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External Manufacturing Operations Associate
View: 150
Update day: 13-11-2025
Location: Braine-l’Alleud Walloon Brabant
Category: R & D IT - Software
Industry: Pharmaceutical Manufacturing
Position: Entry level
Job type: Full-time
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Job content
Make your mark for patients.We’re here because we want to build the future and transform patients’ lives for the better.At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?The External Manufacturing Operations Associate function is also a steppingstone to the role of EMO Lead. He / she could be asked to manage the operational relationships between UCB and the least troublesome CMO’s and Vendors.In This Context, Your Main Accountabilities Will Be- Support EMO Leads in the creation and management of Change Controls (CC) related to CMO’s. After some time, the support lead should autonomously handle most of the CC process. Including:
- Understanding the business need and create a first draft of the CC using UCB’s templates.
- Identify the proper stakeholders.
- Use UCB’s document management system to manage modifications to the CC in draft mode.
- Stakeholders’ management within the set deadlines before asking to join the correct Change Control Committee.
- May defend the CC in front of the CCC with the help of the EMO Lead/Vendor teams.
- Once approved by the CC Board, input the actions in UCB’s Quality Management System and assign them to the proper stakeholders.
- Follow-up the actions to ensure that they are accomplished within the set deadlines
- Support EMO Leads in the management of deviations where the root cause and/or CAPAs have already been identified and put in place. Tasks include transferring the PR into UCB’s Quality Management System and following up on any pending actions.
- Double check Qualification and Validation Reports to spot errors or any other relevant reports coming from CMO’s or Vendors.
- Ensure that all changes to MBRs are documented in the change log.
- Contact and follow-up CMO’s or Vendors about the yearly Green Surveys or any other surveys. Assist them if they need help to fill them in and compile the results.
- Encode CMO KPI’s in Quickscore.
- Operational Management Reviews: assist the slide preparation if requested by an EMO Lead.
- Ad-hoc support on various EMP Projects: CoGs reduction, Process improvements, Digitalization, …
- Master’s Degree preferred in Chemical Engineering or related fields.
- At least 2 years of experience in a relevant operational management GMP environment.
- Experience in Pharma Project Management.
- Technical knowledge / expertise in the related focus areas.
- Very good command in English (both written & spoken). Good command in French is a strong asset.
- Being motivated and having the willingness to learn and develop within the team.
- Able to influence others, hold teams accountable, results orientated.
- Able to manage external business partners.
- Strong communication and networking skills with both external and internal partners.
- Strong both analytical and conceptual thinking.
- Fully self-supported.
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Deadline: 28-12-2025
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