20 Quality Assurance Testing jobs

Web Application Penetration Tester Coppell, TX ref send resume if a fit Web Application Penetration Tester Position Summary: Web Application Penetration Tester is responsible for hacking the web applications and APIs ethically, discover the exploits, assign the risk rating using CVSS score and report the vulnerabilities. Principal Responsibilities: Understand the application architectural components, business purpose of the application and code at high level Understand the threat and vulnerabilities reported in Threat Modeling, Static Code Analysis & vulnerabilities reported through open source scans Perform Pentest on Web Applications, APIs & Mobile Applications using block-box testing tools, in-depth penetration tests (using shell scripts and manual testing techniques), DAST & SAST scans Perform secure code reviews and code weakness w.r.t configuration, authentication mechanism, user data or roles definitions that could be exploited Writing executive...

SAP tester Worksoft Certify Redmond, WA ari Contract               : 12+ Months Job Description: SAP Tester with Worksoft Certify experience. Test Automation experience Good SAP functional testing experience – O2C or FI/CO Very good communication/coordination skills Ability to work independently

GUIDEWIRE TESTER GLENDALE. AZ keyp > > DURATION : FULL TIME / CONTRACT > > Job Description : > > 1. Functional expert on Guidewire Policy and Billing > Centre. > > 2. Proficient on PnC Insurance business > > 3. Hands on Testing experience on Guidewire Suite. > > 4. Total more than 12 years of experience and more than 5 > years on Guidewire Testing. >

QUALITY ASSURANCE AUTOMATION PROGRAMMER/DEV ST. PAUL, MN keyp > > ST. PAUL, MN > > LONG TERM > > F2F MUST > > NEED ONLY LOCAL CANDIDATES > > C2C, W2 WORKABLE > > ANY VISA > > SAMPLE TASKS > > * Develop Automated Test Scripts; > * Execute Automated Test Scripts; > * Create and maintain Test Automation Strategy; > * Create and maintain Test Automation Plan; > * Create and maintain Test Cases; > * Create automation documentation; and > * Create Test Closure Document. > * Assist the Performance Engineer in determining business flows to > be scripted and utilized in Performance/Load testing. > * Document all defects in the defect tracking tool in an accurate > and timely manner. > * Escalate all challenges to the appropriate resource(s) in a timely > manner. > * Communicate effectively both verbally and written. > * Attend Defect Review meetings. > * Assist in managing the overall scope of the...

Manufacturing Quality Engineer REC10018204 | Updated: May 16, 2020 OPENINGS: 1 JOB TYPE: Full Time LOCATION: Bethel, Vermont, United States INDUSTRY: Pharmaceutical / Biotech SALARY: $75,000.00 - $85,000.00 / year CATEGORY: Engineering EDUCATION: Professional Degree EXPERIENCE: 5-7 years TRAVEL: Never RELOCATION ASSISTANCE: WORK ELIGIBILITY: Green Card, US Citizen FEES: 9% of Salary CANDIDATE GUARANTEE TERMS: 30 days PAYABLE TERMS: 90 days DATE UPDATED: May 16, 2020 DATE POSTED: Feb 11, 2020 JOB DESCRIPTION The Manufacturing Quality Engineer is responsible for ensuring the quality of all products, quality system documentation, manufacturing process quality, and customer problem resolution. Specific Responsibilities Participates in product design reviews and Engineering hand-off approval. Resolves internal product quality problems to reduce defects/scrap. Champions product customer complaint cause and submits corrective action plans in the 8D or customer format....

Medical Device Quality System Manager Cambridge, MA ref 02142 MUST HAVE: Bachelor's Degree in Science or a higher degree in a technical discipline. 10 years of experience in working with Quality Systems. Experience in the Medical Device Industry. Experience in managing document control under a Medical Device QMS Experience in eQMS development and management Strong working knowledge of FDA, ISO 13485 and MDSAP requirements Must possess strong oral and written communication skills NICE TO HAVE: ASQ certification as CMQ/OE. Experience with MasterControl. ADDITIONAL COMMENTS: The perfect candidate would a professional with Quality Systems Management experience from the medical device industry. Our client highly prefers someone with a strong ISO background. Pre screen questionnaire: 1. Please walk us through your experience in working with Quality Systems specifically in the medical device industry. 2. Please describe your working knowledge of ISO 13485 and...

Manager, Quality Assurance Mountain View, CA Skills: Biotechnology, GMP, GLP, Cellular products, Batch records, Quality Control, Quality Assurance send resume answers below if a fit 1.) Do you have a Bachelors Degree in biological sciences? If so, what is your degree in? 2.) Have you had a minimum of 5 years Quality Assurance experience in pharmaceutical or biologics? Describe 3.) List the industries for which you have worked in for Pharmaceutical, Biotech, or Medical Devices. 4.) Do you have manufacturing and/or production experience in Pharma, Biotech or Medical Devices? Describe what you have done and what you have been responsible to oversee. 5.) Describe your experience in working with cellular products. 6.) Describe your experience with QC certificates, closure of Batch Records, and deviation reports. 7.) Describe your experience with nonconformance disposition and release activities. 8.) Describe your experience working with suppliers and...

Chief Quality Control – Federal Construction Montgomery, Al THR Chief Quality Control – Federal Construction Montgomery, Alabama - Based on qualifications Negotiable Full-time Various Locations (Montgomery AL, Pittsburgh PA, and other locations based on potential new projects) Construction company looking for a Chief of Quality Control for Federal Construction. Must have a Construction Management degree and 10+ years of experience in a related role. Experience on Federal Construction projects and stable work history required.

Director of Quality, Risk & Perf Improvement Manassas, VA vs Job Description Our client, a 85+ bed hospital located in Northern VA, near Manassas, and 40 miles from Washington DC, has a need for a Director of Quality, Risk and Process Improvement to join their team. **This job requires a RN** The Director, Quality and Process Improvement is responsible for oversight of all quality initiatives to include monitoring quality metrics at the unit level. This position oversees regulatory readiness through assessment and implementation of measures to meet regulatory requirements. The Director, Quality and Process Improvement evaluates the overall care of patients by identifying opportunities for improvement in patient care practice. Through identification of process improvements and educational opportunities, communication, and reporting state of quality to several groups. 3 Direct Reports-Manager, Risk Management, Coordinator, Regulatory Accr, and Clinical Data Abstractor...

Tester  ETL tool  DB Kafka Unix/Linux  Franklin, Wisconsin gurpreet Location: Franklin, Wisconsin Type: Fulltime Experienced with Test Data and Test Environment Management skills Should monitor , maintain the test environments and systems Experienced with triaging the environment issues, install server certificates, server upgrades, code deployments from GIT Should have experience in creating and maintaining the test data across test environments. Should have experience in ETL tool (Informatica or similar) and DBs (MySQL, Sybase ) Knowledge on tools like Kafka and Unix/Linux systems

Quality Control cGMP Microbiology Supervisor Allendale, NJ ref About job Compensation: View Salary Referral reward:$4000Job type:Direct hireJob function:Quality ControlIndustry:BiotechnologyExperience level:Mid-seniorEducation level:Bachelor’s degreeJob classification:TechnicalLocation:Allendale, NJZip code:07401Skills:environmental monitoring within the biopharmaceutical industryExperience required:8 YearsRelocation assistance:No Local candidate preferredVisa requirement:Only US citizens and Greencard holders,EAD cardsNumber of positions:1 Pre screen questionnaire: 1. In which industries have you been responsible for Environmental monitoring in controlled environments? 2. Please list name of the Life Sciences or Biotechnology companies you have worked for. 3. Tell us types of laboratory testing you typically perform e.g. Plate reads and incubations, Growth Promotion, Microbial Identifications 4. What are your compensation expectations? 5. In peak...

Quality Control Microbiology Supervisor Allendale, NJ ref About job Referral reward:$250Job type:Direct hireJob function:Quality ControlIndustry:BiotechnologyExperience level:Mid-seniorEducation level:Bachelor’s degreeJob classification:TechnicalLocation:Allendale, NJZip code:07401Skills:environmental monitoring within the biopharmaceutical industryExperience required:8 YearsRelocation assistance:No Local candidate preferredVisa requirement:Only US citizens and Greencard holders,EAD card Direct hire Skills : Environmental monitoring within the biopharmaceutical industry. Quality Control Microbiology Supervisor The QC Microbiology Supervisor organizes, and directs staff to meet and exceed cGMP requirements, establish KPI’s, while adhering to quality control-microbiological and technical standards. Provides oversight of day to day activities including adjustment of workflow, test performance, and quality compliance. Essential Functions and...

QC Microbiology Analyst II & III (Environmental Monitoring) Allendale, NJ Skills : CGMP experience, Biotechnology Certificate, Environmental Monitoring, Clean Room. About job Referral reward:$250Job type:Direct hireJob function:Quality ControlIndustry:BiotechnologyExperience level:AssociateEducation level:Bachelor’s degreeJob classification:TechnicalLocation:Allendale, NJZip code:07401Skills:cGMP experience, Biotechnology Certificate, Environmental Monitoring, Clean RoomExperience required:2 YearsRelocation assistance:No Local candidate preferredVisa requirement:Only US citizens and Greencard holders,EAD cardsclose QC Microbiology Analyst II & III (Environmental Monitoring) This position will report into the Supervisor of QC Microbiology. The Quality Control Microbiology Analyst (Environmental Monitoring) serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst will coordinate data for batch release, participate...

QC Microbiology Engineer III Allendale, NJ ref About job Referral reward:$250Job type:Direct hireJob function:ResearchIndustry:BiotechnologyExperience level:AssociateEducation level:Bachelor’s degreeJob classification:ProfessionalsLocation:Allendale, NJZip code:07401Skills:Bachelors, Lab, analytical testing, GMP, SOP, Experimental dataExperience required:1 YearsRelocation assistance:NoVisa requirement:Only US citizens and Greencard holder Skills : Bachelors, Lab, analytical testing, GMP, SOP, Experimental data. QC Microbiology Engineer III This position will report into the Associate Manager of QC Microbiology. The Quality Control Microbiology Engineer III will support two sites in Allendale, NJ serving as a support role to clinical and/or commercial production. The QC Microbiology Engineer III will coordinate data for batch release, participate in project/client meetings, and author/revise microbiological testing procedures. Additionally, the QC Microbiology...

QA Compliance Investigator Allendale, NJ ref Direct hire Skills : Batch records review, Documentation management, CAPA, Non-conformance, Deviations, cGMP, FDA. About job Referral reward:$250 Job type:Direct hireJob function:Quality AssuranceIndustry:BiotechnologyExperience level:Mid-seniorEducation level:Bachelor’s degreeJob classification:TechnicalLocation:Allendale, NJZip code:07401Skills:Batch records review, Documentation management, CAPA, Non-conformance, Deviations, cGMP, FDAExperience required:5 YearsRelocation assistance:NoVisa requirement:Only US citizens and Greencard holders,EAD cards QA Compliance Investigator This position will report into the (Associate) Manager of Quality Assurance (Floor support). Responsible to perform Quality Assurance Compliance activities in support of company and/or client procedures, including but not limited to, document. management: investigations, CAPA, SOPs, qualification and validation reports, QC data. Supports...

Quality Assurance Spec :CAPA, cGMP/cGTP Process Compliance Allendale, NJ ref This position will report into the (Associate) Manager of Quality Compliance. Responsible to perform Quality Assurance Compliance activities in support of Quality Systems and/or client procedures, including but not limited to, document. management: investigations, CAPA, SOPs, qualification and validation reports, QC data. Supports Quality management with various department, organizational and operational excellence initiatives. Generally, exercises independent judgment, within generally defined practices and policies, when selecting methods and techniques for obtaining solutions. This role supports internal and external audits which may include interaction with Health Authorities and clients. Opening Investigation and closing out with CAPA. Essential Functions and Responsibilities Liaises with relevant functional groups (Operations, Facilitates, QC, EH&S) to provide guidance through all stages...

Quality Control Director (Pharmaceutical  manufacturing) Allendale nj rec Position Summary About job Only US citizens and Greencard holders This position will report into the Senior Director of Quality responsible for the oversight and management of Quality Control (analytical and microbiological) at the Clinical and Commercial sites in Allendale, NJ. Responsible for managing the laboratories daily activities and continuous improvement initiatives to ensure compliance and client requirements are met. Core responsibilities include, but not limited to, management of resources (human resources and financial resources), data integrity program and external laboratory management. Collaborates with other departments to support organizational and functional strategy. Represents Quality Control in internal and external audits which may include interaction with regulatory health authorities and clients.   Essential Functions and Responsibilities  ...

Quality Assurance Associate Level III Allendale, NJ Direct hire Skills : Batch records review, Documentation management, CAPA, Non-conformance, Deviations. Quality Assurance Associate Level III Responsible to perform Quality Assurance activities under direct supervision of daily tasks in support of Quality Systems and/or client procedures including but not limited to document management, review of QC data, material releases and final product releases as well as assisting Quality management with department needs. Essential Functions and Responsibilities Ensures that all procedures and processes meet internal quality standards as well as external regulations specific to pre-clinical, clinical and commercial manufacturing. Read, understand and follow all cGMP and cGTP documentation for Quality System Functions (SOPs,WIs,etc.) Maintain cGMP and cGTP compliance for all aspects of pre-clinical, clinical and commercial manufacturing. Release raw material in ERP...

Adminstrator West Bend, Wisconsin rec #REC10020234 | Updated: Within 24 hours OPENINGS: 1 JOB TYPE: Direct Hire LOCATION: West Bend, Wisconsin, United States, 53095 INDUSTRY: Medical / Healthcare SALARY: $90,000.00 - $100,000.00 / year CATEGORY: Healthcare EDUCATION: Bachelor's Degree EXPERIENCE: 2-5 years TRAVEL: Never RELOCATION ASSISTANCE: Yes - Nationwide relocation offered WORK ELIGIBILITY: Green Card, US Citizen FEES: 10% of Salary CANDIDATE GUARANTEE TERMS: 90 days PAYABLE TERMS: 90 days DATE UPDATED: Within 24 hours DATE POSTED: Sep 16, 2020 JOB DESCRIPTION POSITION SUMMARY: The Administrator of Home Based Community Services oversees all outreach services offered to the greater community to provide consistency in application of corporate policies and procedures and efficient resource utilization. The...