Quality Assurance Tester Jobs in Norwood, MA

Quality Analyst Micro 3-6 Months Billerica, MA Max PR: $30.00 Perform testing on incoming materials, finished products and stability studies in QC Laboratory. Job Responsibilities Perform routine QC testing in accordance with SOPs and cGMP guidelines. Some supervision required. Perform verification of data to ensure accuracy. Perform approval upon discretion of supervisor. Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment. Utilize a range of electronic systems such as LIMS and document/equipment management software. Author SOP changes; participate in change controls, CAPAs, other quality systems. Resolve routine problems by utilizing appropriate resources. Assist in investigations. May assist on special projects as needed. Help with continuous improvement. Train on and maintain knowledge of current regulatory requirements and relevant internal procedures. Team player who can work independently with quality and attention to detail. Good communication skills both oral and written, professional conduct. Effectively and efficiently participate in assigned tasks in a quality manner. Actively promote safety rules and awareness. Reports and takes initiative to correct safety & environmental hazards. Work with potentially hazardous chemical, radiological and/or biological materials on a daily basis. Demonstrate good safety practices at all times including the appropriate use of protective equipment. *In case of absence the “Reports to” Manager above or a peer incumbent will function as a backup for this position. Education & Qualifications Typically requires 1-3 years of previous experience in the pharmaceutical industry, related GMP environment, or equivalent. Previous experience preferred. Requires a BA/BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and experience. Familiar with aseptic technique Perform routine Environmental Monitoring and utilities testing Perform sterility, microbial limits and Endotoxin testing, identify and trend microorganisms Some non-routine travel may be required. Flexibility with scheduling requirements-may include shifts, overtime, weekends and holiday coverage, including during adverse weather conditions. Must be able to lift 50 lbs.

Veeva QMS QA Lead Duration: Long Term Contract Required qualifications to be successful in this role • Bachelor's degree in Life Sciences, Computer Science, Engineering, or related field. • Minimum of 8 years of experience in quality assurance and validation within the pharmaceutical industry. • Extensive experience working with Quality Management Systems (QMS) and tools such as Veeva or Trackwise. • Strong experience with validation processes and documentation, including IQ, OQ, PQ, and use of HP ALM for test management and traceability. • In-depth knowledge of GxP, 21 CFR Part 11, and other relevant pharmaceutical regulations. • Proven ability to lead and manage both offshore and onshore validation and QA teams. • Excellent project management skills with the ability to manage multiple projects simultaneously. • Strong problem-solving skills and the ability to mitigate risks effectively. • Excellent written and verbal communication skills, with the ability to collaborate across different functions and regions. • Experience managing external audits and ensuring regulatory compliance readiness Manish Prabhakar Email: ****************************** Phone: ************ |VLink Inc.

QA Engineer Remote 6-Month Contract to Hire $60-70/hr $120-130K with 10% bonus Are you well-versed in hands-on experience with testing in ETL and Data warehousing? And are you looking for your next opportunity? This opportunity will enhance your skills in ETL tools like DBT and Automation tools like Validator with a company closing the gap between healthcare and financial systems. This role will be heavy within a migration project so get ready for this awesome opportunity! THE COMPANY This world-class technology, information, and internet company is modernizing the business of healthcare through its platform. This company is committed to championing Data and AI through its platform. Does this excite you? THE ROLE Testing in ETL and Data warehouses such as Snowflake. Hands-on with ETL tools like DBT. Documenting QA efforts such as acceptance criteria, Source-target mapping, RTM, test plans, test cases, test results, bug reporting, etc. Testing SQL reports, paginated reports, etc. Working independently as a full QA resource and adaptability to work in multiple teams at the same time. YOUR SKILLS AND EXPERIENCE A successful Lead Data Engineer within this role will likely have the following skills and experience: Bachelor's degree in Business Administration, Computer Science, Data Systems or Data Analysis preferred Rich experience in functional, integration, end-to-end, regression, performance, and user acceptance testing (3+ Years). Hands-on experience with testing in ETL and Data warehouse (Snowflake is preferred) (2+ Years). Experience in automation tools like Validator. Experience documenting QA efforts such as acceptance criteria, Source-target mapping, RTM, test plans, test cases, test results, bug reporting, etc. Must have worked on migration projects.

Role :: Payment test Lead Duration :: 12 Months JD : Required Qualifications: • 10+ years of Functional Testing experience with Information Technology and good understanding of the Payments Domain • Good understanding of Swift MT/MX Raw message Payment processing knowledge • Must be proficient in Agile methodology and experience with Jira • Experience in Test Deliverables in an onsite-offshore model. • Excellent coordination and communication skills. • Provide functional expertise and solutions for various business scenarios related to payments systems • Ability to coordinate with multiple stakeholders and liaison with business teams to support UAT testing. • Able to guide the Automation team to automate the functional testing flow.

Key Responsibilities: Develop and Execute Verification Protocols: Create and implement formal software verification and validation protocols based on product specifications, ensuring alignment with both user needs and regulatory requirements. Test Planning: Develop comprehensive test plans that define the scope and criteria for verification and validation, tailoring them to the specific requirements of each development cycle. Cross-Department Coordination: Collaborate with Software QA teams and other internal departments to guarantee that the product meets both functional and user expectations. This includes facilitating communication and feedback loops across teams. R&D Collaboration: Work closely with the R&D team to support activities such as data collection, issue reproduction, documentation, and the triage of problems. Provide technical expertise to ensure efficient resolution of identified issues. Functional Testing Development: Design and execute functional testing protocols, including unit tests, integration tests, white-box, and black-box testing approaches to ensure product robustness. Verification Compliance: Ensure the completeness of software verification efforts and adherence to applicable standards, including client's internal quality management system and industry regulations. Other Duties: Perform additional tasks as assigned to support the overall goals of the software development and validation process.

Title: Quality Assurance Associate 2nd Shift Shift: 2nd Shift, 3 pm to 11pm Monday through Friday Status: 6-12 month contract Hourly rate: $55 an hour Please note, this is Quality Assurance role and not a QC role. Qualified candidates must have experience working in a QA role on the manufacturing floor. Additionally, this contract cannot be done on C2C or offer sponsorship of any kind. Quality Assurance Associate This individual in this office-based role will maintain on site quality presence at GMP facility in Lexington, MA by providing support for clinical phase manufacturing, batch record review and quality issue resolution. Will also support incoming raw material/excipient release, document management and training systems. Primary function is to assure the quality of manufactured products is in compliance with all applicable regulations, guidelines and internal procedures. Responsibilities: • Proactively promote GMP, GDP, and compliance concepts. • Support incoming raw material release. • Support Supply Chain and Manufacturing with dispensing of raw material for batch production. • Support QC, Analytical Research and Development (ARD) with CoA review, approval, and filing. • Perform quality oversight of clinical phase manufacturing executional compliance with GMP, including issuance of production batch records, line clearance, QA on the floor presence, raw material, component, and in-process material checks. • Support batch documentation review, deviations/investigations, change control and issue resolution for Intermediate and Drug Product (DP) Disposition. Qualifications: Minimum of BA/BS in a science related field • Minimum of 5 years of related work experience in pharmaceutical, biotech or medical industry • Knowledge of Good Manufacturing Practices (GMPs), Good Documentation Practices and application within pharmaceutical development.

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap - Right Talent - Right Time - Right Place - Right Price and acting as a Career Coach to our consultants. Job Title: Laboratory Automation Engineer / Associate Research Scientist Location: Cambridge Crossing, MA 02141 100% onsite Work Schedule: Mon - Fri regular business hours. Duration: 12 months contract Top skills: • BS in an engineering discipline (biomedical, robotics, computer science or related field) with 1-3 years' experience programming and maintaining lab automation. • 2+ years of programming experience in Python or C#. • 2+ years of experience automating bioassay workflows screenings or cell culture. • 2+ years of experience with Cell Culture experience. Job Description: The client seeks a highly motivated associate lab automation engineer to join the Discovery Biology team in the Neuroscience Thematic Research Center (NTRC). The newly developed NTRC is dedicated to the discovery of new treatments for neurodegenerative diseases such as Alzheimer's and Parkinson's disease as well as rare diseases that affect both adults and children. We are looking for a candidate who is interested in learning advanced cell culture approaches including iPSC technology and automating these approaches to accelerate the discovery of new medicines for neurodegeneration. Responsibilities: • Work with scientists to develop, optimize and implement automated workflows for iPSC maintenance, differentiation and maintenance of differentiated neurons • Work with scientists to develop, optimize and implement automated workflows for disease modelling, target identification and therapeutic profiling • Perform lab automation operations including protocol design, run set up and break-down, error recovery, point-teaching etc. • Assist scientists with operation of automation platform, providing training and error-recovery support as needed. • Manage equipment scheduling, routine and preventative maintenance and lab consumables inventory. • Perform and record quality control tests of platform instruments such as liquid handlers, imagers, and plate readers. • Assist in maintaining data management platform. Minimum Requirements • BS in an engineering discipline (biomedical, robotics, computer science or related field) with 1-3 years experience programming and maintaining lab automation. or Molecular Biology/Biochemistry/Physics with 2+ years of relevant automation experience • Experience with liquid handling platforms such as Hamilton Microlab Vantage/STAR, Beckman Biomek i5/i7, Tecan Fluent etc. • Experience working with service engineers to troubleshoot and maximize system uptime. • Knowledgeable in instrument qualification processes. • Fast learner, adaptable and able to work effectively in a cross functional team environment. Preferred Additional Qualifications and Experience • Experience with cell culture and routine molecular biology techniques • Hands-on experience applying lab automation to support screening or stem cell related workflows • Experience with lab automation scheduling software and robotic systems such as HighRes Cellario, Hamilton's Venus Additional: Working in a laboratory setting. No hazardous materials, blood or animals.

Immediate need for a talented Quality Assurance Associate II. This is a 12+months contract opportunity with long-term potential and is located in Waltham, MA, (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: 24-51470 Pay Range: $40 - $43/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Review and approve Master Manufacturing Records, Stability Protocols and Reports, Sampling plans, and associated manufacturing documents for the timely initiation of GMP manufacturing activities. Perform QA review of Executed Batch Records. Perform QA review of Quality Records, i.e. Deviations, CAPAs, OOS etc., as they occur. Perform QA review and approval on SOPs, forms, WI, and other document types. Provide SAP support for GMID and BOM approval. Provide Quality oversight and Quality guidance to resolve compliance issues for lots of drug substance, bulk drug product, drug product and clinical materials for use in clinical trials. Ensure all requirements, stipulated in the CMO Quality Agreements, are being met. Review and Approve Analytical related documents such as Test Methods, Test Method Transfer Plans and Assessments, if needed. Participate in Quality Risk Assessments Assist with internal and external audits. Support of data analysis and metrics for Quality Council, KPls, and other reportable forums may be requested. Assume additional responsibilities as assigned. Key Requirements and Technology Experience: Key skills; Deviation, Veeva, CAPA, Batch Records Bachelor's and/or 8+ years of relevant experience Minimum 5 years of experience in Quality Working knowledge and ability to apply Quality principles and cGMPs in conformance to standards, preferably gained from working in a manufacturing, QA or QC environment. Demonstrated ability to interact and communicate effectively, both written and verbal, with peers, management, auditors, and consultants. Must have excellent attention to detail, project and time management skills, and the ability to manage multiple priorities with aggressive timelines. Preferred experience with outsourced manufacturing and testing operations Working knowledge of MS Office products including Word, Excel, Outlook, PowerPoint, and Project. Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

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Duration: 6+ months Hybrid 3 days We are seeking an experienced, hands-on Sr. Data and Application Senior Quality Assurance (SQA) Engineer. This role focuses on end-to-end quality assurance testing, covering data pipelines, API integrations, backend services, user interfaces, and automation across our Cyber AI application platform. This position plays a crucial role in ensuring the integrity, reliability, and security of the CASM platform that supports cybersecurity, vulnerability, and risk management needs. We have multiple openings for this role, and it is open to candidates with varying levels of experience. Role Responsibilities As a Sr. Data and Application SQA Engineer, CASM Platform, you will: Develop Comprehensive Test Strategies: Create and implement test plans covering E2E testing, including data source validation, API testing, data pipeline automation, user plane, backend services, GUI, and web application testing. Automate Test Workflows: Design and maintain automated test scripts for data pipelines, leveraging tools like Databricks for DQM (Data Quality Management) and ensuring data accuracy and quality from ingestion through to analysis layers. Collaborate Across Teams: Work closely with Product Owner, Data Engineers, AI Application Engineers, and DevOps teams to understand requirements, identify test scenarios, and troubleshoot issues efficiently. Data and API Validation: Conduct in-depth testing of data workflows, ETL/ELT jobs, and API integrations, verifying data integrity, transformation accuracy, and adherence to security protocols. Continuous Integration & Deployment (CI/CD): Implement and maintain CI/CD pipelines to automate testing, security scanning, and deployment for data and application workflows. Test Backend Services and SQL Workflows: Execute SQL and Python-based tests to validate database operations, backend services, and data plane consistency. Perform web application and GUI testing, ensuring alignment with CASM platform requirements. Drive Quality Assurance Standards: Lead initiatives to establish testing best practices, promote data accuracy, and enhance system reliability through rigorous, continuous testing. Monitor and Report Quality Metrics: Establish KPIs for testing effectiveness, create detailed reports on testing outcomes, and participate in defect analysis to improve testing processes. Education & Qualifications Minimum Qualifications Education: Bachelor's degree in Computer Science, Information Systems, or a related field, or equivalent professional experience. Experience: 5+ years in a quality assurance role with a focus on data and application testing, including hands-on experience in data pipeline testing, API, and backend service validation. Automation Tools: Proven experience of Databricks and test automation frameworks (e.g., Selenium, Postman) and data quality tools (Databricks DQM or similar). Programming Languages: Proficiency in SQL and Python for writing automated tests and conducting data validation. Cloud Knowledge: Familiarity with AWS services (e.g., S3, EC2, Lambda) and experience with CI/CD tools like Jenkins, GitLab, or AWS CodePipeline. Security Testing: Knowledge of SCAS, SAST, DAST/WAS, and experience within secure SDLC frameworks. Agile Methodologies: Strong understanding of Agile practices and experience in Agile/Scrum environments. Preferred Experience Test Strategy Design: Expertise in creating test strategies for data governance, data lineage, and compliance testing. Cross-functional Collaboration: Demonstrated experience collaborating with data engineering, DevOps, and application development teams. Data-Oriented Testing Skills: Experience with data warehousing and ETL processes, as well as quality management on platforms like Databricks.

Role: We are looking for a meticulous and experienced Test Engineer with experience in HL7/FHIR medical device interfacing, embedded medical device testing, and Microsoft Windows operating systems to join fast-moving software test and automation engineering team testing best-in-class Healthcare Informatics and Patient Monitoring solutions. The candidate should be detail-oriented, capable of developing functional test suites, and possess strong communication skills. Desired qualifications include proficiency in testing real-time distributed client-server applications, TCP/IP communication protocols, and Software as a Medical Device. This role involves working with the latest embedded device, Linux and Microsoft integrated development environment (Azure DevOps), using the latest automation tooling. KEY RESPONSIBILITIES: Requirements: § Experience with HL7/FHIR medical device interfacing § Detail oriented with demonstrated ability to understand and assess a complex software application or scenario with particular focus on the development and execution of comprehensive test scripts or protocols and defect (failure mode) detection § Proven ability to develop testing strategies including both automated and script based testing Understanding of OOP concepts, algorithms and data structures, as well as, test automation principles and techniques: Behavioral-driven development (BDD), Unit tests, CI/CD, etc. § 3+ years of hands-on experience performing automation or software development using C# § Experience in converting functional requirements into Gherkin scenarios. § Experienced of TCP/IP, WLAN, DNS, DHCP, and Active Directory § Good understanding of the V-model (Requirements analysis, functional analysis, functional vs non-functional requirements, component analysis) § Web applications testing § Experience in API and Micro Services testing § Develop functional test suites and test documentation / concepts § Experience with Microsoft© Windows operating systems § Experience with embedded medical device testing § Demonstrated capability to troubleshoot and triage issues § Demonstrated ability to work collaboratively in a cross-functional, cross-discipline environment § Experience working with OEM vendors in qualifying solutions that connect to larger systems § Background in patient monitoring systems-based products is preferred Required Skills: Top Skill Requirements: § Proficient testing of highly critical real-time large-scale distributed client-server applications (preferably healthcare) via automation. § Proficient in server/client base applications and environment in Windows environment setup and testing § Experience performing automation or software development using C# § Strong networking fundamentals understanding § Proficient in testing TCP/IP, WLAN, DNS, DHCP communication protocols § Experience in testing Software as a Medical device § Experience with Microsoft© Windows operating systems § Experience with embedded medical device testing § Solid familiarity with Windows XP, Windows 7 and Windows 8 § Experience with PC based hardware, peripherals and working with OEM add on solutions § Experience working within the guidelines of a Quality Management System Skills: - C# - Networking fundamentals - BDD Life at Capgemini Capgemini supports all aspects of your well-being throughout the changing stages of your life and career. For eligible employees, we offer: Flexible work Healthcare including dental, vision, mental health, and well-being programs Financial well-being programs such as 401(k) and Employee Share Ownership Plan Paid time off and paid holidays Paid parental leave Family building benefits like adoption assistance, surrogacy, and cryopreservation Social well-being benefits like subsidized back-up child/elder care and tutoring Mentoring, coaching and learning programs Employee Resource Groups Disaster Relief About Capgemini Engineering World leader in engineering and R&D services, Capgemini Engineering combines its broad industry knowledge and cutting-edge technologies in digital and software to support the convergence of the physical and digital worlds. Coupled with the capabilities of the rest of the Group, it helps clients to accelerate their journey towards Intelligent Industry. Capgemini Engineering has more than 55,000 engineer and scientist team members in over 30 countries across sectors including Aeronautics, Space, Defense, Naval, Automotive, Rail, Infrastructure & Transportation, Energy, Utilities & Chemicals, Life Sciences, Communications, Semiconductor & Electronics, Industrial & Consumer, Software & Internet. Capgemini Engineering is an integral part of the Capgemini Group, a global leader in partnering with companies to transform and manage their business by harnessing the power of technology. The Group is guided every day by its purpose of unleashing human energy through technology for an inclusive and sustainable future. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, cloud and data, combined with its deep industry expertise and partner ecosystem. The Group reported 2023 global revenues of €22.5 billion. Get the Future You Want | ***************** Disclaimer Capgemini is an Equal Opportunity Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, national origin, gender identity/expression, age, religion, disability, sexual orientation, genetics, veteran status, marital status or any other characteristic protected by law. This is a general description of the Duties, Responsibilities and Qualifications required for this position. Physical, mental, sensory or environmental demands may be referenced in an attempt to communicate the manner in which this position traditionally is performed. Whenever necessary to provide individuals with disabilities an equal employment opportunity, Capgemini will consider reasonable accommodations that might involve varying job requirements and/or changing the way this job is performed, provided that such accommodations do not pose an undue hardship. Capgemini is committed to providing reasonable accommodations during our recruitment process. If you need assistance or accommodation, please reach out to your recruiting contact. Click the following link for more information on your rights as an Applicant http://*****************/resources/equal-employment-opportunity-is-the-law Please be aware that Capgemini may capture your image (video or screenshot) during the interview process and that image may be used for verification, including during the hiring and onboarding process. Applicants for employment in the US must have valid work authorization that does not now and/or will not in the future require sponsorship of a visa for employment authorization in the US by Capgemini.

DETAILED STATEMENT OF DUTIES AND RESPONSIBILITIES: Proactively monitor systems for availability, capacity & performance and when necessary, investigates and analyze the problems/issues, assess criticality, and report out as required. Ensure issues are identified, documented, communicated, and appropriately escalated to ensure timely resolution of each request. Exercise responsibility and maintain acceptable levels of service performance in resolving issues, data collection, recording, reporting, and in maintaining controls over IT processes. Set up and configure Dynatrace dashboards to track system performance, application behavior, and user experience metrics such as response times, throughput, and error rates. Create custom alerts in Dynatrace to detect performance degradation, triggering timely resolution before impacting end users. Collaborate with technical and non-technical personnel (Agency functional experts, vendors, PMO, architects, etc.) to resolve open issues on a timely basis and update status and maintenance in ticketing system. Provide technical support for daily operations & oversee production system maintenance activities in close cooperation with our vendors. Participate in the patch management process for servers, system, and software. Support data updates and create both scheduled and ad-hoc reports using SQL and other DB tools. Develop project plan/timeline estimation and identify key milestones for the operations team. Monitor, track, and complete project tasks as required, ensuring outputs are timely, high quality, and tailored to stakeholder needs. Develop and implement “best practice” methodologies to enhance operations efficiency. Provide support associated with tracking, validation, and driving closure of PROD Batch Schedule exclusions, workarounds, defects, and data corrections. Manage the User Access Request process for Database, Monitoring Tools and other HIX system access. Manage the Digital Certificate update process in close cooperation with our vendors. Maintain the software inventory list including latest version and planned updates. Design presentations at high levels, incorporate advanced features of PowerPoint, Excel, etc. Adhere to all relevant Management policies, procedures, and standards. PREFERRED QUALIFICATIONS • Demonstrated ability to solve complex IT problems, monitoring servers and report generation. • Ability to resolve problems as they arise and handle situations expeditiously. • Must be a self-starter, have a broad technical background of systems, software, and technology, possess both critical-thinking and analytical skills and must be able to multi-task. • Proven experience diagnosing and resolving complex IT issues using performance data from enterprise monitoring tools like Dynatrace. • Familiarity with the following or other similar tools and technologies Dynatrace, QuickSight, AWS. • Basic scripting skills (e.g., Linux shell, Python) for task automation related to monitoring and reporting. • Familiarity with synthetic monitoring, log analytics, and APM (Application Performance Monitoring) best practices. • Experience creating reports using SQL and Toad or SQL Developer. Working knowledge of basic DB concepts. • Experience creating/interpreting architectural diagrams, ER diagrams and other technical documents. • Demonstrated experience with ticketing system preferably service now. • General knowledge and experience with Developing and presenting status reports, trends, and metrics. • Ability to take notes and document all user interactions and steps taken. • Excellent communication experience with technical and non-technical staff • Ability to develop and maintain effective relationships with management, vendors, end users and program team members. • Working knowledge of JIRA & SharePoint. JOB REQUIREMENTS: EDUCATION AND EXPERIENCE • Bachelor's Degree in Information Systems, Computer Science, or a closely related field • Minimum (5-8) years of analytical experience, preferably within operations and system engineering roles with a focus on performance monitoring and troubleshooting. • Experience working in a production environment with mission-critical systems, preferably in a regulated or government setting. • Proficiency with MS Office applications including Outlook, Word, Excel, PowerPoint, MS Project and Visio a plus • Deep knowledge and hands-on experience with Dynatrace.

Our company is a leader in software development, renowned for delivering high-quality, innovative software solutions. We specialize in creating products that meet the highest standards of functionality, reliability, and user experience. Our team values precision, attention to detail, and a commitment to excellence in ensuring the quality and performance of our software products. We are seeking a meticulous and experienced QA Tester to join our team. This role involves thoroughly testing software products to identify bugs, report issues, and ensure that our software meets all quality standards before release. The ideal candidate will have a keen eye for detail and a passion for delivering high-quality software. Key Responsibilities: Develop and execute test cases, scripts, plans, and procedures (manual and automated). Diagnose defects and track them from discovery to resolution. Partner with software developers to identify and fix bugs. Analyze test results, report to the development team, and advise on improvements. Review and analyze system specifications. Collaborate with QA Engineers to develop effective strategies and test plans. Execute test cases (manual or automated) and analyze results. Create logs to document testing phases and defects. Conduct post-release/post-implementation testing. Work with cross-functional teams to ensure quality throughout the software development lifecycle. Qualifications: Bachelor’s degree in Computer Science, Engineering, or a related field. Proven experience as a QA tester or similar role. Experience in QA methodology. Familiarity with Agile frameworks and regression testing. Ability to document and troubleshoot errors. Working knowledge of test management software (e.g., qTest, Zephyr) and SQL. Excellent communication skills. Attention to detail. Analytical mind and problem-solving aptitude. Strong organizational skills. Summary: Test software products for bugs and ensure quality standards are met before release, requiring attention to detail and a commitment to high-quality software. Responsibilities include developing and executing test cases, diagnosing and tracking defects, collaborating with developers and QA Engineers, analyzing test results, and ensuring quality throughout the software development lifecycle.

TekWissen is a global management consulting, technological service and outsourcing company delivering technology-driven business solutions to meet the strategically driven objectives for our numerous clients. Job Description Title : Quality Assurance Testing (Pega PRPC/PlanView) Location : Boston, MA Duration : 12 Months Pay Rate : Can Be Discussed Manual Testing team member to manage functional, Regression, Integration /interfaces, Conversion, Reports, End to End testing. Experience in Biopharma / Biotechnology / Clinical Research Organization is a plus. Experience with agile software practices and managing work across more than one project. Experience with various SDLC processes and how various QA activities and quality-centered best practices fit into such product development lifecycles. Minimum of 6-8 years of experience providing Software QA and Testing services. Experience working with offshore teams. Experience using PRPC developer portals and Rules Explorer Trained on PegaRULES Process Commander (PRPC), including both Fundamentals as well as Bootcamp. Experience using PRPC's Clipboard for testing Experience using PRPC's Performance Analyzer (PAL) to take performance readings for subsequent performance analysis Experience reviewing and verifying such PRPC rules as validation rules and service levels Experience with Project View tool - preferred Familiarity with FDA regulations such as 21 CFR Part 11 and GxP desirable. Good knowledge of SQL is must. Knowledge of HP Quality Center 10.x or higher version. JIRA exposure is a plus. Experience in Agile and waterfall methodology preferred. Good communication skills. Additional Information Thanks & Regards ----- Chris Zion ************ chris at tekwissen dot com

TekWissen is a global management consulting, technological service and outsourcing company delivering technology-driven business solutions to meet the strategically driven objectives for our numerous clients. Job DescriptionTitle : Quality Assurance Testing (Pega PRPC/PlanView) Location : Boston, MA Duration : 12 Months Pay Rate : Can Be Discussed Manual Testing team member to manage functional, Regression, Integration /interfaces, Conversion, Reports, End to End testing. Experience in Biopharma / Biotechnology / Clinical Research Organization is a plus. Experience with agile software practices and managing work across more than one project. Experience with various SDLC processes and how various QA activities and quality-centered best practices fit into such product development lifecycles. Minimum of 6-8 years of experience providing Software QA and Testing services. Experience working with offshore teams. Experience using PRPC developer portals and Rules Explorer Trained on PegaRULES Process Commander (PRPC), including both Fundamentals as well as Bootcamp. Experience using PRPC's Clipboard for testing Experience using PRPC's Performance Analyzer (PAL) to take performance readings for subsequent performance analysis Experience reviewing and verifying such PRPC rules as validation rules and service levels Experience with Project View tool - preferred Familiarity with FDA regulations such as 21 CFR Part 11 and GxP desirable. Good knowledge of SQL is must. Knowledge of HP Quality Center 10.x or higher version. JIRA exposure is a plus. Experience in Agile and waterfall methodology preferred. Good communication skills. Additional InformationThanks & Regards ----- Chris Zion ************ chris at tekwissen dot com

7+ years of IT experience Experience with Manhattan exp Additional Information All your information will be kept confidential according to EEO guidelines.

Sonsoft , Inc. is a USA based corporation duly organized under the laws of the Commonwealth of Georgia. Sonsoft Inc. is growing at a steady pace specializing in the fields of Software Development, Software Consultancy and Information Technology Enabled Services. Job Description:- Minimum of at least 2+ years of end to end testing Hands on experience in various testing methodologies, Defect Management Process, Test Strategizing and Test Planning Strong automation framework development experience, with hands on experience in any of the automation tools like UFT or Selenium Relevant domain experience in Payments, Wires, ACH File creation and processing and Treasury suite of applications like SWEEP, Lockbox, Account Reconciliation, Service Charge Analysis SWIFT, FedWire and Real Time Payments testing experience Understanding of one or more Estimation methodologies, Knowledge of Quality processes. Skills: Analytical abilities, Strong Technical Skills, Communication skills, ability to work in a multiple / diverse stakeholders environment, People coordination Experience and desire to work in a Global delivery environment Qualifications Basic Qualifications :- Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education. At least 2 years of experience within the Information Technologies. Additional Information ** U.S. citizens and those authorized to work in the U.S. are encouraged to apply . We are unable to sponsor at this time. Note:- This is a Fulltime job for you Only US Citizen, Green Card Holder, TN Visa, GC-EAD, H4-EAD & L2-EAD can apply. No OPT-EAD & H1B Consultants please. Please mention your Visa Status in your email or resume.

The Massachusetts Medical Society (MMS) is the statewide professional association for physicians and medical students, supporting 25,000 members. We are dedicated to educating and advocating for the physicians of Massachusetts and patients locally and nationally. A leadership voice in health care, the MMS contributes physician and patient perspectives to influence health-related legislation at the state and federal levels, works in support of public health, provides expert advice on physician practice management, and addresses issues of physician well-being. Under the auspices of NEJM Group, the MMS extends our mission globally by advancing medical knowledge from research to patient care through the New England Journal of Medicine , NEJM Evidence , NEJM AI , NEJM Catalyst, NEJM Journal Watch, and through our accredited and comprehensive continuing medical education programs. The world has changed, and so has the way we work. The MMS has adopted a flexible work model that allows most employees to choose where they work - at home, onsite in our Waltham or Boston office, or a combination of the two - based on their preferences and our business needs. Because what matters is the work we do, not where we do it. The Quality Assurance Tester will perform manual testing tasks as assigned by QA leads (functional testing, browser testing, and content verification), on projects for the New England Journal of Medicine, Knowledge Plus, Journal Watch, and other online products. Throughout a series of predefined releases; contribute to test case development and execution, and identify and log defects into the issue-tracking system. Assist in developing a QA Knowledge base by documenting product knowledge, and developing detailed prerequisites and back-end data conditions used to perform data integrity validation. RESPONSIBILITIES: Become familiar with quality-assurance concepts and types of testing, such as functional testing, regression testing, and performance testing. Successfully complete manual functional testing for multiple website components and functions, based on test cases and specifications provided. Develop a detailed understanding of how software defects are identified, reproduced, described, and documented in issue-tracking software such as JIRA. Develop an in-depth understanding of how to complete QA testing on multiple operating systems and web browsers. Gain experience working with a professional QA team on a complex software project and learn how QA fits into the overall Software Development Lifecycle.

1 Year Contract Hybrid Shift: Mon-Fri 8am-5pm or 9am-6pm Job Responsibilities • Reviews executed batch records and related documentation, resolves compliance issues and dispositions lots of drug substance, bulk drug product, drug product and clinical materials for use in clinical trials • Perform lot release Quality Review of manufacturing and quality control records to ensure compliance with specifications and regulations. • Ensure that all requirements, as stipulated in the appropriate QTA, have been met. • Issue/Review documentation, i.e. Deviations, CAPAs, OOS (out of spec) etc., as they occur. • Write and revise SOP, forms, WI, and any other document types • Assist with internal and external audits. • Support of data analysis and metrics for QMR, KPIs, and other reportable forums may be requested. • Assume additional responsibilities as assigned. • Issue/Review documentation, i.e. Deviations, CAPAs, OOS etc., as they occur. • Write and revise SOP, forms, WI, and any other document types • Assist with internal and external audits. • Support of data analysis and metrics for QMR, KPIs, and other reportable forums may be requested. Education & Qualifications • Bachelor's and/or 8+ years of relevant experience • Minimum 5 years of experience in Quality Assurance (Prefer Lot release experiences) • Working knowledge and ability to apply Quality principles and cGMPs in conformance to standards, preferably gained from working in a manufacturing, QA or QC environment. • Demonstrated ability to interact and communicate effectively, both written and verbal, with peers, management, auditors, and consultants. • Must have excellent attention to detail, project and time management skills, and the ability to manage multiple priorities with aggressive timelines. • Preferred experience with outsourced manufacturing and testing operations • Working knowledge of MS Office products including Word, Excel, Outlook, PowerPoint, and Project. Must Have Experience: • Bachelor's and/or 8+ years of relevant experience • Minimum 5 years of experience in Quality Assurance (Prefer Lot release experiences) - must be specific to pharm industry • PHD may be considered overqualified Nice to Have Experience: • Investigation or product complaint experience