MAKE YOUR MARK FOR PATIENTS

To strengthen our Pharma & Injectable Pharma department we are looking for a talented profile to fill the position of: QA Officer Injectable Manufacturing– Braine l’Alleud, Belgium

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
• Extensive experience in the pharmaceutical sector within QA, with experience in injectables being a major advantage
• Fluent English and French communication (oral and written)
• Fact-based decision-making process, accountability and delivering attitude
• Excellent interpersonal relationship skills
• Well-developed sense of discretion and ethics
• Excellent team player attitude
• Stress resistant, able to make quality/compliance decisions in a business environment
  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 around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

ABOUT THE ROLE

Your duties will ensure that local technical operations related to the manufacturing of injectable pharmaceutical products comply with applicable national and international regulations and guidelines (GMP), as well as relevant UCB Quality Policies. Additionally, you will oversee that marketed injectable pharmaceutical products are manufactured and supplied in accordance with UCB Product Quality Standards. You will proactively help operations identify, develop, and implement quality and operational excellence improvements in response to business requirements, technical changes, and regulatory requirements.

WHAT YOU WILL DO

Participation to product life cycle management

• Technology Transfer
• Process validation
• Equipment qualification
• Cleaning validation
• Stability studies
• Filing submission preparation and follow up of RA commitments
• Authoring and follow up of Product Quality Review/Continuous Process Verification

Participation to continuous improvement

• Review/approval of Change control, Failure investigation, Deviations, CAPA plans
• Participation to shopfloor oversight: shopfloor/ tier meeting presence, housekeeping tours, Quality oversight (witnessing/assessing the aseptic techniques)
• Review and authorization of relevant SOP
• Provide support in the preparation and execution of internal / external audits.
• Assist Manager to achieve team objectives
• Act as back up for other team QA Officers according to Manager instructions