Quality Assurance Specialist

Posted Yesterday
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Nivelles
In-Office
Senior level
Logistics • Other
The Role
The Quality Assurance Specialist will ensure product integrity by overseeing cleanroom operations, coordinating quality events, and supporting internal audits within a dynamic biotech environment.
Summary Generated by Built In

Donaldson is committed to solving the world’s most complex filtration challenges. Together, we make cool things. As an established technology and innovation leader, we are continuously evolving to meet the filtration needs of our changing world. Join a culture of collaboration and innovation that matters and a chance to learn, effect change, and make meaningful contributions at work and in communities.

 

Univercells Technology is part of the Donaldson Company. As a global provider, Univercells Technologies (UTEC) aims to achieve cost-effective viral production from R&D to commercial scales. We are committed to helping customers increase performance with minimized footprint and costs today, while anticipating the needs of tomorrow. The scale-X™ fixed-bed bioreactors are at the core of our biomanufacturing platforms. Our portfolio covers applications from small-scale R&D to large-scale GMP commercial manufacturing with the NevoLine™ Upstream platform. For further details, please visit us at www.univercellstech.com

Join a growing international biotech organization at the heart of innovation in bioreactors and control systems. As a Quality Assurance Specialist, you’ll contribute to product integrity, continuous improvement, and operational excellence.

What’s in it for you

  • A unique opportunity to work across multiple areas of QA: production, warehouse, validation, and supplier/customer interface—broader than most QA roles.
  • A dynamic and supportive team culture where your initiative, input, and hands-on mindset can directly shape daily operations and product quality.
  • Long-term contract with a competitive salary, health insurance, pension plan, meal vouchers, and growth opportunities in a fast-evolving organization.

Role Responsibilities

  • Support the release of high-quality products (single-use bioreactors, manifolds, and controllers) by reviewing batch records and ensuring quality standards are met.
  • Oversee cleanroom operations, incoming inspections, and quality control activities, ensuring compliance with internal procedures and regulatory expectations.
  • Coordinate and follow up on quality events (deviations, document reviews, change requests, CAPA), providing guidance across production, logistics, and maintenance.
  • Contribute to project workstreams by supporting validation activities (DQ, FMEA, IOQ, PQ) and approving specifications and drawings.
  • Support internal audits and quality system documentation updates while helping teams understand and apply quality processes.
  • Collaborate with cross-functional stakeholders to drive continuous improvements and deliver practical solutions in a dynamic production environment.

Minimum Qualifications

  • Fluency in both French and English (written and spoken).
  • Prior experience with single-use technologies in a production, quality or qualification role.
  • Strong understanding of quality systems (non-conformities, GMP practices, document control).
  • Ability to work independently, prioritize tasks, and adapt in a fast-paced setting.
  • Competency in Microsoft Office tools, especially Excel, Word, and PowerPoint.

Preferred Qualifications

  • Master's degree in a scientific or engineering discipline or equivalent.
  • 5+ years of experience in a quality, production, or validation role in a GxP-regulated environment (e.g., biotech, pharma, or medical devices).

Employment opportunities for positions in the United States may require use of information which is subject to the export control regulations of the United States. Hiring decisions for such positions are required by law to be made in compliance with these regulations. Applicants for employment opportunities in other countries must be able to meet the comparable export control requirements of that country and of the United States.

Donaldson Company has been made aware that there are several recruiting scams that are targeting job seekers.  These scams have attempted to solicit money for job applications and/or collect confidential information, Donaldson will never solicit money during the application or recruiting process.  Donaldson only accepts online applications through our Careers | Donaldson Company, Inc. website and any communication from a Donaldson recruiter would be sent using a donaldson.com email address.  If you have any questions about the legitimacy of an employment opportunity, please reach out to [email protected] to verify that the communication is from Donaldson.

Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

Top Skills

Excel
MS Office
PowerPoint
Word
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The Company
HQ: Bloomington, MN
14,000 Employees
Year Founded: 1915

What We Do

Donaldson Company helps solve some of the world's most complex filtration and contamination control challenges, and is one of the largest global providers of unique filtration technologies and high-quality filters and parts. Our filtration technologies and products are used every day, in a variety of industries and environments, including aerospace, agriculture, construction, food and beverage, manufacturing, mining, power generation, transportation and many more. Key to our success, our 14,000 employees support customers at sales, manufacturing and distribution centers from over 140 locations on six continents.

The filtration market continues to grow. Customers'​ needs for filtration solutions continue to evolve. And the opportunities for our products and our people continue to expand.

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