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Roche

Global pharmaceuticals and diagnostics company

Associate Manager-Filling

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeShanghai, ChinaNo salary listedIn-person

About the Job

Requirements

  • A college degree or higher is required.
  • At least 10 years of operations experience in the injection pharmaceutical industry is required.
  • At least 3 years of people management experience is required.
  • Strong knowledge of current Good Manufacturing Practice and regulations relevant to the pharmaceutical industry, especially the biological industry, is required.

Responsibilities

  • Build and retain an inclusive workforce and foster an environment that values diversity of thought and perspective.
  • Maintain an inclusive team that values diversity of thought.
  • Maintain strong partnerships with leaders to align on strategic projects and daily operations.
  • Manage department daily safety, health, and environment activities, implement site procedures and programs, achieve site and corporate safety, health, and environment key performance indicators, promote a safety culture, and improve employee safety behavior.
  • Manage team members’ performance and development to achieve organizational goals and support employees’ personal and professional growth.
  • Support the manager in building a talent pipeline and succession plans for key positions.
  • Maintain a culture of continuous improvement and model lean leadership principles.
  • Maintain a transparent, high-performance, empowering, and innovative culture.
  • Participate in new facility design and construction, including process design, equipment selection, user requirements specification review, factory acceptance testing, site acceptance testing, installation, operational and performance qualification, and aseptic process simulation.
  • Support establishment of an effective operating system aligned with Roche standards, including the manufacturing system, contamination control strategy, and people training and qualification system.
  • Lead establishment of procedures for aseptic techniques, good aseptic practices on the shop floor, and other processes for aseptic production execution.
  • Participate in implementation of the contamination control strategy in operations to establish a sustainable sterility assurance program.
  • Support the filling manager in establishing and implementing the site aseptic training program, ensuring only qualified people manufacture Good Manufacturing Practice lots.
  • Ensure the team is competent in vial washing, depyrogenation, filling and stoppering, and crimping.
  • Participate in technology transfer and collaborate with other functions to support successful manufacturing of new products.
  • Ensure routine operations comply with regulations, maintain sterile conditions, and achieve high-quality production standards.
  • Ensure manufacturing suites are ready, including housekeeping, machines, materials, documents, and other resources, to support timely product delivery within budget.
  • Arrange filling shifts, participate in operations as an aseptic subject matter expert, and review production batch records and deviations daily according to schedule.
  • Lead annual qualification of aseptic operators and provide on-the-job training to support formal technical and Good Manufacturing Practice training.
  • Oversee daily operation, monitoring, and maintenance of filling equipment to meet aseptic requirements.
  • Supervise aseptic operations during production and intervene promptly when abnormalities occur.
  • Participate as a subject matter expert in regulatory and global quality audits and inspections.
  • Raise deviations, participate in root-cause investigations, escalate as appropriate, and ensure deviations are closed within the required timeline.
  • Raise change controls and provide assessments.
  • Execute regular validation activities, such as aseptic process simulation.
  • Participate in operational excellence and continuous improvement initiatives.
  • Operate related information technology systems, including SAP, manufacturing execution systems, Veeva, and Cornerstone.
  • Perform other duties as assigned.

Desired Qualifications

  • Pharmaceutical or biological studies are preferred.
  • Experience in a multinational bio-pharmaceutical company is preferred.
  • Experience with strategic aseptic filling facility projects, including design, commissioning, and qualification of an isolator filling line, 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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