Industrialization Engineer (F/M)

Posted 2 Days Ago
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Aubagne, Bouches-du-Rhône, Provence-Alpes-Côte d'Azur, FRA
In-Office
Mid level
Biotech
The Role
Lead industrialization and transfer activities for Flow Kit products: manage DFMEA/PFMEA inputs, coordinate design verification and validation (IQ/OQ/PQ), define manufacturing and assembly processes, monitor yield and process stability, and prepare industrialization and qualification deliverables to ensure GMP-compliant, reproducible cleanroom production at release milestones.
Summary Generated by Built In
We are looking for a Industrialization Engineer (F/M) based in Aubagne.

The Industrialization Engineer Flow Kits contributes to the industrialization and transfer readiness of Flow Kit products by executing defined technical work packages and coordinating cross-functional activities to ensure products are translated into robust, manufacturable, validated and GMP-compliant production solutions at defined release milestones.

 

Grow with us - your responsabilities

  • Contribute to design and process risk management by preparing and consolidating DFMEA/PFMEA inputs with quality and engineering stakeholders, including functional analysis, manufacturability considerations and Design-for-Manufacturing principles to ensure risks are assessed and tracked prior to transfer
  • Support design verification activities by initiating and coordinating testing, analyzing results and documenting technical rationales, including validation of manufacturability assumptions and functional performance to confirm component selection and connection robustness
  • Drive execution of assigned industrialization work packages including monitoring yield, process stability, manufacturability risks and tracking readiness milestones to ensure products meet defined technical, quality and manufacturing requirements at release
  • Confirm manufacturability, process design assumptions & production requirements, industrialization assumptions and Standards of Production during prototype and transfer phases, including readiness reviews for production transfer to ensure stable and reproducible cleanroom production at defined release criteria
  • Prepare validation, assembly qualification and industrialization deliverables including definition and execution of process validation activities (e.g. IQ/OQ/PQ) by structuring technical documentation, consolidating test results and aligning inputs from engineering, quality and manufacturing to ensure validated, compliant production approval
  • Define and refine manufacturing and assembly processes, including key process parameters and production conditions during industrialization and establishing target operating ranges for yield, cycle time and process capability to ensure robust, scalable, repeatable manufacturing execution

 

 

What will convince us - your profile

  • Master’s Degree in Engineering, Life Sciences or related technical field
  • 3+ years of experience in product development, industrialization or production transfer in regulated or cleanroom environments
  • Experience in design verification, DFMEA/PFMEA and process validation (IQ/OQ/PQ) for complex products
  • Knowledge of GMP, quality management systems and manufacturing process definition (DfM / process parameters / validation)
  • Structured analytical and problem-solving skills with strong process focus and documentation discipline
  • Ability to collaborate in cross-functional and international teams with clear communication skills
  • Fluent in English

About Sartorius 

Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide. 

We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment.

Join our global team and become part of the solution. We are looking forward to receiving your application. 
www.sartorius.com/careers

Skills Required

  • Master's Degree in Engineering, Life Sciences or related technical field
  • 3+ years experience in product development, industrialization or production transfer in regulated or cleanroom environments
  • Experience in design verification, DFMEA/PFMEA and process validation (IQ/OQ/PQ) for complex products
  • Knowledge of GMP, quality management systems and manufacturing process definition (DfM / process parameters / validation)
  • Structured analytical and problem-solving skills with strong process focus and documentation discipline
  • Ability to collaborate in cross-functional and international teams with clear communication skills
  • Fluent in English

Sartorius Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Sartorius and has not been reviewed or approved by Sartorius.

  • Healthcare Strength Health coverage includes multiple medical plan options with dental, vision, HSA/FSA, EAP, and wellness resources across many locations. Quality of core medical, dental, and vision is characterized as solid.
  • Retirement Support Retirement offerings include a 401(k) with a company match highlighted in U.S. materials and employer‑verified listings. The match is characterized as generous at some sites.
  • Flexible Benefits Flexible hours and hybrid/home‑office options are available where roles and regions allow, with role‑dependent perks in some locations. Broader extras such as commuter benefits, discounts, and tuition assistance add optionality where eligible.

Sartorius Insights

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The Company
HQ: Göttingen
9,059 Employees
Year Founded: 1870

What We Do

Sartorius is a leading international partner of life sciences research and biopharmaceutical manufacturing. We help our customers #SimplifyProgress from drug discovery to manufacturing so that more people can have access to better medicine. With this, we are #PartOfTheSolution in the fight against diseases worldwide. With innovative laboratory instruments and consumables, the our Lab Products & Services division focuses on laboratories performing research and quality control at pharmaceutical and biopharmaceutical companies as well as academic research institutes. The Bioprocess Solutions division, with its broad product portfolio focusing on single-use solutions, helps customers manufacture biotech medications, vaccines, and cell and gene therapies safely, rapidly, and economically. Based in Göttingen, Germany, Sartorius also has a strong global reach with around 60 production and sales sites worldwide. We regularly expand our portfolio through the acquisition of complementary technologies. In 2023, Sartorius generated sales revenue of around 3.4 billion euros. Currently, around 14,600 employees from around 110 nations are working for customers around the globe. Join our team, partner or collaborate with us.

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