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Sanofi

Global pharma company; vaccines and R&D

Buffer, Media & Utilities Team Lead Tank Farm

Full-TimeUpdated on 10/23/2026Deadline 12/5/26
No salary listed
Mid
Bachelor's, Master's
Beijing, China
In Person
Biology & BiotechBioprocess & Biomanufacturing

About the job

Requirements
  • A bachelor's or master's degree in chemical engineering, biotechnology, bioengineering, or related education is required.
  • More than three years of industrial experience in the pharmaceutical business is required.
  • A technical background in operating large-scale chemical or biochemical equipment is required.
  • Knowledge of current Good Manufacturing Practice (cGMP) and regulatory requirements is required.
  • Ability to work as part of a team in a continuously changing project environment is required.
  • Ability to manage the complexity of many interfering activities is required.
  • Ability to work in a highly matrix-driven project environment with strong functional reporting lines is required.
  • Leadership capabilities for functional and direct-reporting teams are required.
  • Strong technical networking capabilities are required.
  • Ability to collaborate closely and build cross-functional bridges is required.
  • High-level communication skills are required.
  • Good written and spoken English skills are required.
Responsibilities
  • Represent Buffer, Media & Utilities know-how and operational knowledge in the project team, focusing on systems that support the insulin process from large-volume fermentation in Upstream through final purification in Midstream and Downstream.
  • Support and oversee project tasks during engineering and construction phases, including planning and design, P&ID review, and HAZOP.
  • Support harmonization of processes and technologies between the Frankfurt and China facilities.
  • Partner with engineering throughout project phases by reviewing and approving equipment and system designs, supporting vendor selection and equipment procurement, developing standard operating procedures and operational documentation, supporting staff training program development, participating in equipment and system commissioning, establishing process-related user requirements, and participating in C&Q/OQ/PQ/PPQ.
  • Ensure biologics product quality standards and regulations are implemented in the area of responsibility.
  • Support implementation and translation of process-control, microbial and contamination-control, filter, and single-use strategies into operational processes.
  • Participate in and support interactions with authorities.
  • Build the tank farm operational team and support strategic workforce planning.
  • Partner with MSAT on technology transfer and scale-up activities and collaborate across highly cross-functional teams.
  • After commissioning, coordinate and organize a team of up to 10 people to secure liquid raw material supply throughout production.
Desired Qualifications
  • Experience leading and upskilling teams, talent management, and knowledge transfer is desirable.

About the company

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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Simplify's Take

What believers are saying

  • July 10, 2026 FDA approval of Sarclisa Escena created the first on-body cancer injector.
  • June 13, 2026 FDA accelerated approval expanded Tzield into recently diagnosed stage 3 T1D.
  • Q2 2026 sales grew 17.8% at CER, with Dupixent and Beyfortus leading.

What critics are saying

  • Texas sued Sanofi on February 19, 2026 over provider bribery and Medicaid fraud.
  • Sanofi sued Pfizer and Moderna on July 15, 2026, extending costly mRNA patent warfare.
  • Dupixent concentration makes 2030s patent loss an existential revenue shock.

What makes Sanofi unique

  • Dupixent reached €5.2 billion quarterly sales in Q2 2026 across nine indications.
  • October 1, 2026, Sanofi and Regeneron added four long-acting antibodies to their Alliance.
  • Sanofi's 61-project pipeline spans immunology, rare diseases, vaccines, neurology, and oncology.

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Benefits

  • Health Insurance
  • Professional Development Budget
  • Parental Leave

Company News

Associated Press
Oct 19th, 2026
Enable Injections wins first Japan approval for enFuse on-body injector via Sanofi's CirCLIQ

Enable Injections has won its first commercial product approval in Japan. The country's Ministry of Health, Labour and Welfare approved the company's enFuse On-Body Delivery System through Sanofi's CirCLIQ Injector. The device delivers a subcutaneous form of Sarclisa (isatuximab) with the push of a button, for treating multiple myeloma. It is the first anticancer treatment given through an on-body injector in Japan. The approval follows recent clearances in the US and Europe. Japan approved Sarclisa SC in June 2026, backed by the IRAKLIA phase 3 study, which showed the subcutaneous form was non-inferior to intravenous delivery. "We're proud to partner with Sanofi to bring our enFuse technology to patients in Japan," said Michael D. Hooven, chairman and chief executive officer of Enable.

Yahoo Finance
Oct 1st, 2026
Sanofi, Regeneron expand alliance in up to $8B deal for immunology drugs

France's Sanofi and US-based Regeneron Pharmaceuticals will expand their 20-year partnership to jointly develop and market immunology medicines in a deal worth up to $8 billion. Regeneron will receive $1 billion upfront, with potential additional payments of up to $7 billion tied to development, regulatory, and commercial targets. The collaboration will add four next-generation immunology drug candidates invented by Regeneron, with one currently in early-stage trials for eczema. The companies will equally share development costs and future profits from new drugs, whilst their existing profit-sharing agreement for top-selling medicine Dupixent remains unchanged. The deal settles prior litigation between the companies and marks an early move by Sanofi's new chief executive Belen Garijo to strengthen the company's pipeline.

Sanofi
Sep 20th, 2026
Press Release: Sanofi completes acquisition of Vicebio

Sanofi completes acquisition of Vicebio Paris, December 4, 2025. Sanofi announces the completion of its acquisition of Vicebio Ltd (“Vicebio”). This acquisition brings an early-stage combination...

Sanofi
Sep 20th, 2026
Press Release: Sanofi completes acquisition of Blueprint Medicines

Sanofi completes acquisition of Blueprint Medicines Paris, July 18, 2025. Sanofi today announces the completion of its acquisition of Blueprint Medicines Corporation (Blueprint), adding to its...

Sanofi
Sep 20th, 2026
Press Release: Sanofi completes the acquisition of Dynavax

Sanofi completes the acquisition of Dynavax Paris, February 10, 2026. Sanofi today announced that it has completed the acquisition of Dynavax Technologies Corporation (Dynavax). The acquisition...