Internal Operations Quality Partner

Make your mark for patients 

 

To strengthen our External and Clinical Manufacturing Quality we are looking for a talented profile to fill the position of: Internal Operations Quality Partner – Braine l’Alleud, Belgium.

About the role

This position will support the manufacturing operational activities for UCB’s biological development projects.

You will work with

Internal Operations Quality Partner will closely collaborate and partner with various UCB teams, with a particular focus on working hand-in-hand with the Internal Bio Clin Manufacturing Team.

What you will do

· Work closely with Internal Bio Clin Manufacturing Team to ensure that the Quality Management System in support of product development and clinical supplies, work in a way that ensure product quality, safety and efficacy, meet regulatory requirements and expectations and operate in a fit for purpose and in a smarter way.

· Ensure quality review of master and executed batch records for drug substance supporting clinical trial studies

· Ensure specification review and release of materials used in the production of DS (Drug substance) for Clinical Trials

· Perform release of production intermediates

· Drive the continuous QA improvement process. Ensure adequate documentation processes and systems are available and followed for development projects (SOPs / Protocols / Report review).

· Plan and manage compliance tours and on the floor spot-check of the GMP area, offering quality assurance support including but not limited to inspection.

· Be partner with other departments to identify, mitigate and subsequently resolve compliance and quality issues (Investigations / deviations / out-of-specifications) that may affect UCB development activities and products.

· Support Change Control and perform the QA evaluation

Interested? For this position you’ll need the following education, experience and skills

· Bachelor’s, master’s degree or an education in a relevant scientific discipline

· Minimum of 5 years’ experience in GMP Environment.

· Fluent English communication (oral and written); any additional languages are a plus

· Solid understanding of the pharmaceutical biologics sector, including relevant technical elements of the business

· Experience with quality systems as deviations, CAPA, Change Controls.

· A good understanding of current regulatory requirements and expectations and an ability to interpret current regulations and requirements in the product development context is essential.

· Exhibit effective communication skills when interacting with stakeholders

· Capable of working independently and taking initiative

· Must be able to act in most circumstances without direct supervision and handle complex/urgent situations.

· On-site presence required (60%)

· Perform on-call duties during weekends and public holidays on a rotating basis.

· Experience with laboratory compliance and supplier qualification process is an asset

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us 

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us? 

At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.