in this vacancy announcement. Applicants who have held a General Schedule (GS) position within the last 52 weeks must meet the Time in Grade Restriction. Education can be substituted for experience. Review the qualification requirements for specific information. One year of experience in the same or similar work equivalent to at least the next lower grade or level requiring application of the knowledge, skills, and abilities of the position being filled. Must have 52 weeks of Federal service at the next lower grade (or equivalent). Only degrees from an accredited college or university recognized by the Department of Education are acceptable to meet positive education requirements or to substitute education for experience. For additional information, please go to the Office of Personnel Management (OPM) and U.S. Department of Education websites at - http://www.opm.gov/qualifications and http://www.ed.gov/admins/finaid/accred/index.html Foreign education must be evaluated for U.S. equivalency in order to be considered for this position. Please include this information in your resume. GS-11: One year of experience directly related to the occupation equivalent to at least the next lower grade level; or Ph.D. or equivalent doctoral degree or 3 full years of progressively higher level graduate education leading to such a degree or LL.M., if related; or equivalent combinations of experience and education. Other Requirements: Click here for more information. Must be able to obtain and maintain a Secret security clearance. Must file annual financial statement. Male applicants born after December 31, 1959 must complete a Pre-Employment Certification Statement for Selective Service Registration. Direct Deposit of Pay is Required. Failure to provide all of the required information as stated in the vacancy announcement may result in an ineligible rating or may affect the overall rating. One year trial/probationary period may be required.How You Will Be Evaluated:Resumes will be evaluated for basic qualifications requirements and for the skills needed to perform the duties of the position, as described in this vacancy announcement and identified by the Selecting Official for the position. Benefits:The Department of Defense offers excellent benefits programs some of which may include: Comprehensive health and life insurance Competitive salaries Generous retirement programs Paid holidays, sick leave, and vacation time Flexible work environment and alternate work schedules Paid employment related training and education Possible student loan repayment Payment of licenses, certification,

Job Title: Software QA Specialist Company: Apptis Location: Bethesda, MD Description: Apptis is looking for a Software QA Specialist to join our team in Bethesda, Maryland! The Software QA Specialist is responsible for developing and maintaining a System Test Plan for the project.  Apptis offers a competitive benefits package, which includes excellent medical and dental benefits, and a 401k plan with matching.  Conditions of employment:  All applicants receiving an offer of employment will be required to complete an Apptis application and sign a disclosure and authorization form for a background investigation.  All offers of employment are contingent upon satisfactory completion of the Apptis background investigation which may include a criminal check, education and employment verifications and for some positions a credit check.  In addition Apptis participates in the E-verify employment verification program. Apptis is an equal opportunity employer committed to support family values, integrity in the workplace, and an entrepreneurial atmosphere. U.S. Citizenship is required for most positions. An Equal Opportunity Employer. M/F/D/VAnalyzing, designing, implementing and executing test procedures based on documented system requirements, business rules, GUI design documents, UML design documents, etc. in accordance with the RUP and standard best practices for testing. Responsible for maintaining a RTM. Document, track, verify and report on defects. Test web-based or client server systems and writing/executing SQL queries. Testing database ingests. Deliver comprehensive and accurate test findings. Assign and verify completion of testing tasks. Proficiency with the Rational toolset, SQL queries, and object oriented datasets. Prefer experience with the SDLC and knowledge of CMMI best practices.Candidate should be able to document, track, verify and report on defects. Candidate should be comfortable testing web-based or client server systems and writing/executing SQL queries. Candidate should be comfortable testing database ingests. Candidate should be able to deliver comprehensive and accurate test findings. Candidate should be able to assign and verify completion of testing tasks. Candidate should be able to develop a LOE based on new requirements. Ability to work independently or in a team environmentMinimum of 2 years test experienceBachelors Degree requiredAbility to obtain and maintain a clearanceTest experience that equipped the candidate to successfully complete the test activities listed in the job descriptionExperience testing large databases and data transfer jobsExperience writing complex SQL queries If interested, please apply online at http://track.tmpservice.com/ApplyClick.aspx?id Register to View -2472