Quality Assurance Specialist
LanceSoft Inc
Quality Assurance SpecialistLocation: Lexington, MADuration: 3 years ContractThis is HYBRID jobResponsibilities include but not limited to:Analysis, design, build, run test cases to support new functionality or existing versions and maintain documentation of test results to assist in debugging and modification of software.Plan, design, deploy, maintain and troubleshoot related to QA tools like Tricentis TOSCA and Impact Analysis/Live Compare tool for SAP.Analysis of test results to ensure existing functionality, identify improvements as well as work with development engineers to resolve issues.Candidates should have strong Analytical background with a familiarity of working with Enterprise Resource Management System. Good knowledge of writing SQL queries against a variety of data sources. Experience in testing Web, standalone and ERP(SAP or others) applications.Must Have:Should have demonstrated a pragmatic and disciplined approach in successfully implementing best SQA practices in a "real world" company.Technical education and solid technical knowledge (e.g. Degree or equivalent technical experience)Prior use of test management tools (ex. Jira)Bug Identification and TrackingCreating Test ScriptsDefine Test StrategiesDevelop Test PlansMonitor Testing ProceduresSoftware TestingSoftware ValidationTest-driven, Unit TestingTesting and EvaluationTest Procedure CompositionTest Matrix ConfigurationExcellent written and verbal communication skillsAbility to work as part of a distributed teamSelf-starter with the ability to determine technical solutionsExperience with Tricentis TOSCA tool and Impact Analysis/Live CompareNice to have:Knowledge of Sysinternals tools to support system diagnosticsSAP/ERP technical product experience is preferred, for example, any aspect of quality assurance, software development, systems architecture, or administration on these toolsKnowledge of ServiceNow a plusEEO Employer LanceSoft is a certified Minority Business Enterprise (MBE) and an equal opportunity employer. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. LanceSoft makes hiring decisions based solely on qualifications, merit, and business needs at the time.
- Job DescriptionDescriptionThe Quality Assurance Professional will work in the US External QA team responsible for Contract Manufacturing (CMO) and Contract Test Laboratories (CTL) oversight within the Biologics Operation Unit Quality Assurance Department . This unit oversees...SuggestedContract workFlexible hours
- What You’ll DoThe Senior Quality Assurance Specialist provides quality assurance oversight across CMC development, Quality Control, Analytical Development, manufacturing, and supply chain activities, ensuring compliance with global regulatory requirements and internal...SuggestedFull timeContract workImmediate start
- ...Quality Assurance SpecialistIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission...Suggested
- ...Senior Quality Assurance SpecialistLantheus is headquartered in Bedford, Massachusetts with offices in New Jersey, Canada, and Sweden. For... ...Summary of roleLantheus is seeking a Senior Quality Assurance Specialist to provide Quality Assurance expertise for the QA/QC,...SuggestedMonday to FridayNight shiftDay shiftAfternoon shift
$28.85 - $34 per hour
...organization and time management skills. Proficient in MS Word and Excel Experience with electronic batch records, ERP systems and Quality Management Systems (Examples: TrackWise and Veeva). WORKING CONDITIONS AND PHYSICAL DEMANDS Ability to lift and transport up...SuggestedHourly payFor contractorsWork at officeMonday to FridayWeekend work$85k - $105k
Quality Assurance Specialist II, Device Engineering Location: Woburn, MA (relocating to a new facility in Allston next year)Schedule: Onsite 5 days/week with future hybrid flexibility following relocationCompensation: $85,000 - $105,000 base salary + bonus + stock optionsJoin...Relocation- ...Seeking a quality professional with 4+ years of GMP experience in the pharmaceutical/biopharmaceutical industry to support quality oversight of external manufacturing and testing activities for clinical-stage products. Responsibilities include reviewing batch records,...Work at office
$65 - $75 per hour
...Join to apply for the Quality Assurance Specialist role at Veritas Search Group This range is provided by Veritas Search Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $65.00/hr - $75.00/hr Direct...Contract work- ...The Quality Assurance Specialist will actively contribute to the implementation and maintenance of the Quality Systems Manual and conduct GMP compliance audits as directed. The QA Specialist will have oversight of and involvement in, GMP compliance for production of Clinical...Contract work
$86.57k - $112.54k
...Title: Senior Quality Assurance Specialist - Multifamily Division Organization: MassHousing Posting Closes : Close of Business on August 18, 2026 Website: The Organization MassHousing will confront the Commonwealth's housing challenges to improve the lives of its people...Contract workTemporary workWork experience placementWork at officeShift work$25 - $27 per hour
...Quality Assurance AssociateWe are seeking a Quality Assurance Associate to support on-the-floor QA issues within the manufacturing suite. This role requires mitigating gaps and risks for all quality and GMP processes, running investigations for deviations, change controls...Temporary work$100k - $115k
...you can be part of that team. JOB SUMMARY In support of biologics/gene therapy manufacturing operations, the Senior Quality Assurance Specialist champions collaborative day to day floor support, batch record review, and batch disposition. This role is accountable...Live inVisa sponsorshipShift work- ...values and are passionate about delivering outstanding customer service, we want to hear from you! We’re seeking a Quality Assurance Specialist who: Demonstrates reliability and flexibility with changing work schedules. Is open to transitioning between different...Remote workWork from home
- Vericel Corporation, a leader in advanced cell therapies, seeks a QA-focused professional for day-to-day batch record review, labeling, archiving, and final product inspection in our Burlington, MA facility. You'll gown into ISO 7 clean rooms and support release activities...RelocationWeekend work
- ...Manufacturing, Regulatory Affairs etc) to confirm the appropriate quality as well as compliant controls are in place for assigned Gene... ...quality systems Support batch disposition and release Quality Assurance Lead for the cross-functional CMC Sub-Teams Provide quality...Contract workLocal area
- Charles River Center in Needham, MA is seeking a Quality Assurance Associate - CBDS & Employment Services to support the Director of Quality Assurance in ensuring compliance, quality, and continuous improvement across community-based day supports and employment services...
- Ultragenyx Pharmaceutical in Bedford, MA seeks a Quality Assurance Drug Substance (DS) Specialist to oversee QA activities for a gene therapy manufacturing site. You will review batch records, perform deviations management, and collaborate across Manufacturing, Engineering...
$50 - $55 per hour
...poster from Software Guidance & Assistance, Inc. (SGA, Inc.) Software Guidance & Assistance, Inc., (SGA), is searching for a Quality Assurance Specialist for a contract assignment with one of our premier BioTech services clients in Boston, MA . Responsibilities : The firm...Full timeContract workFor subcontractorCasual workShift work- ...Vertex Inc. is seeking a Clinical Study Quality Lead (SQL), Associate Director to oversee advanced GCP quality assurance across clinical trials and vendors. You will design and execute quality plans, assess compliance risks, and drive inspection readiness while collaborating...
$143k - $155k
...: Position Summary: Cross-functional to support relevant Quality Systems GXP activities in adherence to applicable regulations (... ...experience in pharmaceutical/ biotech industry within Quality Assurance or Quality (Assurance) exposure, or equivalent experiences Or...Work at officeFlexible hours- ...seeking a CMC QA Consultant to support cross-functional teams across PD, MSAT, CMC, Manufacturing and Regulatory Affairs to ensure quality and compliant controls for gene therapy programs. You will review batch records, deviations, tech transfers, and regulatory submissions...
- ...patients.Position Summary: Cross-functional to support relevant Quality Systems GXP activities in adherence to applicable regulations (... ...experience in pharmaceutical/biotech industry within Quality Assurance or Quality (Assurance) exposure, or equivalent experiencesOr, Associate...Work at officeFlexible hours
$98.5k - $109.1k
...complex principles and practices of cell processing and experience as an auditor and compliance specialist. The QA/QI Specialist is responsible assisting in the monitoring for quality to ensure that systems are appropriate, current and being adhered to by all staff of the...Full timeFlexible hoursShift workWeekend work- Furnished Quarters in Charlestown, MA, is seeking a Guest Operations Specialist to uphold cleanliness and appearance standards across multiple apartment sites. You will inspect units, test equipment, and ensure design standards are met, collaborating with housekeeping...
- Ultragenyx Gene Therapy in Bedford, MA is seeking a Senior Specialist, Quality Assurance Operations to oversee QA activities for drug substance manufacturing at a new gene therapy facility. You will review batch records, manage deviations, and support manufacturing approvals...
- ...Binding Minds Inc. is seeking a quality professional in Boston with over 4 years of GMP experience in the pharmaceutical industry. The role involves quality oversight of external manufacturing and testing activities for clinical-stage products, requiring strong knowledge...
- ...QA Specialist Perform the QA review/approval of analytical documentation: Analytical method validation protocols and reports for in-process and release/stability testing Analytical method procedures and associated change controls Method technical transfer protocols...
$40 - $55 per hour
This range is provided by Insight Global. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $40.00/hr - $55.00/hr The Engineer is actively involved in Commissioning, Qualification, Validation, and Requalification...Contract work- ...world. What You Will Be Doing: The Audit Specialist at Trial Interactive is responsible for... ...audit findings, ensuring compliance to quality standards, and leading efforts to enhance... ...Required Skills: Proficient in quality assurance (QA) processes and audit management. Excellent...Full timePart timeInternshipLocal area
$110k - $120k
...requirements across manufacturing, testing, product disposition, and quality event management. This role is part of a small QA team with... ...primates. Characterizing Your Impact: As the Senior QA Specialist, you will: Maintain Quality oversight of GMP operations...Flexible hours
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