Supply Chain Operations - Life Sciences Manufacturing Quality - Senior

Other locations:
Anywhere in Country

Date:
Oct 28, 2026

Requisition

Location:

Anywhere in Country

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Client-facing Life Sciences quality professional who helps design, build, test, and deploy digital solutions for regulated quality, laboratory, and manufacturing environments. The role combines practical knowledge of quality systems and QA/QC processes with hands‑on skills in digital QMS, laboratory systems, data integration, analytics, and AI-enabled quality workflows.

As a Senior in Supply Chain Manufacturing Quality, you will work with pharmaceutical, biotechnology, and medical-device clients to connect Quality Assurance, Quality Control, laboratory, manufacturing, engineering, and supply chain needs with deployable technology. You will contribute across the delivery lifecycle, from quality-process and system assessments through requirements, solution design, configuration support, testing, validation, deployment, adoption, and stabilization.

You will work directly with Quality Assurance, Quality Control, laboratory, manufacturing, regulatory, IT, data, and technology-provider teams. You will own assigned technical and functional deliverables, help resolve implementation issues, and make clear recommendations to your workstream lead. The role calls for someone who can examine a quality or laboratory workflow, trace the records, data, instruments, and systems behind it, and translate what they learn into a compliant design or testable requirement.

In this role, you will:

• Assess quality and laboratory workflows, user needs, system interfaces, instrument and equipment data, and current‑state pain points through interviews, workshops, process observation, and data review.
• Document process flows, user stories, functional requirements, data mappings, interface requirements, quality‑system controls, and acceptance criteria for digital quality solutions.
• Support the design and implementation of quality‑domain capabilities spanning deviations and nonconformances, investigations, CAPA, change control, complaints, audits and inspection readiness, supplier quality, batch disposition and release, review by exception, and quality risk management.
• Design and improve digital‑quality workflows using eQMS/QMS platforms, including workflow configuration, records management, approvals, escalation paths, effectiveness checks, reporting, and integration with adjacent enterprise systems.
• Connect QA/QC and laboratory processes across LIMS, eQMS/QMS, MES, ERP, chromatography and other laboratory data systems, and relevant manufacturing platforms; support assays, stability programs, OOS/OOT traceability, deviation and CAPA analysis, and batch‑review workflows.
• Develop and review quality and laboratory data models, source‑to‑target mappings, data‑quality rules, and contextualized datasets that relate quality events to products, materials, batches, methods, specifications, instruments, equipment, and process conditions.
• Work with solution architects and engineers on interface specifications, APIs, laboratory‑instrument connectivity, and the secure movement of quality, laboratory, manufacturing, equipment, and process data across site and enterprise environments.
• Configure or prototype solution components where appropriate to your experience and the engagement, and document design decisions for review by quality, technical, and client leads.
• Prepare and execute functional and integration test…