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Manufacturing Engineer – Univercells Technologies (H/F/X)

April 9th 2021

At Univercells Technologies, we are on a mission to make health equally accessible to all by developing a new generation of biotech equipment (Scale-X andNevoLine).We work every day to reinvent biomanufacturing processes and develop or integrate the next innovative technologies. Through the combination of process development and engineering expertise, we create synergies to deliver game-changing production capacities to achieve our mission: Biologics available and affordable to all!

Mission Description

YOUR MISSION

  • We are looking for a Manufacturing Engineer, a passionate change-maker, that is familiar with validation processes. As a Manufacturing Engineer, you will have the responsibility to oversee processes and equipment's improvements to meet our quality standards and efficiency performance.  You will therefore leverage good manufacturing practices, lean management, as well as validation methodologies.

YOUR RESPONSIBILITIES

  • Quality support for engineering and manufacturing team
  • A quality engineer is responsible for making sure that manufacturing and technology processes are performed correctly using the right tools, materials and processes to achieve the required product quality. 
  • Manufacturing teams – ensuring that equipment and processes follow predetermined quality standards
  • The quality engineer's job to meticulously document the problem and work with other engineers to find the root cause, define the continuous plan and monitor the improvements. 
  • Continuous improvement : simplification of process and documentation 
  • Documentation owner : Investigations / support to development studies
  • Batch record
  • SOPs
  • Qualification / Validation protocols
  • URS
  • Deviations / CAPA
  • Change request
  • Risk assessment / FMEA
  • Suppliers – working to ensure raw materials and component parts meet the company’s quality standards
  • Customers – analyzing issues reported via customer feedback, maintaining records and implementing changes to manufacturing when necessary. Is process oriented and focuses on eliminating process variation by creating, revising and strictly implementing a set of tightly and precisely defined process/procedures/quality standards that when exactly followed, ensure the final quality of the productGo and see process, gemba and act in the shopfloor to coach and accompany, train, investigate with all team members (manufacturing / engineering) It aims to improve the output quality of a process by identifying and removing the causes of defects and minimizing variability in manufacturing and business processes Training on validation, define key qualification parameters and in somehow execute the protocol / documentation good practices

Candidate profile

  • Master’s degree in engineering (electro-mechanical, bioengineering, or any related majors)
  • Minimum 3 years of experience in a similar position
  • Knowledge of quality validation is a must
  • Good knowledge in GMP environment and clean room production
  • Excellent oral & written communication skills
  • Very good organizational and time & project management skills
  • Fluent in English, French is an asset

Offer

We offer a long-term contract, a competitive salary package (health insurance, pension plan, meal vouchers…) and the possibility of evolution in an international, dynamic and fast-growing company.

Contact Details

Is it appealing to you? Are you a powerful thinker combined with an efficient doer? Apply now!