Position: Mid-Senior level

Jobtyp: Full-time

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Jobinhalt

Make your mark for patientsWe are looking for a Data Integrity & Documentation Control Improvement Officer who has strong analytical, communication and problem-solving skills to join us in our QA operations team, based in our Braine-l’Alleud office in Walloon Brabant, Belgium.About The RoleThe successful candidate will be responsible for ensuring data integrity and maintaining documentation control to support continuous improvement initiatives:
  • Ensure data integrity and compliance with regulatory requirements and industry best practices.
  • Develop and implement documentation control processes and procedures to support continuous improvement initiatives.
  • Collaborate with cross-functional teams, including GQA and IT experts, to identify areas for improvement and implement effective solutions.
  • Develop and maintain data governance at the site.
Who You’ll Work WithYou will interact with a large panel of stakeholders with your main interactions being with the QA operations departments employees and IT staff.What You’ll Do
  • When required, review and analyze data to ensure accuracy, completeness, and compliance with regulatory requirements.
  • Develop, implement, and maintain coherent documentation control processes and procedures, including document creation, review, approval, distribution, and archiving.
  • Collaborate with cross-functional teams to identify areas for improvement and implement effective solutions.
  • Provide training and support to team members on data integrity and documentation control best practices.
  • Monitor and report on key performance indicators related to data integrity and documentation control.
  • Perform data integrity and documentation audits at the site
  • Participate in internal and external audits as needed.
Interested? For this role we’re looking for the following education, experience and skills
  • Master or bachelor’s degree in a relevant field (e.g., Life Sciences, Engineering, or Quality Management).
  • Minimum of 3 years of experience in data integrity and documentation control within the biopharmaceutical industry.
  • Familiarity with regulatory requirements and industry best practices related to data integrity and documentation control.
  • Strong analytical and problem-solving skills.
  • Excellent attention to detail and accuracy.
  • Strong communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Proficient in Microsoft Office Suite and document management systems.
  • You are fluent in French and have a very good level in English
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 UsUCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.Why work for 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 equitable 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.Learn more about sustainability at UCB and how it is integrated into our business approach.UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.
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Frist: 20-01-2026

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