Sr Lead QA Analyst

Integrated Resources, Inc

Cambridge, Massachusetts

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JOB DETAILS

JOB TYPE

Contractor

SKILLS

Analysis Skills, Clinical Research, Code of Federal Regulations, Communication Skills, Consulting, Corrective Action, Cross-Functional, Detail Oriented, Documentation, FDA (Food and Drug Administration), GxP, Information Technology & Information Systems, Interpret Regulations, Maintain Compliance, Multitasking, Organizational Skills, People Management, Presentation/Verbal Skills, Quality Assurance, Regulations, Regulatory Compliance, Rehabilitation Nursing, Risk Analysis, Risk Management, Schedule Development, Software Development Lifecycle (SDLC), Software Testing, Standard Operating Procedures (SOP), System Lifecycle, System Validation, Systems Analysis, Systems Maintenance, Technical Leadership, Technical Support, Training/Teaching

LOCATION

Cambridge, Massachusetts

POSTED

1 day ago

Sr Lead QA AnalystA Few Words About Us Integrated 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 centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionPrincipal Duties & Responsibilities:Approve system life cycle deliverables and activities to ensure that regulations, protocols, procedures, and methodologies are followed, and that appropriate and complete documentation is captured and reported to support validation activities.Represent IT Quality & Regulatory Compliance on cross-functional teams in support of SDLC activities.Consult on the authoring and conformance of validation-related deliverables and activities in regard to corporate SOPs and current regulations.Provide guidance, training, and support to IT personnel in their validation efforts, to ensure compliance.Provide quality assurance oversight for system related issues (deviations, incidents, etc.)Assist in the development of IT ControlsAdvise technical personnel and management on regulatory compliance and interpretation and recommend appropriate corrective actions where needed.Job Demands: This job requires the Quality Assurance and Validation Specialist to attend department and user meetings, system assessment meetings, trainings, and other essential tasks. The Quality Assurance and Validation Specialist must maintain a professional manner in representing the company and in working with its agents and associates. The Quality Assurance and Validation Specialist should demonstrate initiative and self-direction while also knowing when to seek assistance. This person must also be able to routinely schedule and complete multiple tasks and be timeline driven.Job Impact: The Quality Assurance and Validation Specialist's role is essential in maintaining systems that are compliant with both regulatory (e.g., FDA) and corporate requirements and good business practices.QualificationsQualifications:Thorough knowledge of GxP and ERES (21 CFR Part 11 and Annex 11) regulations and guidelinesThorough knowledge of IT Controls methodologies, including GAMP5 and ITILExcellent communication skills, both verbal and writtenDetailed knowledge of the IT system development life cycle and software quality assurance in a regulated environmentKnowledge of general software and database conceptsExperience with risk analysis and risk management practices and toolsKnowledge of infrastructure technology and platformsThe ability to work both independently and with teams at various levels in the organizationExcellent organizational skills and attention to detail and accuracyFive or more years of experience in computerized system validation within a regulated environment

Sr Lead QA Analyst

Integrated Resources, Inc

Cambridge, Massachusetts

About the Company

Integrated Resources, Inc

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