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Sanofi

Global pharma company; vaccines and R&D

Biotechnologist Trainee - Career Conversion Program

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeSingaporeNo salary listed

About the Job

Requirements

  • NITEC or a Diploma in an Engineering or Science discipline.
  • Be able to work in a twelve-hour rotating shift pattern consisting of day and night shifts.
  • Be able to operate and perform in cross-functional teams.
  • Have analytical and critical-thinking skills and the ability to problem-solve and navigate complexity and ambiguity.
  • Be able to work in fast-paced and dynamic conditions with tight timelines.
  • Have presentation and verbal communication skills and be able to adapt communication to various stakeholders.
  • Have technical writing skills.

Responsibilities

  • Execute routine current Good Manufacturing Practice manufacturing activities within the Upstream, Downstream, or Central Manufacturing Services (Media & Buffer, Logistics) teams, in accordance with process, quality, and safety standards.
  • Operate and monitor manufacturing equipment, digital systems, and automation systems during day-to-day production runs.
  • Perform general housekeeping of manufacturing areas.
  • Maintain regulatory and audit readiness through adherence to procedures and documentation standards.
  • Act as a key user of digital and automation applications and software supporting manufacturing systems, including enterprise resource planning, manufacturing execution systems, and process control systems.
  • Participate in continuous-improvement and optimization initiatives to enhance routine operational efficiency.
  • Support batch documentation, deviation reporting, and change-control activities as part of routine operations.
  • Perform day-to-day production activities within Upstream, Downstream, or Central Manufacturing Services, ensuring compliance with process, quality, and safety requirements.
  • Maintain and follow standard operating procedures, risk assessments, and training records for manufacturing equipment and systems.
  • Operate and troubleshoot digital and automation tools integrated into daily manufacturing processes.
  • Support routine batch production, in-process checks, and quality documentation in line with current Good Manufacturing Practice standards.
  • Identify and contribute to process-optimization opportunities within the assigned Upstream, Downstream, or Central Manufacturing Services area.

Desired Qualifications

  • Prior internships or industrial attachments in biopharmaceutical or biotechnology organizations are advantageous.

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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