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LabCorp

Global life sciences R&D services

Equipment Management Associate

Regulatory & Quality (Life Sciences)Posted on Nov 9
Full-timeHarrogate, UKNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in a scientific, engineering, or related discipline is required.
  • Experience in a GMP-regulated pharmaceutical, biotechnology, or life sciences environment is required.
  • Knowledge of equipment qualification, maintenance, and lifecycle management is required.
  • Experience with GMP quality systems, including deviations, corrective and preventive actions (CAPAs), and change controls, is required.
  • Strong documentation and stakeholder management skills are required.

Responsibilities

  • Oversee the full Good Manufacturing Practice (GMP) equipment lifecycle, including onboarding, qualification, maintenance, calibration, and retirement.
  • Coordinate equipment activities with internal stakeholders, service providers, and approved vendors.
  • Serve as the equipment subject matter expert, providing technical support and resolving equipment-related issues.
  • Ensure equipment complies with GMP regulations, internal procedures, and quality standards.
  • Own or support deviations, CAPAs, change controls, investigations, and audit responses related to equipment.
  • Review qualification protocols, standard operating procedures (SOPs), validation documents, risk assessments, and vendor documentation.
  • Maintain accurate, inspection-ready equipment records and lifecycle documentation.
  • Monitor equipment status and performance, ensuring timely resolution of downtime and maintenance issues.
  • Support procurement activities, including supplier engagement, quotations, and purchase requests.
  • Promote safety, compliance, and continuous improvement across equipment management processes.
  • Manage the GMP-compliant lifecycle of laboratory and manufacturing equipment, ensuring assets remain qualified, maintained, documented, and audit ready.
  • Act as the primary point of contact for equipment management activities, working with Operations, Facilities, Quality, and external vendors to ensure equipment is installed, maintained, qualified, and retired according to GMP regulations, internal procedures, and business needs.

Desired Qualifications

  • Experience supporting BioPharm, CMC, laboratory, or manufacturing operations.
  • Knowledge of equipment qualification and validation, including IQ/OQ/PQ.
  • Experience with electronic quality or maintenance management systems.
  • Familiarity with System Lifecycle (SLC) processes.
  • Experience supporting audits, inspections, or continuous improvement initiatives.

About the Company

LabCorp

Global life sciences R&D services

Labcorp provides global life sciences and healthcare R&D services, supporting pharma, biotech, and crop protection clients with testing, safety assessments, and regulatory submissions. It conducts studies ranging from basic physicochemical tests to complex inhalation toxicology and uses specialized facilities to evaluate inhaled substances and ensure regulatory compliance. Its global presence and integrated suite of services enable clients to move projects from early development to product approval within one organization. Labcorp aims to help clients bring safe, effective products to market efficiently, advancing human health and scientific research.

Company size
10,001+
Company stage
IPO
Headquarters
Burlington, VT
Founded
1976

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