Analyst Clinical Bioprocess Analytics
Il y a 2 jours
Brainel'Alleud, Wallonia, Belgique
UCB
Temps plein
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Make your mark for patients
We are looking for an Analyst in Clinical Bioprocess Analytics who is Collaborative, Curious, and Care-focused to join our Biological Method Development Sciences team, based at our UCB offices in Braine-l’Alleud, Belgium.
About the role
You will help ensure reliable analytical support for biologics manufacturing activities that ultimately contribute to patient solutions. Working at the intersection of science and operations, you will provide analytical expertise during manufacturing campaigns, support innovative technologies and foster high-quality data generation. You will also contribute to documentation governance, supporting procedures, process documentation and change management activities in partnership with project teams. You will help transform scientific excellence into meaningful patient impact. Who you will work with You will join a collaborative community within Biological Method Development Sciences and work closely with manufacturing, quality, development, and laboratory teams. Together, you will foster reliable analytical operations, knowledge sharing, and continuous improvement. You will also collaborate with external partners when supporting technology transfers and validation activities. The team values curiosity, mutual support and scientific excellence to help deliver high-quality outcomes for patients. What you will do
• You will provide analytical support during biologics manufacturing campaigns.
• You will deliver timely in-process monitoring and control results.
• You will manage sample coordination, equipment support, and troubleshooting activities.
• You will foster implementation of innovative analytical technologies and processes.
• You will support document creation, updates, and change controls collaboratively.
• You will support inspections, audits, and quality compliance requirements. Interested?
• Bachelor's or Master's degree in a scientific discipline.
• Experience managing controlled documentation within regulated environments.
• Expertise supporting procedure creation, revision, and document lifecycle activities.
• Experience coordinating change controls with cross-functional project teams.
• Strong practical experience with chromatography, electrophoresis, immunoassays, molecular techniques, or spectroscopy.
• Collaborative communication skills with curiosity for continuous improvement. Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities. 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, this role is hybrid with 40% of your time spent in the office, irrespective of your current contractual agreement. Should your current working arrangements differ, please contact your Talent Partner to discuss, before submitting your application. 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. Requisition ID: 94112 Recruiter: Gauthier Izambert Hiring Manager: Kevin Bernard Talent Partner: Caroline Lonchay Job Level: A Please consult HRAnswers for more information on job levels.
About the role
You will help ensure reliable analytical support for biologics manufacturing activities that ultimately contribute to patient solutions. Working at the intersection of science and operations, you will provide analytical expertise during manufacturing campaigns, support innovative technologies and foster high-quality data generation. You will also contribute to documentation governance, supporting procedures, process documentation and change management activities in partnership with project teams. You will help transform scientific excellence into meaningful patient impact. Who you will work with You will join a collaborative community within Biological Method Development Sciences and work closely with manufacturing, quality, development, and laboratory teams. Together, you will foster reliable analytical operations, knowledge sharing, and continuous improvement. You will also collaborate with external partners when supporting technology transfers and validation activities. The team values curiosity, mutual support and scientific excellence to help deliver high-quality outcomes for patients. What you will do
• You will provide analytical support during biologics manufacturing campaigns.
• You will deliver timely in-process monitoring and control results.
• You will manage sample coordination, equipment support, and troubleshooting activities.
• You will foster implementation of innovative analytical technologies and processes.
• You will support document creation, updates, and change controls collaboratively.
• You will support inspections, audits, and quality compliance requirements. Interested?
• Bachelor's or Master's degree in a scientific discipline.
• Experience managing controlled documentation within regulated environments.
• Expertise supporting procedure creation, revision, and document lifecycle activities.
• Experience coordinating change controls with cross-functional project teams.
• Strong practical experience with chromatography, electrophoresis, immunoassays, molecular techniques, or spectroscopy.
• Collaborative communication skills with curiosity for continuous improvement. Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities. 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, this role is hybrid with 40% of your time spent in the office, irrespective of your current contractual agreement. Should your current working arrangements differ, please contact your Talent Partner to discuss, before submitting your application. 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. Requisition ID: 94112 Recruiter: Gauthier Izambert Hiring Manager: Kevin Bernard Talent Partner: Caroline Lonchay Job Level: A Please consult HRAnswers for more information on job levels.