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Sanofi

Global pharma company; vaccines and R&D

M&S Graduate Program-Operation (Production) Lead

Manufacturing & Production OperationsConfirmed live in the last 24 hours
Full-timeHangzhou, Zhejiang, ChinaNo salary listedIn-person

About the Job

Requirements

  • At least 2–3 years of experience in production, manufacturing, or quality management within the pharmaceutical industry.
  • A STEM background is strongly preferred, including Pharmaceutical Engineering, Chemical Engineering, Biotechnology, Life Sciences, or related technical disciplines; a top MBA with relevant manufacturing exposure is also considered.
  • Master's degree or above.
  • Intermediate IT skills.
  • Negotiation skills.
  • Leadership skills.
  • Management skills.
  • Lean management skills.
  • Communication skills.
  • English language proficiency.

Responsibilities

  • Support daily production operations and progressively develop root-cause analysis capability for technical deviations, building toward independent ownership by Year 2–3.
  • Learn to organize and manage manufacturing resources, balancing facility and equipment capacity, workforce, and production cost under senior guidance.
  • Contribute to process optimization initiatives, including parameter refinement and equipment adjustment, to enhance quality and output.
  • Support the planning and execution of process validations to ensure quality stability through process changes, progressively taking ownership of validation projects.
  • Implement current Good Manufacturing Practice (cGMP) practices in daily operations, aligned with global standards.
  • Take accountability for Health, Safety, and Environment (HSE) within the assigned scope, learning to allocate resources for risk assessment, training, and safety program execution.
  • Participate in deviation, out-of-specification (OOS), and complaint investigations alongside cross-functional teams, and follow up on Corrective and Preventive Action (CAPA) implementation.
  • Support change control, equipment and cleaning validation, and batch record and standard operating procedure (SOP) authoring and review.
  • Progressively build and develop a professional production team, strengthening peers' GMP awareness and technical capability.
  • Lead cross-departmental projects, applying influence, planning, and execution skills.
  • Ensure compliance with psychotropic drug safety management regulations, report abnormalities promptly, and complete required certifications.

Desired Qualifications

  • Experience in foreign or multinational manufacturing environments is a strong plus.

About the Company

Sanofi

Global pharma company; vaccines and R&D

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company size
10,001+
Company stage
IPO
Headquarters
Paris, France
Founded
1973

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