UCB

Downstream Biomanufacturing Process Expert

UCB$100K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Degree in a relevant scientific or engineering field, or equivalent experience in biopharmaceutical manufacturing.
  • Experience in biopharmaceutical operations and large-scale drug substance or purification projects within the pharmaceutical industry.
  • Strong knowledge of mammalian biopharmaceutical production, buffer preparation, and process operations.
  • Ability to communicate clearly, write technical documentation, and collaborate across functions.
  • Experience in regulated manufacturing environments including audits and compliance-oriented decisions.
  • Willingness to adapt to rapid project changes and evolving work environments.
  • Proficiency in English; French is an added advantage.

Responsibilities

  • Represent manufacturing in project discussions to ensure operational needs are included in facility design.
  • Translate technical and user requirements into actionable project inputs for modern manufacturing solutions.
  • Review technical documents to support decision-making for purification and filtration processes.
  • Collaborate with manufacturing sites and partners to gather operational insights and best practices.
  • Promote health, safety, environmental, and quality standards in project deliverables.
  • Stay updated on industry developments to integrate new technologies into the project.

Benefits

  • Hybrid work model promoting collaboration and teamwork at local hubs.
  • Flexible work arrangements with 40% of time in the office.
Full Job Description
Downstream Biomanufacturing Process Expert

We are looking for a Downstream Biomanufacturing Process Expert whois collaborative, proactive and innovative to join us in our BioNexUS Internal Manufacturing team, based at our UCB campus in Georgia, United-States.

About the role

This role is part of the BioNexUS project, contributing to the design and delivery of a future-ready biologics manufacturing facility. You will play an important role in a major biopharmaceutical manufacturing project, helping bring end-user knowledge into design and delivery decisions from start to finish. You will represent manufacturing needs, translate operational requirements into practical project inputs, and help ensure the future facility is designed for safe, high-quality and efficient commercial production in a rapidly evolving project environment.

Who you'll work with

You will be working in a team that partners closely with manufacturing colleagues, global cross-functional teams and project stakeholders to shape a new manufacturing facility in Georgia, United States. The team combines operational expertise, technical knowledge and strong collaboration to make sure manufacturing needs are understood, reflected in project decisions and aligned with future business needs working across different time zones.

What you'll do

  • Represent manufacturing in project discussions and ensure operational needs are reflected in facility design, systems and ways of working.
  • Translate technical, process and user requirements into clear project inputs that support practical and future-ready manufacturing solutions.
  • Review technical documents and data to support sound decisions for purification, filtration and buffer preparation processes.
  • Work with manufacturing sites and cross-functional partners to gather best practices, operational insight and lessons learned.
  • Promote strong health, safety, environmental and quality standards in daily project decisions and deliverables.
  • Stay informed on industry developments and help bring new technologies and modern manufacturing approaches into the project.


Interested? For this role we're looking for the following education, experience and skills

  • Degree in a relevant scientific or engineering field, or equivalent experience in biopharmaceutical manufacturing.
  • Experience in biopharmaceutical operations and large-scale drug substance or purification projects within the pharmaceutical industry.
  • Strong knowledge of mammalian biopharmaceutical production, buffer preparation, process operations and supporting digital tools and systems.
  • Ability to communicate clearly, write technical documentation and collaborate effectively across functions and stakeholder groups.
  • Experience working in regulated manufacturing environments, including inspections, audits and compliance-focused decision-making.
  • Willingness to adapt to project variabilities and a rapidly evolving work environment
  • Fluent in English; French is an advantage.
  • Occasional travel to the United States may be required during conceptual design and basic design phases.


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!

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

About UCB

UCB is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology. UCB aims to be the patient-preferred biotech leader by delivering medicines and solutions that improve lives. The company is headquartered in Brussels, Belgium, with approximately 7,500 employees in over 40 countries. UCB is listed on Euronext Brussels (symbol: UCB).
Learn more about UCB
Size
8,561 employees
Industry
Founded
1928
NASDAQ

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