BQ Analyst Temporary

  • Location:Pilar, Argentina

About the job

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as Production Compliance Manager within our global vaccines business, will be to drive continuous improvement in DT/PPD manufacturing by leading deviation investigations and using your findings to deliver positive change.

Main responsibilities:

  • Comply with the HSE requirements related to their activities. Identify, correct, and promptly report unsafe conditions.

  • Conduct sample analysis for IPC, IPT, AFP, and Stability tests, mainly focusing on colorimetric determinations, according to planning and adhering to the SOPs of the techniques.

  • Maintain records of all results in accordance with GMP standards.

  • Assist in verifying solution records.

  • Assist in monitoring storage equipment at specified temperatures and follow up on EMS in controlled equipment.

  • Assist in ordering coded drugs and materials from the warehouse through the SAP system, managing stock and replenishing drugs, updating minimum stocks, and disposing of waste.

  • Assist in the verification of micropipettes, leakage, and sealing.

  • Prepare labeling for BQ aliquots in laminar flow operations and other operations.

  • Manage the intake and withdrawal of samples from the chamber.

  • Conduct monthly balance of assays and samples.

  • Review control charts for colorimetric techniques.

  • Complete the required training for the position and keep the training schedule up to date.

  • Ensure the labeling of special waste generated in the sector.

  • Ensure that the laboratory has the appropriate documentation for available drugs: safety data sheets and specifications.

  • Track current documents, ensuring that only authorized and current copies of the documents in use are utilized.

  • Assist in stock control of AFP reserve samples.

About you

  • Experience : Advanced student or professional in Pharmacy, Biochemistry, Biotechnology, Chemistry, or related fields.

  • Technical skills :Laboratory techniques

  • Education : Experience in similar positions under quality standards, GMP, and safety regulations.

  • Languages : Technical English / intermediate-advanced level

Why choose us?

  • Bring the miracles of science to life alongside a supportive, future-focused team

  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally

  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks’ gender-neutral parental leave

  • Quality control

  • Play an instrumental part in creating best practice within our manufacturing facility

Pursue Progress . Discover Extraordinary .

Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

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