Senior Supply Chain Operations – Life Sciences Manufacturing Quality

. Assess quality and laboratory workflows, user needs, system interfaces, instrument and equipment data, and current-state pain points .

Posted 10/28/2026full-timeBoston • Massachusetts • United StatesSenior💰 $97,300 - $202,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in quality management systems (QMS) and laboratory workflows, with a strong focus on digital quality capabilities, data integrity, and compliance in regulated environments. Proficient in developing and implementing quality processes, documentation, and integration across various systems.

Highest-signal resume keywords

Quality Management Systems (QMS)GxP/GMP ComplianceLaboratory Data IntegrationCAPA and Deviation ManagementFunctional and Integration Testing

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Quality Process DocumentationData Mapping and Quality RulesConfiguration and Integration of eQMS/QMSTechnical Delivery Artifacts ProductionLaboratory Instrument ConnectivityRoot-Cause AnalysisAI Applications for QualityTest Script DevelopmentChange Control ManagementSupplier Quality Management

Soft Skills

CommunicationCollaborationProblem-SolvingAnalytical ThinkingProject Coordination

Tools & Technologies

LIMSEQMS/QMS PlatformsMESERP SystemsChromatography Systems

Industry Keywords

Life SciencesPharmaceuticalBiotechnologyMedical DeviceRegulated Environment

Tech Stack

Tools & technologies

ERP

About the role

Key responsibilities & impact

Assess quality and laboratory workflows, user needs, system interfaces, instrument and equipment data, and current-state pain points
Document process flows, user stories, functional requirements, data mappings, interface requirements, quality-system controls, and acceptance criteria
Support design and implementation of digital quality capabilities covering deviations, investigations, CAPA, change control, complaints, audits, supplier quality, batch disposition and release, review by exception, and quality risk management
Design and improve eQMS/QMS workflows, including configuration, records management, approvals, escalations, effectiveness checks, reporting, and integrations
Connect QA/QC and laboratory processes across LIMS, eQMS/QMS, MES, ERP, chromatography, laboratory data, and manufacturing systems
Develop and review quality and laboratory data models, source-to-target mappings, data-quality rules, and contextualized datasets
Work with architects and engineers on interface specifications, APIs, laboratory-instrument connectivity, and secure data movement
Configure or prototype solution components and document design decisions
Prepare and execute functional and integration test scripts, record defects, support retesting, and maintain traceability
Support deployment readiness, controlled change, user training, hypercare, and handover
Partner with quality and validation teams on GxP/GMP, data integrity, electronic records/signatures, validation, audit trails, and traceability documentation
Integrate and contextualize data to identify recurring events, detect trends, support root-cause analysis, and improve quality decisions
Contribute to governed AI applications for Quality, including investigations, root-cause analysis, anomaly detection, predictive quality, and decision support
Communicate progress, risks, dependencies, and recommendations to clients and engagement leaders; coordinate defined tasks with junior colleagues

Requirements

What you’ll need

Bachelor’s degree in life sciences, quality, engineering, information systems, computer science, supply chain, or a related discipline
At least 3 years of relevant experience in Life Sciences quality, QA, QC, laboratory systems, digital QMS, systems implementation, technology consulting, or a related field
Experience with quality, laboratory, or manufacturing processes in a pharmaceutical, biotechnology, medical-device, or comparably regulated environment
Experience with core quality processes such as deviations, investigations, CAPA, change control, complaints, audits, supplier quality, batch disposition, release, or quality risk management
Experience producing technical or functional delivery artifacts
Experience collaborating with quality, laboratory, operational, and technical delivery teams
Ability to travel as needed; travel can range from 80–100%
Must be legally authorized to work in the U.S. without employer sponsorship, now and in the future
Quality-domain expertise
Hands-on functional, configuration, integration, testing, or support experience with eQMS/QMS platforms
Understanding of LIMS, assays, stability, specifications, OOS/OOT workflows, laboratory instruments, deviation and CAPA analysis, and QA/QC/manufacturing/release connections
Ability to identify source systems, interpret quality and laboratory records, document mappings and interfaces, investigate data-quality issues, and contextualize information across domains
Ability to produce requirements, design documents, test scripts, defect records, validation evidence, controlled-change documentation, and deployment materials
Working understanding of GxP/GMP, data integrity, electronic records and signatures, controlled change, validation or risk-based assurance, audit trails, and traceability
Ability to assess recurring events, trends, root causes, analytics, and AI outputs for reliable data, controls, and human review

Benefits

Comp & perks

Medical and dental coverage
Pension plan
401(k) plan
Wide range of paid time off options
Professional growth
Personal fulfillment
Inclusive culture
Reasonable accommodation for qualified individuals with disabilities