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Roche

Global pharmaceuticals and diagnostics company

GMP Orgmp

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

About the Job

Requirements

  • A bachelor's degree or higher is required.
  • At least 5 years of operational experience in GMP compliance roles in the injection pharmaceutical industry is required.
  • Strong knowledge of current good manufacturing practice and regulations relevant to the pharmaceutical industry, especially the biological industry, is required.
  • Hands-on experience in deviation handling, corrective and preventive action management, change control, and audit preparation is required.
  • Familiarity with compliance tools and systems for managing training, deviations, and corrective and preventive actions is required.

Responsibilities

  • Collaborate with cross-functional teams to implement GMP-related systems, processes, and workflows for the production department.
  • Develop and implement GMP training programs tailored to production staff and aligned with corporate quality policies and regulatory requirements.
  • Establish deviation management and corrective and preventive action processes in manufacturing to handle non-conformances and ensure timely resolution.
  • Implement a change control process that ensures GMP compliance and proper documentation of changes in the production environment.
  • Participate in preparation for facility qualification audits and regulatory inspections, ensuring systems and practices meet GMP standards.
  • Lead consumable materials and service introduction and track status to meet manufacturing requirements.
  • Support development of GMP documentation, including standard operating procedures, validation protocols, and project-specific documentation for compliance.
  • Perform other duties as assigned.
  • Ensure routine operation complies with Roche's GMP, safety, health, and environmental requirements and applicable regulations.
  • Serve as the primary interface between the production department and quality assurance and compliance teams for GMP-related matters.
  • Manage ongoing GMP training programs and ensure production personnel are regularly updated on GMP and compliance requirements.
  • Oversee timely identification, investigation, and resolution of deviations and proper execution of corrective and preventive actions to prevent recurrence.
  • Evaluate and coordinate changes within the production department, ensuring proper implementation and documentation in line with regulatory requirements.
  • Act as the production department's primary liaison during internal and external audits, ensuring inspection readiness and addressing observations.
  • Monitor GMP compliance in daily operations, identify gaps, and implement corrective actions.
  • Identify areas for improvement in GMP operations and drive initiatives to enhance quality and productivity while maintaining compliance.
  • Perform other duties as assigned.

Desired Qualifications

  • A pharmaceutical or biological field of study is preferred.
  • Experience in strategic facility projects, including design, commissioning, and qualification, is preferred.
  • Experience in multinational biopharmaceutical companies is preferred.
  • Fluent English communication skills are preferred.

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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