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Roche

Global pharmaceuticals and diagnostics company

QS&C Associate Manager System Digitalization

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeShanghai, ChinaNo salary listedIn-person

About the Job

Requirements

  • A minimum of 4 years of experience in pharmaceutical or biotechnology quality assurance, GMP compliance, operations, or validation is required; multinational-company experience is ideal.
  • Experience with regulatory inspections by Health Authorities and representing the company in interactions with Health Authorities, their agents, or related entities.
  • Good knowledge of relevant EU GxP and Quality System requirements for pharmaceutical and biotechnology manufacturing and related activities.
  • Hands-on experience with SAP and Veeva.
  • Knowledge of current Good Manufacturing Practice (cGMP), a thorough understanding of International Council for Harmonisation (ICH) guidelines, and exposure to the international network.
  • Aseptic filling experience is expected.
  • Fluent English communication skills and the ability to communicate and collaborate effectively with team members and stakeholders.
  • The candidate should have at least a degree in pharmaceutical sciences, life sciences, biology, biotechnology, chemistry, chemical engineering, or a related discipline.

Responsibilities

  • Support mobilisation of new sites from a quality and compliance perspective.
  • Lead or support local implementation of global quality computerized projects, including master data readiness, end-to-end scenario test preparation and execution, standard operating procedure establishment or revision, end-user knowledge sharing, and hypercare incident troubleshooting to ensure a smooth go-live.
  • Lead master data maintenance in daily operations on quality computerized systems, including master data management, timely issue resolution, and maintenance of S/4 and BRH system execution procedures and business continuity plans.
  • Identify, assess, and escalate potential quality risks in computerized system modules, and develop practical mitigation strategies and solutions to keep systems running smoothly and meet business needs.
  • Serve as a key contact for computerized system quality modules and provide technical and process support to cross-functional business partners.
  • Collaborate to resolve computerized system quality-module issues, remove technical barriers, and ensure delivery of project and system objectives.
  • Provide ongoing operational and maintenance support for computerized system quality modules after go-live; assess business suitability of system processes, gather user feedback, and lead process enhancements and continuous-improvement initiatives to support evolving business needs.
  • Perform other duties as assigned by the line manager.

Desired Qualifications

  • Multinational-company experience in pharmaceutical or biotechnology quality assurance, GMP compliance, operations, or validation.

About the Company

Roche

Global pharmaceuticals and diagnostics company

Roche is a global leader in pharmaceuticals and diagnostics. It develops medicines and diagnostic tools that help detect, monitor, and treat diseases, using research and biotechnology to drive new therapies and tests. Roche combines drug development with in-house diagnostic products to support personalized medicine, where treatments are tailored to individual patients based on test results. Its approach differs from many peers by integrating drug discovery with diagnostic capabilities and by expanding its research through strategic acquisitions (like Genentech) to strengthen its biotechnology and R&D capabilities. The company’s goal is to improve patient outcomes and healthcare worldwide by delivering reliable medicines, accurate diagnostic tests, and data-driven care.

Company size
1-10
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1896

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