52 Quality Assurance Testing jobs

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.

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. >

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....

Functional Analyst REC10021936 Remote / Telework Quebec Updated 1d ago Fees 5% of Salary My fee % [?] 50.0% Positions 2 Type Full Time Salary $5,758,528 - $7,403,822/year My new applicants 0 My candidates submitted 0 Total invited candidates 0 Total active candidates 0 Recruiters engaged N/A Industry Business Services Category Analyst Education Associate's Degree Experience 5-7 years Travel Sometimes Relocation assistance No - Will consider candidates that relocate on their own Work eligibility - Job description Analyste Fonctionnel (Functional Analyst) (English job description at the bottom)   Détails de l'offre Lieu de travail :Québec,QC Nombre de poste(s) à combler :2 Statut de l'emploi : Permanent Horaire de travail : Temps plein Quart de travail : Jour   Description Être analyste fonctionnel chez notre compagnie, c’est avoir l’opportunité d’intervenir dans des projets d’envergure...

Senior Quality Engineer - cGMP San Jose, CA REF The Sr. Quality Assurance Engineer supports compliance with applicable regulatory requirements by maintaining an effective quality management system and implementing continuous improvements. This position is responsible for activities ranging from product development through commercialization. This is a hands-on role where the Sr. Quality Engineer will apply diversified knowledge of engineering, quality principles and practices for pharmaceutical and combination products. This position requires technical expertise in Aseptic Techniques. The Senior Quality Engineer is responsible for performing a quality role for the aseptic manufacturing, quality systems and compliance in accordance with cGMP, related company SOP’s, federal laws, guidelines, and regulations during the receipt, storage, manufacture, and distribution of products. Requirements Maintain and improve Quality System in accordance with FDA Regulations and ISO...

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...

Software Developer In Test - Mid-Level Allen, TX Job Type: Direct Placement Ref No: 22-00650 Date: January 28, 2022 Job Description - Software Developer In Test - Mid-Level SOFTWARE DEVELOPER IN TEST - MID-LEVEL DALLAS/FORT WORTH AREA - HYBRID $100K-$115K/YEAR THE POSITION: ICS is looking for a Software Developer in Test (SDET) to join our growing SaaS client's team in the Dallas/Fort Worth area! As a quality assurance engineer, you will provide a dedicated focus on ensuring software products and services function to desired specifications by defining and performing manual and automated testing to quantify software quality. WHAT YOU'LL DO: Responsible for defining functional and non functional test procedures by working with product and engineering and other teams. Planning and executing Tests within a given scrum team for a given criteria or product Responsible for quantifying and tracking software defects and assisting in completing corrective actions....

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  ...

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...

QC Microbiology Engineer III Allendale, NJ refManager qc microbiology capa fda cgmp Allendale NJ ref Experience level: Mid-senior Experience required: 10 Years Education level: Bachelor’s degree Job function: Quality Control Industry: Biotechnology Compensation: View salary Total position:  At Medicine our vision is creating future cell therapy miracles together. We are a leading global contract development and manufacturing organization dedicated to the advancement of cell and gene therapy products. We believe in the transformative potential of cell and gene therapies, and we are shaping the future of medicine. We open doors in the regenerative medicine industry for those looking to transform medicine while continuously improving an innovative, growing company   The Manager - QC Microbiology is responsible for the oversight and supervision of the QC Microbiology team at the 4 Pearl Court Minaris Allendale Facility. In this role, this person will be...

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...

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...

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...

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

Senior Java Test Engineer Jersey City, NJ ref send resume if a fit Pre screen questionnaire: 1. Describe your experience in custom java development for performing automation testing 2. What is the candidate's full legal name? 3. What date are you available to join? 4. Have you applied to DTCC in the past 6 Months? If yes, please provide details. 5. What is your work authorization status? 6. What is your desired hourly pay rate? 7. What is the candidate's birth day and month (required for submission to ): 8. What is your present location ? 9. Please share candidate's LinkedIn profile link. Prefer local candidates in Jersey first, but willing to look at Tampa candidates as well.   IMPORTANT : The candidate needs to have good java coding skills as this person will be writing codes in java for automation testing.   MUST HAVE Minimum of 6 years of related experience Bachelor's degree preferred with master’s or equivalent...

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...

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...

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...

Supervisor, QC Microbiology CDMO GMP Allendale, NJ ref Skills: Quality Control, Microbiology, CDMO, Environmental Monitoring, Method Validation, Method transfer, GMP Experience level: Mid Level (5-8 yrs exp.) Experience required: 3 Years Education level: Bachelor’s degree Job function: Quality Control Industry: Biotechnology Compensation: View salary Total position: 1 Relocation assistance: No Visa : Only US citizens and Greencard holders At Minaris Regenerative Medicine our vision is creating future cell therapy miracles together. We are a leading global contract development and manufacturing organization dedicated to the advancement of cell and gene therapy products. We believe in the transformative potential of cell and gene therapies and we are shaping the future of medicine. We open doors in the regenerative medicine industry for those looking to transform medicine while continuously improving an innovative, growing company. The Supervisor, QC...

Senior Quality Assurance Engineer - Medical Device San Jose, CA ref Skills: Quality Assurance, Engineering, Medical Device, • Experience with FDA Quality System Regulations and ISO Standards (ISO 13485 and ISO 14971) is required, • Experience with non-conformances, CAPA, and Risk Management, • Experience in performing test method validation and Gage R&Rs;, • Extensive experience regarding root cause analysis and statistical techniques (such as Cause and Effect Analysis, Fishbone Diagram, 5 Whys, Six Sigma processes) Job description Job insights Screening questions Candidate pipeline Direct hire Your referral reward 10% of base salary Estimate: $15,050 Guarantee period: 60 days Senior Quality Engineer - cGMP Over 3 months agoSan Jose, CA Rani Therapeutics Skills: Pharmaceutical or Biopharmaceutical experience, cGMP, Qualification activities, VHP, • Experience with FDA Regulations (21 CFR part 820, part 210 and part 211) and ISO Standards (ISO...